Beruflich Dokumente
Kultur Dokumente
CURRICULUM
Stage 3 Semester 1
BIOCHEMISTRY PRACTICAL
2014/2015
School of Biomolecular and Biomedical Science &
School of Medicine and Medical Science,
University College Dublin,
Belfield,
Dublin 4.
TITLE
: ANALYSIS OF PLASMA
LIPOPROTEINS
Title:
Analysis of Plasma Lipoproteins
Aim:
1. To carry out a biochemical analysis of the cholesterol and triglyceride profile of
the serum prepared from three donor volunteers and
2. To make a clinical assessment of the results with respect to risk of development of
cardiovascular disease.
Methodology:
Determination of total cholesterol in plasma or serum
Solution 2
10 l plasma
1 ml Reagent solution.
3. Each solution was mixed and incubated for 20 minutes at room temperature.
4. The absorbance of sample against blank (within 10 minutes) at 500nm was read
5. The concentration of cholesterol in the plasma was calculated in unit mmol/l.
c= 14.3 x A 500nm sample
Solution 1
0.1ml
1ml
Solution 2
0.1ml
1ml
5. Each solution was mixed and incubated for 20 min at room temperature.
6. The absorbance of sample was measured against blank at 500nm within 10 min.
7. The concentration of HDL- cholesterol was measured in mmol/l
c= 4.65 x A500nm sample
3. Each solution is prepared as below. The solutions are then mixed and left to stand
for 20 minutes at room temperature.
Chromogen reagent
Standard
Plasma
Blank
1 ml
-
Standard
1 ml
10 l
-
Sample
1 ml
10 l
6. The level was used to determine the relationships using equation below:
d)
e)
VLDL cholesterol (mmol/l) = [Total cholesterol] [HDL cholesterol] [LDL cholesterol]
2. The results for 3 donors serum sample relative to the value in Table 3 below were
compared. The clinical assessment of the data with respect to the donors risk of
development of cardiovascular disease were made.
Table 3: Normal, Borderline and High Risk Distribution for Plasma Lipoprotein
Cholesterol and Plasma Triglyceride
Category
Normal
Borderline
High Risk
Total Plasma
Cholesterol
mmol L-1
5.1<
5.1 to 6.2
>6.2
Plasma
Triglyceride
mmol L-1
1.68<
1.69 to 2.23
2.24 to 4.4
HDL
Males
LDL
Female
>1.28
1.27 to 1.03
1.02<
>1.53
1.52 to 1.15
1.14<
2.5 to 3.3
3.4 to 4.1
>4.2
3. A middle aged man (47 years) presents to your medical clinic with high
cholesterol using the pin-prick test, his total cholesterol 8.5 mmol L-1. His
triglyceride level was
subsequently determined to be 7.0 mmolL-1 and his
glucose determined as 10.5 mmolL-1.
a) Suggest ways in which you would advise this patient.
Treatments are advised since the man has high risk distributions for plasma
lipoprotein, cholesterol, and plasma triglyceride and glucose level. Medicine such
as statin and insulin should be given. Besides, the patient should include Omega-3
fatty acids in his diet to lower the triglycerides level. Soluble fiber can lower the
absorption of cholesterol in the intestine, thus increasing patients fiber intake can
be another option. Moreover, patients should be advised to do more exercise. A
diet low in fat, salt and sugar and high in fiber and with plenty of fruit and
vegetables should be taken to reduce blood glucose level. Exercise can raise HDL
and lowering triglycerides at the same time. Other advices such as quit smoking if
your patient smoke and watch the alcohol should be given.
b) Would you recommend a full biochemical analysis of the profile of cholesterol
i.e as carried out in your practical? If yes explain?
Yes, the patient has high risk distribution for cholesterol with the value of
8.5mmol L-1 while the borderline is 6.2mmol l-1. Thus, a full biochemical
analysis should be carried out to increase the accuracy of the measurement. This
is because pin-prick test only measure total cholesterol. A full understanding of
your cholesterol profile requires measurements of HDL, LDL, and triglycerides as
well. Second, the results need combination with other risk factors such as family
history, nutritional habits, age, and gender to fully understand the risk for
cardiovascular disease.Treatment can be carry out before the condition get worst.
c) Suggest some initial queries you would make to the individual with respect to his
lifestyle.
I would need to enquire more about the family history of premature heart disease,
medical history such as pre-existing heart disease or already had a heart attack,
hypertension, diabetes mellitus. Enquiry included smoking and drinking alcohol
habit should be included as well.
Cholestyramine These compounds are nonabsorbable resins that bind bile acids
or
colestipol which are then not reabsorbed by the liver but excreted. The
(resins)
drop in hepatic reabsorption of bile acids releases a feedback
inhibitory mechanism that had been inhibiting bile acid
synthesis. As a result, a greater amount of cholesterol is
converted to bile acids to maintain a steady level in circulation.
Additionally, the synthesis of LDL receptors increases to allow
increased cholesterol uptake for bile acid synthesis, and the
overall effect is a reduction in plasma cholesterol.
Ezetimibe
Discussion
Conclusion