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BIOLOGY

CONCEPTS & CONNECTIONS


Fourth Edition

Neil A. Campbell • Jane B. Reece • Lawrence G. Mitchell • Martha R. Taylor

CHAPTER 28
Nervous Systems

Modules 28.1 – 28.9

From PowerPoint® Lectures for Biology: Concepts & Connections


Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
Homeostasis

Control the internal condition near constants


In mammal, homeostasis involve:
• Core body temperature
• Metabolic waste
• Blood pH
• Blood glucose concentration
• Blood water potential (osmotic pressure)
• The respiration gas concentration

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Homeostasis Control

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Koordinasi

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Stuktur dan Fungsi Sistem saraf

Sistem saraf menerima input sensoris,


mengolahnya, dan mengirimkan perintah
tertentu

• Sistem saraf memiliki tiga fungsi yang


berkaitan
– Menerima rangsang
– Mengintegrasikan
– Memberikan perintah

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SENSORY INPUT

INTEGRATION
Sensory receptor

MOTOR OUTPUT

Brain and spinal cord

Effector
Peripheral nervous Central nervous
system (PNS) system (CNS)

Figure 28.1A

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• Sistem saraf dapat dibagi menjadi dua defisi

– Sistem saraf pusat, terdiri dari otak dan sum-


sum tulang belakang
– Sistem saraf tepi terdiri dari saraf dan ganglion
yang membawa sinyal masuk dan keluar dari
sistem saraf pusat

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Sistem saraf pusat dan sistem saraf tepi pada
manusia
CENTRAL NERVOUS PERIPHERAL
SYSTEM (CNS) NERVOUS
SYSTEM (PNS)
Brain
Cranial
nerve
Spinal cord

Ganglia
outside
CNS
Spinal
nerves

Figure 28.11A

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• Terdapat tiga jenis neuron berkaitan dengan
tiga fungsi utama sistem saraf
– Neuron sensori membawa sinyal dari daerah
reseptor ke sistem saraf pusat
– Interneuron mengintegrasikan data dan
mengalirkan sinyal
– Neuron motoris mengalirkan sinyal ke efektor

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1 Sensory
receptor 2 Sensory neuron

Brain

Ganglion

3
Motor
neuron Spinal
cord
Quadriceps 4
muscles

Interneuron

CNS
Nerve
Flexor
muscles
PNS

Figure 28.1B

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Neuron
Signal direction Dendrites

Cell body
Cell
body

Node of Ranvier

Myelin sheath

Signal
Axon pathway
Schwann cell
Nucleus
Nucleus Nodes of
Ranvier Schwann cell

Myelin sheath Synaptic knobs

Figure 28.2

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Sinyal saraf dan proses hantarannya
Neuron menjaga beda potensial pada
membran sel

• Potensial istirahat dari membran sel


disebabkan oleh kemampuan membran sel
untuk mempertahankan Voltmeter
Plasma

– Muatan positif
membrane Microelectrode
–70 mV outside cell

diluar sel Microelectrode


inside cell

– Muatan negatif
di daerah sitoplasma Axon

Neuron

Figure 28.3A
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• Potensial istirahat dihasilkan dan dipertahankan
dengan bantuan pompa Na-K
– Pompa ini membawa K+ masuk ke dalam sel dan Na+
keluar sel
OUTSIDE OF CELL
K+ Na+ K+ Na+
Na+
Na+ Na+
Na+ Na+ Na+
Na+ Na+
Na+
Na+ Na+
channel

Plasma K+
Na+ - K+
membrane pump

K+
channel
Na+ K+
K+ K+
Protein
K+ K+
K+
K+
K+
K+ K+
INSIDE OF CELL

Figure 28.3B

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Sinyal pada sistem saraf dimulai akibat
adanya perubahan pada potensial membran
• Rangsang mengubah permeabilitas membran sel
– Ion melintasi mebran sel, merubah potensial membran
– Ini mengakibatkan terbentuknya sinyal saraf

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Graded
potential

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Potensial Aksi

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Potensial aksi disebabakan oleh
membukanya voltage gate chanel
akibat depolarisasi pada membran
sel memcapai ambang

Terdapat dua voltage gate


chanel:
Na voltage gate chanel:
membuka terlebih dahulu
K voltage gate chanel
membuka kemudian

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Na+
K+

Na+
3 Additional Na+ channels open, K+
K+ channels are closed; interior of 4 Na+ channels close and
cell becomes more positive. inactivate. K+ channels
open, and K+ rushes
Na+
Action out; interior of cell more
potential negative than outside.
3

4
2 5 The K+ channels close
Na+ Threshold
potential relatively slowly, causing
2 A stimulus opens some Na+ 1 1 a brief undershoot.
channels; if threshold is reached, 5
action potential is triggered. Resting potential

Neuron
Neuron
interior
interior
1 Resting state: voltage gated Na+
and K+ channels closed; resting
potential is maintained. 1 Return to resting state.

Figure 28.4

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Potensial aksi di satu titik menginduksi
terjadinya potensial aksi di titik lain
Axon

Action potential

Axon
1 Na+ segment

K+ Action potential

2 Na+

K+
K+ Action potential

3 Na+

K+ Figure 28.5

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• Kenapa hantaran rangsang terjadi satu arah?
• Manakah yang lebih cepat menghantarkan
rangsang: sel saraf bermielin atau tidak
bermielin? Kenapa?
• Manakah sel saraf yang lebih cepat
menghantarkan rangsang: sel saraf dengan
akson berdiameter besar atau sel saraf dengan
akson berdiameter kecil?

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• Kecepatan hantaran rangsang ditentukan oleh
perbandingan kecepatan difusi Na disepanjang akson
(NaL) dengan difusi Na pada membran sel (NaT)
– Kecepatan hantaran rangsang makin cepat jika NaL/NaT
makin besar. Ini dapat dilakukan dengan
• Memperbesar ukuran sel saraf
• Menurunkan permeabilitas membran sel terhadap Na
(solusinya dengan menambahkan membran mielin)

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Penghantaran rangsang satu arah disebabkan oleh adanya
periode refraktori
Periode refraktori juga membratasi frekuensi terjadinya
potensial aksi

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Sel saraf berkomunikasi satu sama lain
melalui sinaps
• Sinaps merupakan elemen kunci dalam sistem saraf
– Ini merupakan hubungan atau titik hantaran antara dua
sel saraf atau antara sel saraf dengan sel efektor

• Sinap dapat berupa sistem elektrik atau kimia


– Pada sinaps elektrik, potensial aksi langsung
dihantarkan dari sel ke sel. (ini terjadi karena adanya gap
juntion pada hubungan antar sel)
– Pada sinaps kimia, neurotansmiter dilepaskan pada
celah sinaps dan berikatan pada reseptornya di sel pos
sinaps

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TIGHT
JUNCTION

ANCHORING
JUNCTION

COMMUNICATING JUNCTION/GAP JUNTION

Plasma
membranes of
adjacent cells

Extracellular
Figure 4.19B matrix

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SENDING 1
NEURON
Action
Axon of Vesicles potential
sending
arrives
neuron Synaptic
knob SYNAPSE

2
3
Vesicle fuses with
plasma membrane Neurotransmitter
is released into
synaptic cleft

SYNAPTIC
CLEFT
4
Receiving
neuron Neuro-
transmitter
RECEIVING Neurotransmitter binds to
NEURON
Ion channels molecules receptor

Neurotransmitter Neurotransmitter broken


Receptor down and released

Ions

5 Ion channel opens 6 Ion channel closes Figure 28.6


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Sinap kimia memungkinkan terjadinya
pemrosesan informasi yang kompleks

• Neurotransmiter eksisatorik memicu terjadinya


potensial aksi pada sel posinap
• Neurotransmiter inhibitorik menurunkan
kemampuan sel posinap untuk membentuk
potensial aksi
• Penjumlahan antara efek eksisatorik dan
inhibitorik menentukan apakah sel saraf akan
menghantarkan sinyal atau tidak

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• Sel saraf
Dendrites Synaptic knobs

mungkin
menerima
sinyal dari
ratusan sel
Myelin
sheath
Receiving

saraf lainnya cell body

Axon
Synaptic
knobs

Figure 28.7

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Otot

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Energi kontraksi

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BIOLOGY
CONCEPTS & CONNECTIONS
Fourth Edition

Neil A. Campbell • Jane B. Reece • Lawrence G. Mitchell • Martha R. Taylor

CHAPTER 26
Chemical Regulation

Modules 26.1 – 26.5

From PowerPoint® Lectures for Biology: Concepts & Connections


Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
Karakter dari regulasi secara kimia
Sinyal kimia mengatur fungsi tubuh

• Kelenjar endokrin dan sel neurosekretori


memproduksi hormon
– Hormon merupakan sinyal kimia yang dibawa oleh
darah dan menyebabkan perubahan spesifik pada sel
target

• Semua sel yang mensekresikan hormon masuk ke


dalam sistem endokrin
– Sistem ini bekerja sama dengan sistem saraf untuk
mengatur aktivitas tubuh

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Komunikasi sel

Figure 26.1B

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Amplifikasi sinyal

Figure 26.2A
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Sistem endokrin pada vertebrata
Overview: Sistem endokrin pada vertebrata

• Sistem endokrim pada vertebrata terdiri lebih dari


12 kelenjar
– Kelenjar-kelenjar tersebut mensekresikan lebih dari 50
hormon

• Hanya kelenjar sek dan korteks adrenal yang


menghasilkan hormon steroid

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Table 26.3, part 2

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Hipothalamus merupakan penghubung antara
sistem saraf dan endokrin

• Hipotalamus
merupakan pusat
pengontrolan dari
sistem endokrin
– Kelenjar ini mengatur
sekresi dari anterior
dan posterior pituitari

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HORMONES dan HOMEOSTASIS
Tiroid mengatur perkembangan dan
metabolisme

• Tiroid memproduksi dua hormon amine


– T4 and T3

– Keduanya mengatur perkembangan dan


metabolisme

• Mekanisme feedback negatif menjaga


keseimbangan kadar T4 dan T3 di darah

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• Ketidak seimbangan tiroid dapat
mengakibatkan kretinisme, gangguan
metabolisme, dan goiter
No inhibition
Hypothalamus

TRH

Anterior
pituitary

TSH
No iodine Insufficient
T4 and T3
Thyroid
produced

Thyroid grows
to form goiter

Figure 26.6A, B
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Hormon dari tiroid dan paratiroid berperan
mengatur keseimbangan kalsium

• Kadar kalsium di regulasi oleh keseimbangan


dari dua hormon yang bersifat antagonis
– calcitonin dari tiroid
– Parathormon dari kelenjar paratiroid

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• Calcium homeostasis
Calcitonin

Thyroid
gland
releases Stimulates Reduces
calcitonin Ca2+ deposition Ca2+ uptake
in bones in kidneys

STIMULUS:
Rising
blood Ca2+
level Homeostasis: Normal blood
(imbalance) STIMULUS:
calcium level (about 10 mg/100 mL)
Falling
blood Ca2+
level
(imbalance)

Active
vitamin D
Parathyroid
glands
release parathyroid
hormone (PTH)
Parathyroid
Stimulates Increases Increases gland
Ca2+ release Ca2+ uptake Ca2+ uptake
PTH
from bones in kidneys in intestines
Figure 26.7
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Kelenjar adrenal mengatur respon tubuh terhadap
stres

• Hormon dari kelenjar adrenal


mempertahankan keseimbangan tubuh dalam
keadaan stres
• Medula adrenal
– Sinyal saraf dari hipotalamus menstimulasi
sekresi dari epinefrin dan norepinefrin
– Kedua hormon ini memicu respon fight or flight

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• Korteks adrenal

– Sinyal kimia berupa ACTH menstimulasi sekresi


dari kortikosteroid, termasuk didalamnya
glukokortikoid dan mineralkortikoid
– Kortikosteroid mengakibatkan peningkatan
tekanan darah dan energi sebagai respon
terhadap stres jangka panjang

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• Proses kelenjar adrenal menangani stres

Adrenal
medulla STRESS

Adrenal Nerve
gland signals Hypothalamus
Adrenal
cortex
Kidney Releasing hormone
Nerve
Spinal cord Anterior pituitary
cell
(cross Blood vessel
section)
Nerve ACTH
cell

Adrenal ACTH Adrenal cortex


medulla

Epinephrine and Mineralocorticoids Glucocorticoids


norepinephrine

SHORT-TERM STRESS RESPONSE LONG-TERM STRESS RESPONSE

1. Glycogen broken down to glucose; 1. Retention of 1. Proteins and fats


increased blood glucose sodium ions broken down and
2. Increased blood pressure and water by converted to
kidneys glucose, leading to
3. Increased breathing rate increased blood
2. Increased
4. Increased metabolic rate blood volume glucose
5. Change in blood-flow patterns, leading and blood 2. Immune system
to increased alertness and decreased pressure may be
digestive and kidney activity suppressed
Figure 26.10
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BIOLOGY
CONCEPTS & CONNECTIONS
Fourth Edition

Neil A. Campbell • Jane B. Reece • Lawrence G. Mitchell • Martha R. Taylor

CHAPTER 21
Nutrition and Digestion

Modules 21.1 – 21.3

From PowerPoint® Lectures for Biology: Concepts & Connections


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Energi, molekul organic dan nutrisi esensial

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Overview: Pemrosesan makanan terjadi
dalam 4 tahapan

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Gastrovaskuler

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Saluran pencernaan

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Saluran pencernaan manusia

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Sistem pencernaan pada Manusia
Sistem pencernaan manusia terdiri dari
saluran pencernaan dan kelenjar asesoris

• Ketika makanan di telan makanan tersebut


akan bergerak disepanjang saluran pencernaan
melalui gerakan peristaltik
– Peristalsis merupakan kontraksi ritmis dari otot
pada dinding saluran pencernaan
– Otot berbentuk cincin (Spinhter) mengatur
pergerakan makanan

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Oral cavity
Mouth
Tongue Pharynx
Salivary
glands

Esophagus
Liver
Stomach

Pyloric
sphincter
Stomach
Gall-
bladder
Small
Pancreas intestine Small
intestine
Large
intestine

Rectum

Anus Figure 21.4

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Bolus of food
Tongue
Epiglottis Epiglottis
up down
Pharynx

Larynx
Esophageal Larynx Larynx
sphincter up down
Trachea
Esophagus Esophagus
(windpipe)

Sphincter contracted Sphincter relaxed Sphincter contracted

Figure 21.6

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Esofagus mendorong makanan masuk ke
dalam lambung

• Gerakan peristaltik mendorong makanan


masuk ke dalam lambung

Circular Relaxed
muscle layer muscles
Circular Relaxed
muscles muscles
contract,
Bolus of constricting
food passageway
and pushing
bolus down
Longitudinal
muscles
contract,
shortening
passageway
ahead of bolus

Stomach
Longitudinal
muscle layer

Figure 21.7

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Pencernaan lambung
Interior surface Pits
of stomach Gastric juice
(mucus, HCI,
Food particle and pepsinogen)
3
Epithelium
Gastric
juice Pepsinogen Pepsin (active
2 enzyme)
Mucous
cells HCI
Pyloric
sphincter
Gastric 1
STOMACH
gland Chief cells

Pariental cells

Figure 21.8

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Faktor yang mempengaruhi pengosongan lambung

• Osmolalitas, keasaman, dan kandungan kalori makanan


• Kondisi fisik makanan

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Usus kecil merupakan organ utama dalam
pencernaan secara kimia dan penyerapan nutrisi

• Cairan yang bersifat basa dari pankreas


menetralkan chyme yang masuk dari lambung
– Enzim di dalamnya mencerna polisakarida,
protein, asam nukleat, dan lemak

• Garam empedu mengemulsi lemak sehingga


lebih mudah dicerna oleh lipase pankreas
– Garam empedu dibuat oleh hati dan disimpan di
kantung empedu

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Table 21.10

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INTERIOR OF INTESTINE
Blood vessel
with blood Nutrient
en route to absorption
the liver
Nutrient
absorption
Microvilli

Epithelial
cells

Lumen
Muscle
layers
Blood
Circular folds capillaries

Villi Lymph EPITHELIAL


vessel CELLS
Nutrient
absorption

INTESTINAL WALL VILLI

Figure 21.10B

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Penyerapan lemak

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Distribusi nutrisi

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Usus besar berperan sebagai tempat
penyerapan air

• Material yang Large

tidak dicerna intestine


(colon)

masuk ke dalam
usus besar/kolon
– Air diserap End
of small Small
intestine intestine

– Feces Rectum

diproduksi Anus

Nutrient
flow
Appendix

Cecum
Figure 21.11

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Jenis makanan dan Adaptasi pencernaan
Adaptasi dari sistem pencernaan vertebrata
mencerminkan jenis makanannya

• Herbivora dan omnivora memiliki saluran


pencernaan yang lebih panjang dari karnivora
– Material pada tanaman lebih susah dicerna
daripada daging

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Small intestine

Small
intestine Stomach

Cecum

Colon
(large
intestine)

CARNIVORE HERBIVORE Figure 21.12A

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• Beberapa mamalia memiliki bakteri pencerna
selulosa di kolon atau sekumnya
– Sekum merupakan kantung tempat
terhubungnya usus besar dan kecil
– Contoh: kuda dan gajah

• Mamalia jenis lainya mencerna kembali


fesesnya untuk memperoleh kembali nutrien
– Contoh: kelinci dan beberapa jenis rodensia

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• Ruminansia memproses selulosa pada
lambung dengan empat ruang

Intestine 3 Omasum 1 Rumen

Esophagus

Rumen
4 Abomasum 2 Reticulum

Figure 21.12B
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BIOLOGY
CONCEPTS & CONNECTIONS
Fourth Edition

Neil A. Campbell • Jane B. Reece • Lawrence G. Mitchell • Martha R. Taylor

CHAPTER 23
Circulation

Modules 23.1 – 23.3

From PowerPoint® Lectures for Biology: Concepts & Connections


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Sistem sirkulasi berhubungan dengan semua
jaringan di dalam tubuh

• Kapiler merupakan pembuluh darah


mikroskopik
– Mereka membentuk jaring-jaring yang saling
berhubungan di jaringan

Capillary

Red
blood
cell

Figure 23.1A

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– Tidak ada substansi yang harus berdifusi keluar
atau masuk ke dalam sel dalam jarak yang jauh

Capillary

Diffusion of
INTERSTITIAL molecules
FLUID

Tissue
cell

Figure 23.1B

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Mekanisme trasportasi internal
Beberapa tipe transportasi internal berevolusi
pada hewan

• Pada Cnidaria dan cacing


pipih, rongga
gastrovaskuler berfungsi
sebagai tempat
pencernaan sekaligus
transportasi
Mouth

Circular
canal

Figure 23.2A

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Figure 23.2B

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Sistem kardiovaskuler pada mamalia
Jantung manusia dan sistem kardiovaskulernya
serupa dengan semua mamalia

• Mamalia memiliki dua artrium dengan dinding


tipis dan berfungsi memompa darah ke
ventrikel
– Ventrikel dengan dinding yang tebal memompa
darah keseluruh organ di dalam tubuh

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Pulmonary Aorta
artery

Pulmonary
Superior
artery
vena cava
LEFT
ATRIUM
RIGHT
ATRIUM

Pulmonary
veins Pulmonary
veins

Semilunar
Semilunar
valve valve

Atrioventricular
valve Atrioventricular
valve

Inferior
vena cava

RIGHT LEFT
VENTRICLE VENTRICLE
Figure 23.4A

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Superior 7
Capillaries of
vena cava
Head and arms

Pulmonary
artery Pulmonary
artery
Capillaries Capillaries
of right lung 9 Aorta of left lung

3 2 3

4
11
Pulmonary Pulmonary
vein vein
5
1 LEFT ATRIUM
RIGHT ATRIUM
10 LEFT VENTRICLE
RIGHT VENTRICLE

Inferior Aorta
vena cava

Capillaries of
abdominal organs
and legs
8
Figure 23.4B

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Struktur dari pembuluh darah sesuai dengan
fungsinya

• Satu lapis sel membentuk dinding dari


pembuluh kapiler
• Arteri dan vena memiliki otot polos dan
jaringan ikat
– Katup mencegah aliran balik pada vena

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Valve
Epithelium Basement
membrane
Epithelium
Epithelium
Smooth
muscle Smooth
CAPILLARY muscle
Connective Connective
tissue tissue

ARTERY VEIN

VENULE
ARTERIOLE

Figure 23.5

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Jantung kontraksi dan relaksasi secara ritmik

• Diastole
1 Heart is 2 Atria
– Darah mengalir dari relaxed.
AV valves
contract.

vena ke runga are open.

jantung
• Sistol
SYSTOLE
– Artrium berkontraksi
0.1 sec

singkat dan mengisi 0.3 sec


3 Ventricles
ventrikel dengan darah 0.4 sec
contract.
Semilunar
valves
– Kemudian ventrikel are open.

kontraksi dan DIASTOLE


mendorong darah
keluar
Figure 23.6

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• Katup pada jantung mencegah terjadinya aliran
balik
• Kardiak output
– Jumlah darah yang dipompa oleh ventrikel kiri
ke aorta tiap menitnya

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
Pacemaker mengatur tempo dari detak jantung

• SA node (pacemaker) menghasilkan sinyal


elektrik yang memicu kontraksi atrium
• AV node kemudian mengalirkan sinyal ke
centrikel
Specialized
Pacemaker AV node
muscle fibers
(SA node)

Right
atrium

Right
ventricle
1 2 3 4

ECG Figure 23.7

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Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
Darah menghasilkan tekanan ke pembuluh darah

• Tekanan darah tergantung pada


– cardiac output (stroke volum X laju detak
jantung)
– Resistensi dari pembuluh darah (diameter,
panjang, elastisitas pembuluh darah)

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• Tekanan Systolic
pressure

terbesar Diastolic
terjadi di pressure

arteri Relative sizes and


numbers
– Menjadi nol of blood
vessels
pada saat
darah
mencapai
vena

Figure 23.9A

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• Tiga faktor yang menjaga aliran darah balik ke
jantung
– Kontraksi otot
– Pernafasan
– Katup yang terbuka satu arah

Direction of
blood flow
in vein

Valve (closed) Valve (open)


Skeletal muscle Figure 23.9B

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Otot polos mengatur distribusi darah

• Kontraksi otot pada arteri dan spinchter


mengatur aliran darah melalui kapiler

Precapillary sphincters Thoroughfare Thoroughfare


channel channel

Arteriole Venule Arteriole Venule


Capillaries

1 Sphincters relaxed 2 Sphincters contracted


Figure 23.11

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Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
Kapiler memungkinkan transfer substansi
melalui dindingnya

Figure 23.12A

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• Transfer material antara darah dengan cairan
intertistisial terjadi akibat
– Perembesan melalui celah pada dinding kapiler
– Difusi melalui dinding kapiler
– Adanya tekanan darah
– Adanya tekanan osmotik

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Tissue cells

Osmotic Osmotic
Arterial pressure pressure Venous
end of end of
capillary capillary

Blood Blood
pressure pressure

INTERSTITIAL
FLUID NET PRESSURE NET PRESSURE
OUT IN

Figure 23.12B

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Struktur dan fungsi darah
Darah terdiri dari sel yang terbenan di dalam plasma

• Plasma merupakan komponen cair yang terdiri


dari berbagai substansi

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Withdraw
blood
Centrifuge
Place in tube
PLASMA 55%
CONSTITUENT MAJOR FUNCTIONS CELLULAR ELEMENTS 45%

Solvent for CELL TYPE NUMBER FUNCTIONS


Water carrying other (per mm3 of blood)
substances
Erythrocytes
Salts (red blood cells) 5–6 million Transport of
Sodium Osmotic balance, oxygen
Potassium pH buffering, and (and carbon
Calcium regulation of dioxide)
Magnesium membrane
Chloride permeability Leukocytes
Bicarbonate Defense and
(white blood cells) 5,000–10,000 immunity
Plasma proteins
Albumin Osmotic balance,
pH buffering Lymphocyte
Fibrinogen Clotting Basophil
Immunoglobins Immunity
(antibodies) Eosinophil
Substances transported by blood Monocyte
Nutrients (e.g., glucose, fatty acids, vitamins) Neutrophil
Waste products of metabolism
Respiratory gases (O2 and CO2) Platelets 250,000–
Hormones Blood clotting
400,000

Figure 23.13

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Sel darah merah berperan dalam trnasportasi
oksigen

• Sel darah merah


mengandung hemoglobin
– Hemoglobin mampu
mengangkut O2

Figure 23.14

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Sel darah putih membantu melindungi tubuh

• Sel darah putih bekerja di dalam dan di luar


sistem sirkulasi
– Mereka melawan infeksi dan kanker

Basophil Eosinophil

Monocyte

Neutrophil Lymphocyte

Figure 23.15

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Pembekuaan darah membentuk sumbatan ketika
pembuluh darah mengalami pelukaan

• Ketika pembuluh
darah rusak, platelet
merspon
– Mereka membantu
pembentukan fibrin
yang berperan
dalam proses
penyumbatan

Figure 23.16B

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1 Injury to lining of blood 2 Platelet plug forms 3 Fibrin clot traps
vessel exposes connective blood cells
tissue; platelets adhere

Connective
tissue
Platelet
Platelet releases chemicals plug
that make nearby platelets sticky

Clotting factors from:

Platelets Calcium and


other factors
Damaged cells in blood plasma

Prothrombin Thrombin

Fibrinogen Fibrin

Figure 23.16A

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


BIOLOGY
CONCEPTS & CONNECTIONS
Fourth Edition

Neil A. Campbell • Jane B. Reece • Lawrence G. Mitchell • Martha R. Taylor

CHAPTER 22
Respiration: The Exchange of
Gases

Modules 22.1 – 22.4

From PowerPoint® Lectures for Biology: Concepts & Connections


Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
Mekanisme pertukaran gas

• Pertukaran gas merupakan pertukaran antara


organisme dengan lingkungannya
– Ini dikenal juga dengan respirasi

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Overview: Pertukaran gas membutuhkan
pernafasan, transportasi gas, dan
pelepasan/pengambilan gas di jaringan

• Pertukaran gas merupakan hal yang esensial


karena metabolisme membutuhkan O2 dan
menghasilkan CO2
• Terdapat tiga fase pertukaran gas

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O2

Lung CO2

1 Breathing

Circulatory
system

2 Transport
of gases by
the circulatory
system

Mitochondria

3 Servicing of O2
cells within
the body CO2
tissues
Capillary

Cell
Figure 22.1

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Hewan melakukan pertukaran O2 dan CO2 pada
daerah permukaan tubuh yang lembab

• O2 masuk ke tubuh hewan dan CO2 keluar dari


tubuh, keduanya mengalir secara difusi melalui
permukaan pernafasan
– Permukaan pernafasan di bangun oleh sel hidup

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• Pada sebagian besar hewan, bagian tubuh yang
terspesialisasi berperan sebagai tempat
pertukaran gas
– Gills in fish

Body surface

Respiratory
surface
(gill)

CO2 Capillaries

O2
Figure 22.2B

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– Tracheae in – Lungs in land
insects vertebrates

Body surface
Body surface

Respiratory
surface Respiratory
(tracheae) surface
O2 (within lung)

Body cells CO2 O2 Capillary


(no capillaries)
CO2

Figure 22.2C, D

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Insang teradaptasi untuk pertukaran gas di
lingkungan perairan

• Insang merupakan perpanjangan dari tubuh


yang berperan menyerap O2 dari air
• Pada ikan, filamen insang memiliki banyak
lamela
– Lamellae dikemas bersamaan dengan pembuluh
darah
– Mereka merupakan permukaan pernafasan

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Gill arch

• The structure Direction

of fish gills
of water
flow

Gill arch

Blood
vessels

Gill
filaments
Oxygen-poor
blood

Oxygen-rich
blood

Lamella

Water
flow Figure 22.3

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Countercurrent pada insang meningkatkan
penyerpan O2

• Aliran darah pada


lamela berlawanan arah
dengan aliran air
Water flow

– Sistem countercurrent over


lamellae

menjaga gradien yang


memaksimumkan
penyerapan O2

Blood flow
through
lamellae

Figure 22.4

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


BIOLOGY
CONCEPTS & CONNECTIONS
Fourth Edition

Neil A. Campbell • Jane B. Reece • Lawrence G. Mitchell • Martha R. Taylor

CHAPTER 22
Respiration: The Exchange of
Gases

Modules 22.5 – 22.9

From PowerPoint® Lectures for Biology: Concepts & Connections


Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
Sistem trakea pada serangga memberikan pertukaran
secara langsung antara sel dengan udara

• Hewan darat melakukan petukaran gas dengan


udara yang di hirupnya
– Udara mengandung lebih banyak O2 dan
bergerak lebih mudah dari air
– Tetapi kehilangan cairan dari permukaan
pernafasan dapat menjadi masalah

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• Pada serangga, jaring-jaring trakea mengambil
fungsi pertukaran gas
– O2 berdifusi dari cabang trakea yang
membentuk tabung ke sel

Figure 22.5B

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Air sacs

Tracheae

Opening
for air

Body
cell

Tracheole Air
sac

Trachea

Air Body wall Figure 22.5A, C

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Vertebrata teresterial memiliki paru-paru

• Pada manusia dan mamalia, udara masuk


melalui rongga nasal
– Udara bergerak melalui faring dan laring
menuju ke trakea
– Trakea bercabang membentuk dua bronkus
– Setiap bronkus bercabang menjadi bronkiolus

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• The human respiratory system

Nasal
cavity

Pharynx
(Esophagus)
Left lung
Larynx
Trachea

Right
lung
Bronchus

Bronchiole

Diaphragm
(Heart)
Figure 22.6A

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• Ujung bronkiolus membentuk
kumpulan kantung yang
disebut dengan alveoli
– Alveoli membentuk permukaan
respirasi paru-paru Figure 22.6C

– Oksigen berdifusis Oxygen-rich


blood Oxygen-poor

melalui dinding tipis


blood

dari alveoli ke darah Bronchiole

Alveoli

Blood capillaries
Figure 22.6B

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Pernafasan memberikan pertukaran udara
pada paru-paru
• Pernafasan merupakan pergiliran dari inhalasi
dan ekhalasi

Rib cage
Rib cage
expands as
gets smaller
rib muscles Air Air
as rib muscles
contract inhaled exhaled
relax

Lung

Diaphragm

INHALATION EXHALATION
Diaphragm contracts Diaphragm relaxes
(moves down) (moves up)
Figure 22.8A

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• Kapasitas vital merupakan volume maksimum
dari udara yang dapat dihirup dan dikeluarkan
– Akan tetapi paru-paru kita dapat menampung
udara lebih banyak dari itu
– Alveolus tidak benar-benar mengempis
– Udara residu masih tetap di paru-paru setelah
proses ekhalasi

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Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
• Organisme lainnnya, sperti burung memiliki
kantung udara
– Kantung ini berperan sebagai tempat
penyimpanan udara dan menjaga aliran udara
satu arah pada paru-paru

Air Air
Anterior
air sacs

Trachea

Posterior Lungs Lungs


air sacs

Air
tubes
in lung
INHALATION: EXHALATION: 1 mn
Air sacs fill Air sacs empty; lungs fill
Figure 22.8B

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Pernafasan dikontrol secara otonom

• Pusat kontrol pernafasan terletak di pons dan


medula dari otak
– Sistem kontrol otomatis ini menjaga irama
pernafasan sesuai dengan kebutuhan tubuh

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• Selama olahraga, CO2 didalam darah
meningkat, menurunkan PH darah
– Ini memicu Brain

aliran Cerebrospinal fluid

kejadian
BREATHING CONTROL
CENTERS—stimulated by:

Pons

Medulla CO2 increase / pH decrease


in blood

Nerve signal
Nerve signals
indicating low
trigger
O2 level
contraction
of muscles

O2 sensor
in artery

Diaphragm
Figure 22.9 Rib muscles

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Transport gas di dalam tubuh
Darah mentransport gas, dengan hemoglobin
sebagai pembawa oksigen

• Jantung memompa darah miskin oksigen ke


paru-paru
– Di paru-paru oksigen diambil dan karbon
dioksida dilepaskan
– Dijaringan, darah mengambil CO2 dan
melepaskan O2
– Gas berdifusi sesuai dengan gradien
konsentrasinya di paru-paru dan jaringan
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• Gas exchange in
the body

Figure 22.10A

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


• Hemoglobin merupakan protein pada sel darah
merah
– Dia berperan membawa sebagian besar oksigen
di dalam darah

Heme Iron
group atom

O2 loaded O2
in lungs

O2 unloaded
in tissues O2

Polypeptide chain
Figure 22.10B

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Kenapa Hb dapat meningkatkan kemampuan
darah dalam mengangkut O2?

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Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
Beberapa faktor mempengaruhi kemampuan
Homoglobin dalam mengangkut Oksigen

1. pH darah
2. Keberadaan 1,2 dipospogliserat
3. Gradien konsentrasi O2 dan CO2
4. Suhu

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Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
Hemoglobin membantu transportasi CO2 dan
berperan sebagai buffer di darah

• Hemoglobin membentu menjaga kesetabilan


pH darah dan membawa sebagian CO2

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


• Sebagian besar CO2 di
TISSUE CELL

CO2 produced

darah bereaksi dengan


air membentuk asam INTERSTITIAL CO
FLUID 2

karbonat BLOOD
PLASMA CO2 Capillary

– Asam karbonat WITHIN


CAPILLARY
wall

dipecah menjadi H+ CO2

dan ion bikarbonat H2O

RED Hemoglobin
– H+ kemudian diikat BLOOD H2CO3
picks up
CELL Carbonic acid CO2 and H+

oleh hemoglobin, dan


ini membantu HCO3– + H+
Bicarbonate
menjaga kesetabilan
pH darah HCO3–
Figure 22.11A

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ALVEOLAR SPACE IN LUNG
• Sebagian besar CO2 di CO2

dalam darah ditrasport


dalam bentuk ion CO2

bikarbonat
CO2

CO2
H2O

Hemoglobin
H2CO3
releases
CO2 and H+

HCO3– + H+

HCO3–
Figure 22.11B

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


BIOLOGY
CONCEPTS & CONNECTIONS
Fourth Edition

Neil A. Campbell • Jane B. Reece • Lawrence G. Mitchell • Martha R. Taylor

CHAPTER 24
The Immune System

Modules 24.1 – 24.2

From PowerPoint® Lectures for Biology: Concepts & Connections


Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
Pertahanan non spesifik terhadap infeksi

Kulit, membran mukosa, sel fagositik, dan


protein antimikroba termasuk ke dalam
pertahanan non spesifik terhadap bakteri

• Sistem pertahanan pertama tubuh terhadap


infeksi bersifat non spesifik
– Mereka tidak membedakan antara agen
penginfeksi yang satu dengan agen pengionfeksi
yang lainnya

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• Makrofag berpatroli pada cairan intertistisial
– Mereka memakan bakteri dan sel terinfeksi
virus yang mereka temui

Figure 24.1A

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• Interferon diaktivasi oleh sel yang terinfeksi

VIRUS Viral nucleic acid


6 Antiviral proteins block
1
viral reproduction

2 Interferon New viruses


genes
turned on

mRNA
3 5 Interferon
stimulates
Interferon cell to turn
molecules on genes
for antiviral
proteins

HOST CELL 1 4 HOST CELL 2


Makes interferon; Protected against virus
is killed by virus by interferon from cell 1 Figure 24.1B

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Inflamasi memobilisasi pertahanan
nonspesifik
• Kerusakan jaringan memicu terjadinya respon
inflamasi

Skin surface Swelling


Pin

Phagocytes
Bacteria Phagocytes and
Chemical fluid move
signals into area
White
blood cell

1 Tissue injury; release of 2 Dilation and increased leakiness 3 Phagocytes (macrophages and
chemical signals such as of local blood vessels; migration neutrophils) consume bacteria
histamine of phagocytes to the area and cell debris; tissue heals

Figure 24.2

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


• Respon inflamasi dapat
– Menghilangkan infeksi pada jaringan
– Mencegah infeksi lebih lanjut

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Sistem limfatik merupakan komponen krusial
dalam melawan infeksi

• Sistem limfatik ,merupakan jejaring dari


pembuluh limfatik dan organ
– Dia mengembalikan cairan di jaringan ke
sistem peredaran
– Dia berperan melawan agen penginfeksi

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LYMPHATIC
Adenoid VESSEL
Tonsil
VALVE
Right lymphatic Tissue cells
duct, entering Lymph nodes
vein Interstitial
Thoracic duct, Blood
fluid
entering vein capillary
Thoracic
duct Thymus

Appendix LYMPHATIC
Spleen CAPILLARY

Masses of
lymphocytes and
macrophages

Bone
marrow Lymphatic
vessels

Figure 23.3

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


• Pembuluh limfatik mengambil cairan dari
jaringa.
• Ini akan dikembalikan ke darah dalam
bentuk cairan limfa
– Cairan limfa mengandung sedikit oksigen dan
nutrisi jika dibandingkan dengan cairan
intertistisial.
LYMPHATIC
VESSEL

VALVE
Tissue cells

Interstitial
Blood
fluid
capillary

LYMPHATIC
CAPILLARY Figure 23.3B

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


• Nodus limfa merupakan daerah kunci dari
pertahanan melawan infeksi
– Mereka dihuni oleh limfosit dan makrofag

Masses of
lymphocytes and
macrophages

Outer capsule of
lymph node

Macrophages

Lymphocytes

Figure 23.3C, D

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Immunitas spesifik
Respon immun yang bersifat spesifik

• Sistem immun merespon molekul asing yang


disebut dengan antigen
• Infeksi atau vaksinasi memicu respon immun
spesifik
• Immun sistem bereaksi terhadap antigen dan
mengingatnya

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Limfosit memiliki dua mekanisme pertahanan

• Terdapat dua tipe


BONE MARROW

limfosit yang Stem cell

berperan dalam
THYMUS

Via

respon immun blood

Immature
lymphocytes
– Sel B Antigen

mensekresikan receptors

antibodi yang B cell T cell

menyerang antigen
CELL-
HUMORAL Via MEDIATED
IMMUNITY blood IMMUNITY

– Sel T menyerang sel Lymph nodes,


spleen, and other
lymphatic organs Final
yang terinfeksi OTHER PARTS
OF THE
LYMPHATIC
maturation of
B and T cells

patogen Figure 24.5


SYSTEM in lymphatic
organ

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Antigen punya daerah spesifik yang dapat
dikenali oleh antibodi

• Determinan Antibody A

antigenik/epitop
molecules

Antigen-

merupakan binding
sites

bagian dari
antigen yang
dikenali oleh Antigen
Antigenic
determinants

antibodi

Antibody B
molecule

Figure 24.6

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Seleksi klonal berperan mengumpulkan
kekuatan untuk melawan antigen spesifik

• Ketika antigen masuk ke dalam tubuh, dia


hanya mengaktivasi limfoit dengan reseptor
yang komplementer dengannya
– Sel B dan T memperbanyak diri dan
berkembang menjadi sel efektor yang melawan
antigen pemicunya
– Proses ini disebut dengan seleksi klonal

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Antigen molecules

Variety of Antigen receptor


B cells in a (antibody on
lymph node cell surface)

Cell growth
division, and
differentiation

Clone of many Endoplasmic


effector cells reticulum
secreting
antibodies

Antibody
molecules

Figure 24.7

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Pada respon immun primer dihasilkan sel-sel
memori
• Pada respon immun primer, seleksi klonal
menghasilkan sel memori
– Sel-sel ini dapat memberikan immunitas
sepanjang hayat

Figure 24.8A

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


• Ketika sel
memori diaktifasi Unstimulated lymphocyte
oleh pendedahan First exposure to antigen

antigen, mereka
FIRST CLONE
memperbanyak
diri dengan cepat
Memory cells
dan Second exposure to antigen Effector cells

menghasilkan
SECOND CLONE
respon sekunder
yang cepat
More memory cells
New effector cells

Figure 24.8B

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Overview: Sel B merupakan komponen utama
dalam sistem immunitas humoral

• Dipicu oleh antigen spesifik, sel B


berdiferensiasi menjadi sel efektor
– Sel efektor ini disebut dengan sel plasma
– Sel plasma mensekresikan antibodi

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


PRIMARY RESPONSE Antigen
(initial encounter
with antigen) Antigen receptor
on a B cell
Antigen binding
to a B cell
Cell growth,
division, and
differentiation

Clone of
cells Memory B cell
Plasma cell
Antibody
molecules

Later
SECONDARY RESPONSE
exposure
(can be years later)
to same
Cell growth, antigen
division, and further
differentiation

Larger clone
of cells

Plasma cell
Memory B cell
Antibody Figure 24.9
molecules

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Antibodi merupakan senjata dalam
immunitas humoral

• Gambaran molekul antibodi

Figure 24.10A

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• Antibodi memiliki daerah pengikatan antigen
yang spesifik mengenali antigen yang memicu
sekresinya

Antigen-binding
sites

Light
chain

Heavy
chain

Figure 24.10B

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Terdapat lima jenis antibodi

• IgA
• IgG
• IgD
• IgM
• IgE

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Antibodi menandai antigen yang harus
dieleminasi
• Antibodi bekerja dengan cara
– Mencegah penempelan antigen berbahaya
– Mengkaugolasi bakteri atau virus
– Mempresipitasi antigen terlarut
– Mengaktifasi molekul komplemen

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Binding of antibodies to antigens
inactivates antigens by

Neutralization Agglutination Precipitation of Activation


(blocks viral binding sites; of microbes dissolved antigens of complement
coats bacterial toxins)
Complement
Bacteria
molecule
Virus

Antigen
Bacterium molecules
Foreign cell Hole

Enhances Leads to

Phagocytosis Cell lysis

Macrophage

Figure 24.11

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Sel T berperan dalam immunitas diperantarai
sel dan membantu sistem immunitas humoral

• Sel T helper dan sel T sitotoksik merupakan


komponen utama dalam immunitas yang
diperantarai sel
• Sel T helper juga memicu timbulnya respon
immun humoral

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
• Immunitas yang diperantarai sel
– Antigen Microbe
presenting sel
pertama-tama
Macrophage
1 (will become APC)

mempresentasik Antigen from microbe


(nonself molecule)

an antigen pada Self protein

sel T helper.
Antigen tersebut
Self protein
displaying
antigen T cell receptor
terikat molekul
MHC yang 2 3
Helper
Binding
site for

diproduksi oleh
self
T cell protein
4
APC Binding site
APC for antigen

Figure 24.13A
Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
• Reseptor sel T helper mengenali kompleks
antigen-MHC pada sel APC
– Interaksi tersebut mengaktivasi sel T helper
– Sel T helper kemudian dapat mengaktifasi sel
T sitotoksik dengan reseptor yang sama

Self protein Cell-mediated


displaying Cytotoxic
T cell Interleukin-2 immunity
an antigen T cell (attack on
receptor stimulates
cell division infected cells)

Interleukin-2
activates
APC Helper other T cells
T cell and B cells

Humoral
immunity
B cell (secretion of
antibodies by
Interleukin-1 plasma cells)
activates
helper T cell Figure 24.13B
Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
• Sel T sitotoksik berikatan dengan sel yang
terinfeksi dan menghancurkannya

1 Cytotoxic T cell binds 2 Perforin makes holes 3 Infected cell is destroyed


to infected cell in infected cell’s membrane

Hole
forming
Foreign
antigen
INFECTED CELL

Cytotoxic
Perforin T cell
molecule

Figure 24.13C

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Sel T sitotoksik juga berperan dalam melawan
kanker
• Sel T sitotoksik
mungkin sel kangker
– Protein permukaan
dari sel kanker
kemungkinan berbeda
dengan sel normal

Figure 24.14

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Kerja dari sistem immun kita sangat
tergantung dari kondisi genetik kita

• Respon immun umunya hanya akan


menyerang substansi yang berbeda dengan
molekul di dalam tubuh kita
– Dia umumnya akan menolak transplantasi
organ
– Sel-sel dari organ cangkokan tidak memiliki
protein unik yang dimiliki oleh resepien

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Gangguan pada sistem immun
Gangguan pada sistem immun dapat
menimbulkan penyakit
• Penyakit autoimmun
– Sistem immun menyerang molekul diri sendiri
• Penyakit immunodefisiensi
– Dapat disebabkan oleh kekurangan/
abnormalitas dari komponen immunitas, dan
dapat juga disebakan oleh infeksi
• Sters fisik dan emosi dapat juga menurunakan
kinerja sistem immunitas
Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
Allergies merupakan reaksi hipersensitif
terhadap antigen di lingkungan

• Alergi merupakan respon abnormal terhadap


alergen di lingkuangan

B cell
(plasma cell)
Histamine

Mast
Antigenic
cell
determinant

Antibodies Allergen binds to Histamine is


Allergen B cells make
(pollen grain) antibodies attach to antibodies on released, causing
mast cell mast cell allergy symptoms

SENSITIZATION: Initial exposure to allergen LATER EXPOSURE TO SAME ALLERGEN

Figure 24.17

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


BIOLOGY
CONCEPTS & CONNECTIONS
Fourth Edition

Neil A. Campbell • Jane B. Reece • Lawrence G. Mitchell • Martha R. Taylor

CHAPTER 25
Control of the Internal
Environment

Modules 25.1 – 25.4

From PowerPoint® Lectures for Biology: Concepts & Connections


Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
Termoregulasi
Panas diperoleh dan keluar dari tubuh melalui 4
cara
• Pengaturan suhu tubuh melibatkan
penyesuaian terhadap pertukaran panas
dengan lingkungan

Convection Radiation

Evaporation

Conduction Figure 25.1

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Termoregulasi tergantung pada panas yang
diprosuksi dan panas yang diperoleh atau
dilepas

• Baik hewan endoterm maupun ektoterm


mengubah laju kehilangan panasnya
• Hanya hewan endotermi yang akan mengubah
produksi panasnya akibat perubahan suhu
lingkungan

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


• Perubahan hormonal meningkatkan produksi
panas dengan cara meningkatkan laju
metabolisme
– Bulu dan rambut membantu tubuh menghindari
kehilangan panas
– Bergetar, seperti yang dilakukan lebah, juga
meningkatkan produksi panas dari proses metaboisme

Figure 25.2A

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


• Aliran darah melalui kulit mempengaruhi laju
kehilangan panas

Top view of shark


Skin
Blood vessels
of gills Artery

Vein

Capillary network
Heart within muscle

Artery and vein


under the skin Dorsal aorta

Figure 25.2B

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Body surface (cool)
• Pada sistem pertukaran
panas secara countercurrent, 18˚ 20˚
Darah dari sumbu tubuh C C

menghangatkan darah
dingin dari insang atau 20˚ 22˚
anggota gerak Blood
flow
– Proses ini dapat
22˚ 24˚
mencegah kehilangan
panas Heat
transfer
24˚ 26˚

Inner body (warm)

Figure 25.2C
Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
Perilaku sering mempengaruhi suhu tubuh

• Berjemur
• Berteduh
• Mandi
• Mengubur diri
• Migrasi

Figure 25.3

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Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
Menurunkan laju metabolisme berperan dalam
penyimpanan energi
• Torpor adalah peristiwa penurunan aktivitas
dan menurunakn laju metabolisme
– Hibernation
pada suhu
weather
– Estivation
pada suhu
tinggi

Figure 25.4

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Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
Pada manusia
kulit merupakan
salah satu
organ yang
pentin dalam
thermoregulasi

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
Osmoregulasi

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Manusia harus membuang sisa-sisa-atau produk
berbahaya dari proses metabolismenya.
• Senyawa bernitrogen merupakan produk sampingan dari
metabolisme tubuh yang sangat beracun. Senyawa
bernitrogen diproduksi dari metabolisme protein dan
asam nukleat.
• Terdapat tiga bentuk pembuangan senyawa bernitrogen
pada dunia hewan:
– Amonium beracun namun mudah larut dalam air.
Senyawa ini mudah dibuang dari tubuh namun
membutuhkan banyak air.
– Urea memiliki toksisitas yang rendah mudah disimpan
dan di ekskresikan
– Asam urat berbentuk pasta, pembuangannya
membutuhkan sedikit air.
Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
Proteins Nucleic acids

Amino acids Nitrogenous bases

–NH2
Amino groups

Most aquatic animals, Mammals, amphibians, Birds, insects, many


including many fishes sharks, some bony fishes reptiles, land snails

Ammonia Urea
Uric acid Figure 25.8

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Sistem ekskresi memegang peranan penting dalam
keseimbangan tubuh

• Sistem ekskresi
– Membuang
sisa-sia (Inferior

metabolisme vena cava)

Renal artery Kidney


and vein

– Mengatur (Aorta)

cairan dan Ureter

keseimbangan Bladder

Urethra
garam
A. THE EXCRETORY SYSTEM

Figure 25.9A

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


• Terdapat sepasang ginjal pada manusia, tiap
ginjal mengandung jutaan unit fungsional yang
disebut nefron
• Urin meninggalkan ginjal melalui ureter
• Urin untuk sementara ditampung dalam
kantung kemih

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Bowman’s Nephron
capsule
Renal tubule
Renal
medulla cortex
Renal artery
Renal
cortex
Renal vein Collecting
Renal duct
pelvis Renal
medulla
Ureter
To
renal
pelvis

B. THE KIDNEY C. ORIENTATION OF A NEPHRON WITHIN THE KIDNEY

Figure 25.9B, C

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


• Setiap nefron Bowman’s capsule
1 Proximal tubule

terdiri dari tubulus


Glomerulus

Arteriole Capillaries

yang berlekuk dan from renal


artery

berhubungan Arteriole
from glomerulus
3 Distal
tubule
dengan pembuluh
darah
Branch of From
renal vein another
nephron

– Nefron berperan Collecting


menyaring plasma duct
2 Loop of Henle
darah with capillary
network

– Filtrat kemudian
diproses sehinga
dihasilkan urin dalam
jumlah yang rendah D. DETAILED STRUCTURE OF A NEPHRON

Figure 25.9D

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Fungsi kunci dari sistem ekskresi adalah filtrasi,
reabsorbsi, dan ekskresi

• Filtrasi
– Disebabkan oleh adanya tekanan darah.

• Reabsorbsi
– Nefron mengambil senyawa-senyawa di dalam
filtrat yang masih dapat dipergunakan kembali.

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


• Sekresi
– Nefron membuang substansi dan
menambahkannya ke dalam filtrat

• Ketiga proses diatas menghasilkan urin yang


siap disekresikan

Nephron tubule
FILTRATION REABSORPTION EXCRETION
SECRETION
H2O, other small molecules Urine

Capillary

Figure 25.10

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


From blood to filtrate to urine: A closer look

• The proximal tubule reabsorbs


– nutrients
– salts
– water

• Antidiuretic hormone and other hormones


regulate the amount of salt and water the
kidneys excrete

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


• Pengaturan sekresi of H+ dan reabsorbsi ion
bikarbonat membantu dalam proses
pengaturan pH darah
• Sekresi juga meliputi transpor aktif dari obat-
obatan dan senyawa beracun
• Reabsorbsi dari garam dan urea memicu
timbulnya tekanan osmotik yang berperan
dalam proses penyerapan air.

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Proximal tubule Distal tubule
Bowman’s
capsule NaCl H2O Glucose and H2O
HCO3– amino acids NaCl HCO3–
Blood

Some NH H+ K+
3 H+
Filtrate drugs Collecting
H2O and poisons duct
CORTEX
Salts (NaCl, etc.)
MEDULLA
HCO3–
H+ Loop of
Urea Henle NaCl
Glucose
Amino acids NaCl
Some drugs H2O

Reabsorption
Urea
Active transport
NaCl H2O
Passive transport
Secretion
(active transport)

Urine (to renal pelvis)

Figure 25.11

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
BIOLOGY
CONCEPTS & CONNECTIONS
Fourth Edition

Neil A. Campbell • Jane B. Reece • Lawrence G. Mitchell • Martha R. Taylor

CHAPTER 27
Reproduction and Embryonic
Development

Module 27.1

From PowerPoint® Lectures for Biology: Concepts & Connections


Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
• Semua hewan memiliki tiga tahap
perkembangan embrio
– Pembelahan secara mitosis
– Diferensiasi sel
– Pembentukan badan dan strukturnya

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


ASEXUAL AND SEXUAL REPRODUCTION
27.1 Reproduksi seksual dan seksual umum terjadi
pada dunia hewan
• Reproduksi aseksual
– Bertunas
– Pembelahan
– Fragmentasi
– Perkembangan dari telur
yang tidak difertilisasi
Figure 27.1A

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


• Reproduksi seksul
– Pembelahan dari hasil fusi dua sel haploid

Figure 27.1D

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


• Rotifers dapat
“Head”
bereproduksi seksual
dan aseksual Intestine
Ovary

Eggs

• Hermaphroditism
– Satu individu yang
yang memiliki
kelamin jantan dan
betina
Figure 27.1B, C

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


• Keuntungan reproduksi aseksual
– Hanya membutuhkan satu jenis untuk
reproduksi
– Keturunan diproduksi dengan cepat

• Kelemahan reproduksi aseksual


– Sedikit atau tidak ada variasi

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


• Keuntungan reproduksi aseksual
– Peningkatan variasi genetik
– Meningkatkan kemampuan populasi untuk
bertahan terhadap lingkungan yang kurang
menguntungkan

• Kelemahan
– Memerlukan lokasi hewan

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


BIOLOGY
CONCEPTS & CONNECTIONS
Fourth Edition

Neil A. Campbell • Jane B. Reece • Lawrence G. Mitchell • Martha R. Taylor

CHAPTER 27
Reproduction and Embryonic
Development

Modules 27.2 – 27.3

From PowerPoint® Lectures for Biology: Concepts & Connections


Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
Reproduksi Manusia
27.2 Anatomi reproduksi wanita

• Ovari
– Mengandung Ovaries Oviduct

folikel tempat
pertumbuhan
telur Corpus luteum Follicles
Uterus Wall of uterus

– Menghasilkan Endometrium
(lining of uterus)

hormon sek
Cervix
(“neck” of uterus)

Vagina

• Oviducts
– Mengalirkan
Figure 27.2A

telur ke uterus
Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
• Uterus
– Tempat
berkembangny
a zigot
Ovaries Oviduct

• Vagina
– Saluran lahir Corpus luteum Follicles
Uterus Wall of uterus
Endometrium
(lining of uterus)
Cervix
(“neck” of uterus)

Vagina

Figure 27.2A

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


• Ovulasi
– Pelepasan sel telur dari ovarium

Egg
cell

Figure 27.2B

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Oviduct

Ovary

Uterus

Bladder
Rectum
(excretory system)
(digestive system)
Pubic bone

Cervix Urethra
(excretory system)

Shaft
Vagina
Glans Clitoris
Bartholin’s gland Prepuce
Labia minora

Labia majora

Vaginal opening

Figure 27.2C
Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
27.3 Anatomi reproduksi jantan

• Semen
– Sperm, yang dilepaskan selama ejakulasi
– Sekresi kelenjar yang membawa, memberi
nutrisi, dan melindungi sperma

• Testes
– Memproduksi sperma
– Terletak diluar rongga tubuh, di dalam skrotum

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Bladder Seminal
(excretory vesicle
system) (behind
bladder)

Prostate gland

Bulbourethral
gland
Urethra
Erectile tissue
of penis

Scrotum
Vas deferens

Epididymis

Testis Glans of
penis

Figure 27.3B

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Bladder
Seminal vesicle (excretory
Rectum system)
(digestive system)
Pubic bone
Vas deferens
Ejaculatory Erectile tissue
duct of penis

Prostate gland Urethra


Vas deferens
Bulbourethral gland Glans of penis
Epididymis
Testis
Scrotum Prepuce

Figure 27.3A

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


• Hormon androgen menstimulasiproduksi
sperma
– Hormon ini juga menjaga homeostasis melalui
mekanisme feedback negatif yang bekerja
dengan cara menghambat sekresi FSH dan LH

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Stimuli from other
areas in the brain
Hypothalamus

Releasing
hormone

Negative feedback
Anterior
pituitary

FSH LH

Androgen
production

Testis
Sperm
production
Figure 27.3D

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


BIOLOGY
CONCEPTS & CONNECTIONS
Fourth Edition

Neil A. Campbell • Jane B. Reece • Lawrence G. Mitchell • Martha R. Taylor

CHAPTER 27
Reproduction and Embryonic
Development

Modules 27.4 – 27.8

From PowerPoint® Lectures for Biology: Concepts & Connections


Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
27.4 Pembentukan sperma dan ovum terjadi
secara miosis

• Spermatogenesis
– Memproduksi sperma pada pria

• Oogenesis
– Memproduksi ovum pada wanita

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


• Spermatogenesis
– Meningkatkan variasi genetik
– Spermatosit primer diproduksi selama masa
reproduksi dari pria
– Sel diploid membelah secara miosis
menghasilkan 4 sperma fungsional

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Epididymis

Testis Penis
Scrotum

Diploid cell Testis


Differentiation and Seminiferous tubule
onset of MEIOSIS I
Cross section of
seminiferous
PRIMARY SPERMATOCYTE tubule
(in prophase of MEIOSIS I)
MEIOSIS I completed

SECONDARY SPERMATOCYTE
(haploid; double chromatids)
MEIOSIS II

Developing sperm cells


(haploid; single chromatids)
Differentiation

SPERM CELLS Center of


(haploid) seminiferous
tubule

Figure 27.4A

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


• Oogenesis
– Sebagian besar proses terjadi di ovarium
– Oosit primer yang akan dipakai selama masa
reproduksi telah diproduksi saat lahir
– Satu oosit primer matang tiap bulan untuk
menjadi oosit sekunder
– Jika oosit sekunder di fertilisasi, proses miosis
akan komplit dan berkembang menjadi ovum

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Diploid cell In embryo

Differentiation and
onset of MEIOSIS I

PRIMARY OOCYTE,

arrested in prophase Present at birth


of MEIOSIS I

Completion of MEIOSIS I
and onset of MEIOSIS II

SECONDARY OOCYTE,
First
arrested at metaphase
polar body
of MEIOSIS II;
released from ovary

Entry of sperm triggers


completion of MEIOSIS II

OVUM
Second
(haploid) polar body

Figure 27.4B

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


• Development of an ovarian follicle

Degenerating Start: PRIMARY OOCYTE


corpus luteum
within follicle
CORPUS LUTEUM

Growing
follicles

Mature follicle

SECONDARY Ovary
OOCYTE
OVULATION Ruptured follicle Figure 27.4C

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


27.5 Hormones synchronize cyclical changes in the
ovary and uterus

Table 27.5

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(1) CONTROL BY HYPOTHALAMUS Inhibited by combination
of estrogen and
progesterone
Hypothalamus
Stimulated by high
Releasing levels of estrogen
hormone

Anterior pituitary

FSH LH

(2) PITUITARY HORMONES


IN BLOOD LH peak triggers
ovulation and
corpus luteum
formation

LH

FSH

FSH LH

Figure 27.5

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


(3) OVARIAN CYCLE

Growing Corpus Degenerating


Mature Ovulation luteum corpus
follicle follicle luteum
Pre-ovulatory phase Post-ovulatory phase

Estrogen Progesterone
and estrogen
(4) OVARIAN HORMONES
IN BLOOD

Estrogen
Progesterone

Estrogen Progesterone
and estrogen
(5) MENSTRUAL CYCLE

Endometrium

Days Figure 27.5 (continued)


Menstruation
Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
BIOLOGY
CONCEPTS & CONNECTIONS
Fourth Edition

Neil A. Campbell • Jane B. Reece • Lawrence G. Mitchell • Martha R. Taylor

CHAPTER 27
Reproduction and Embryonic
Development

Modules 27.9 – 27.15

From PowerPoint® Lectures for Biology: Concepts & Connections


Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
Prinsip dasar perkembangan embrio
27.9 Fertilisasi menghasilkan zigot dan memicu
perkembangan embrio

• Bentuk sperma manusia terdaptasi sesuai


dengan fungsinya
Middle Neck
piece Head
Plasma membrane

Tail

Mitochondrion
(spiral shape)
Nucleus
Acrosome

Figure 27.9B

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


• Hanya satu sperma
yang akan berhsil
membuahi sel telur

– Fertilisasi adalah
penggabungan
sperma dengan sel
telur untuk
membentuk zigot
yang diploid
Figure 27.9A

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


• Process of 1 The sperm
approaches
the egg
2 The sperm’s

fertilization
acrosomal enzymes
digest the
egg’s jelly 3 Proteins on the
SPERM
coat sperm head bind
to egg receptors
4 The plasma membranes
of sperm and egg fuse
Sperm
head 5 The sperm
nucleus
enters
Nucleus the egg
cytoplasm
Acrosome
Acrosomal
Plasma 6 A
membrane enzymes fertilization
envelope
forms
Receptor protein
molecules
Plasma Sperm
membrane nucleus
Vitelline
layer Cytoplasm Egg
Jelly
nucleus
coat
EGG CELL 7 The nuclei
of sperm
and egg fuse Zygote
nucleus

Figure 27.9C
Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
27.10 Pembelahan menghasilkan sekelompok sel
dari hasil permbelahan zigot

• Pembelahan merupakan salah satu fase utama


dalam perkembangan embrio
– Proses pembelahan yang sangat cepat
– Menghasilkan multiseluler embrio dari zigot

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


• Fase
pembelahan
pada bulu ZYGOTE
babi
2 cells

4 cells

8 cells

Blastocoel

Many cells
(solid ball)

BLASTULA Cross section


Figure 27.10 (hollow ball) of blastula
Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
27.11 Gastrulasi menghasilkan embrio dengan 3
lapisan embrional

• Gastrulasi merupakan fase utama yang ke-2


dari perkembangan embrio
– Menambahkan sel dalam jumlah yang lebih
besar ke embrio
– Menyusun semua sel ke dalam 3 lapisan sel yang
terpisah
– Embrio berubah dari fase blastula ke fase
gastrula

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


• Ketiga lapisan sel tersebut adalah
– Ektoderm
– Endoderm
– Mesoderm

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Animal pole Blastocoel

• Perkembangan 1
gastrula
Vegetal pole BLASTULA
GASTRULATION

Blastopore
forming
Blastopore
forming Blastocoel
shrinking
Archenteron

Archenteron
Ectoderm
Mesoderm

Endoderm
4

Yolk plug
Yolk plug
GASTRULA
Figure 27.11C

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


27.12 Organ mulai terbentuk setelah proses
gastrulasi
• Lapisan embrio mulai berdiferensiasi menjadi
jaringan spesifik dan sistem organ
• Pada chordates
– notochord berkembang dari mesoderm
– Bumbung neural berkembang dari ektoderm

• Bumbung neural berkembang menjadi otak dan


susum tulang belakang

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Neural Neural
plate
fold
Neural Neural
fold plate

Notochord
Ectoderm

Mesoderm

Endoderm
Archenteron

Neural folds

Outer layer
of ectoderm

Neural tube

Figure 27.12A, B

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Neural tube

• Somit merupakan Notochord


gumpalan Somite

mesoderm yang Coelom

akan berkembang
menjadi struktur
segmental Archenteron
(digestive cavity)

Somites Tail bud


• Rongga tubuh
(solemo) juga
berkembang
dari mesoderm Eye

Figure 27.12C

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


Table 27.12

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


BIOLOGY
CONCEPTS & CONNECTIONS
Fourth Edition

Neil A. Campbell • Jane B. Reece • Lawrence G. Mitchell • Martha R. Taylor

CHAPTER 27
Reproduction and Embryonic
Development

Modules 27.16 – 27.19

From PowerPoint® Lectures for Biology: Concepts & Connections


Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
Perkembangan manusia
27.16 Embrio dan plasenta terbentuk selama bulan
pertama kehamilan

• Gestation adalah masa kehamilan


– Dimulai dari fertilisasi sampai kelahiran
– Masa kehamilan manusia 266 hari
(38 weeks or 9 months)
– Masa kehamilan mencit 1 bulan
– Kehamilan gajah 22 bulan

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


• Perkembangan manusia dimulai saat fertilisasi
terjadi di oviduk

Cleavage starts

Fertilization
of ovum

Ovary
Oviduct

Secondary
oocyte
Blastocyst
(implanted)
Ovulation
Endometrium

Uterus

Figure 27.16A

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings


• Fase pembelahan
memproduksi ENDOMETRIUM

blastokista Inner cell mass

– Blastokis
memiliki rongga
yang terisi cairan
– Bagian dalam dari Cavity

sel akan
membentuk bayi
Trophoblast

– Bagian terluar
membentuk Figure 27.16B

trophoblast
Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
• Trophoblast mensekresikan enzim yang
memungkinkan terjadinya implantasi

ENDOMETRIUM Blood vessel


(maternal)

Future embryo

Multiplying cells
of trophoblast
Future
yolk sac

Trophoblast

UTERINE CAVITY

Figure 27.16C

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• Gastrulasi terjadi dan organ terbentuk dari
ectoderm, endoderm, and mesoderm

Amniotic
cavity Amnion

Mesoderm
cells Chorion

Yolk sac

Figure 27.16D

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• Selain itu, empat membran ekstra embrionik
terbentuk
– Amnion
– Chorion Chorion Chorionic villi

Amnion EMBRYO:

– Yolk sac Allantois Ectoderm


Mesoderm
– Allantois Endoderm
Yolk sac

Figure 27.16E

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• Embrio terbenam pada rongga amnion yang
berisi cairan, sementara korion dan lapisan
mesoderm membentuk plasenta
Placenta Mother’s blood
vessels

• Korio vili dari Allantois

Yolk sac
plasenta Amniotic
cavity

menyerap
Amnion
Embryo

nutrisi dan
oksigen dari Chorion

peredaran Chorionic
darah ibu villi

Figure 27.16F
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• Plasenta juga memungkinkan The placenta
allows for a variety of substances to pass from
mother to fetus
– Protective antibodies
– German measles virus
– HIV
– Drugs (prescription and nonprescription)
– Alcohol
– Chemicals in tobacco smoke

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27.17 Perkembangan manusia dari fertilisasi
samapai kelahiran dibagi menjadi 3
trisemester
• Trisemester pertama

Figure 27.17A, B

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• Second trimester
– Increase in size of fetus
– General refinement of human features

Figure 27.17C, D

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• Third trimester
– Growth and
preparation for
birth

Figure 27.17E

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27.18 Proses kelahiran diinduksi oleh hormon dan
terjadi dalam 3 tahapan

• Prubahan hoa kelahiran


– Kalahiran dikontrol melalui mekanisme umpan
balik positif
– Pelepasan estrogen dari ovarium meningkatkan
sensitifitas uterus terhadap oksitosin

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• Oksitosin merupakan stimulus yang kuat bagi
otot polos di uterus
– Oxytocin juga menginduksi plasenta
memproduksi prostaglandin yang memicu
uterus berkontraksi lebih kuat
• Kontraksi uterus memicu pelepasan oksitosin
dan prostaglandin lebih besar

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ESTROGEN OXYTOCIN

from From fetus


ovaries and pituitary

Induces oxytocin

Positive feedback
receptors on uterus

Stimulates uterus
to contract

Stimulates
placenta to make

PROSTAGLANDINS

Stimulates more
contractions
of uterus

Figure 27.18A

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