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The Natural Products Journal, 2015, 5, 115-123 115

Sauropus androgynus Leaves for Health Benefits: Hype and the Science

Hock Eng Khooa,b, Azrina Azlana,b,* and Amin Ismaila,b


a
Department of Nutrition and Dietetics, Faculty of Medicine and Health Sciences, Universiti Putra
Malaysia, UPM Serdang, 43400 Selangor, Malaysia; bResearch Centre of Excellence, Nutrition and
Non-Communicable Diseases, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia,
43400 UPM Serdang, Selangor, Malaysia

Abstract: Sauropus androgynus (SA) is a medicinal plant with high antioxidant potential. The leaves
of this plant have been traditionally used to treat certain diseases, for weight loss, and as vegetable
dishes. SA leaves contain an adequate amount of macronutrients and having most of the
micronutrients. The micronutrients are phenolic compounds, carotenoids, antioxidant vitamins, and
minerals. SA leaves also contain most of the essential minerals, including sodium, potassium, calcium, phosphorus, iron,
magnesium, copper, zinc, manganese, and cobalt. Fresh leaves of SA typically consist of 70%-90% moisture, 3%-8%
protein, 1%-4% fat, 1%-2% fiber, and about 2% ash. The other percentage of the leaves is carbohydrate. In this review,
the types and amounts of phenolic compounds, carotenoids, antioxidant vitamins, and minerals are presented.
Antinutrients and heavy metals detected in SA leaves are also revealed. These compounds could have adverse health
effects, such as heavy metal toxicity and induce lung injury. Bronchiolitis obliterans and obstructive ventilatory
impairment of the patients are known to be caused by ingestion of uncooked or fresh SA leaves. SA leaves are the staple
food in some of the developing nations that provide essential nutrients to the poor people. It also helps to maintain good
health of these people. However, fresh consumption and over-consumption of SA leaves are not advisable. It may cause
toxicity or lung injury. The antioxidative components of SA leaves have scientifically shown a vast health benefit to the
human being, from test tubes to in vivo studies. However, extra precaution should be taken for minimizing the adverse
health effect of intake of fresh SA leaves.
Keywords: Antioxidant, health benefit, intoxicant, leaves, nutrient, Sauropus androgynus.

INTRODUCTION Traditionally, the leaves of SA are commonly used for


treating genitor-urinary diseases, cardiovascular diseases and
Sauropus androgynus (SA), also called star gooseberry,
some other diseases [3]. In Indonesia, SA leaves have been
is a tropical shrub grown as a leafy vegetable. It is from
used as one of the ingredients for jamu. Jamu is traditionally
Euphorbiaceae family. In Malaysia, it is named as cekor
used to restore uterus and abdomen to the original size after
manis or katuk. The Indian, Indonesian, and Thai names of
SA are Chakrmani, Katu, and Phak Wan Ban, respectively. giving birth and for relieving fatigue [4]. SA leaves have also
The plant is known to be introduced from Malaya to India been used to reduce body weight and to improve vision
[1]. The tree of SA can grow up to 3 m in height, and the according to the studies performed in Taiwan and Southeast
leaves are oblong in shape. The leaves are typically 2-6 cm Asia [5]. Besides, the leaves of SA have been traditionally
long and 1-3 cm wide, the top and bottom of the leaves are used in India for good vision and skin problems [6]. Until
dark green and lighter green, respectively. now, there is no documentation of clinical trial on the
prevention and treatment of these diseases using SA leaves.
SA leaves are commonly known as sweet leaves due to Conversely, eating the leaves in a large amount can cause
the sweet taste of the leaves after cooking. The leaves are a nausea, dizziness, vomiting, diplopia, sedation, weakness,
typical Indian vegetable dish. The physicochemical and uncontrolled eye movements [7]. On the other hand, the
properties of SA leaves have been reported by Christi [2]. protective effect of SA leaves could be due to the
The leaves contained 4.28% total ash, 0.81% acid insoluble antioxidative compounds in the leaves [2].
ash, 1.24% water insoluble ash, and 3.42% sulphated ash; the
solvent extractable yields were 24.1% for methanol, 9.67% Green leafy vegetables contain a high amount of
for chloroform, 17.4% for benzene, 13.3% for petroleum carotenoids, vitamins, and minerals [7]. Besides these
ether, and 20.6% for water. Besides that, the swelling factor nutrients, other bioactives are mainly lignan and
of the leaf powder was 9 ml. megastigmane glycosides [8]. Carotenoid and polyphenol are
also the typical antioxidants in green leafy vegetables. Beta-
carotene is the major carotenoid in plant. However, some of
*Address correspondence to this author at the Department of Nutrition and
the green leafy vegetables have a high amount of
Dietetics, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, xanthophylls, such as lutein and zeaxanthin. The leaves of
UPM Serdang, 43400 Selangor, Malaysia; Tel/Fax: +603-8947-2466; SA contain significantly higher total flavonoid content than
E-mail: azrinaaz@upm.edu.my the other studied leafy vegetables except the leaves of

2210-3163/15 $58.00+.00 © 2015 Bentham Science Publishers


116 The Natural Products Journal, 2015, Vol. 5, No. 2 Khoo et al.

Calamus scipronum (Semambu leaves) [9]. Among the NUTRITIONAL COMPOSITIONS


flavonoids determined in the study, quercetin and
kaempferol were the major flavonoids detected in SA leaves. Macronutrients
SA leaves possess a high total phenolic content and The leaf of SA is a nutritious food. Nutrients of the leaf
antioxidant activities. The total phenolic content of SA compliment with other food for an individual to obtain
leaves of Indonesian origin was not significantly lower than enough macronutrients for survival. The proximate
the total phenolic content of the leaves of Cosmos caudatus compositions or macronutrient contents of SA leaves are
(Ulam Raja leaves) [10]. Based on the electron transfer depicted in Table 1. SA leaves have moisture content
reaction assays, SA leaves contained higher antioxidant ranging between 69.9% and 89.9%, and the protein contents
activities than many other leafy vegetables of Indonesian of both dry and fresh samples of SA are in the range between
origin. Due to the beneficial effect of SA leaves in reducing 4.2% and 29.15%. Some of the SA leaf samples have high
body weight and possessing antinematodal activity, the fiber content, and the carbohydrate content of SA leaves
leaves should have containing bioactive antioxidants, such as have not been reported by some of the previous studies.
carotenoids, flavonoids, and other phytochemicals. These
phytochemicals can reduce oxidative stress, thus reduce the Vitamins and Minerals
risk of some chronic diseases.
Vitamin and mineral contents of SA leaves have been
Although no scientific evidence has proven the protective determined previously using chromatographic and
effect of SA leaves against certain chronic diseases, the spectrophotometric methods. The vitamin and mineral
search for a prevention of these diseases using SA leaves is contents of SA leaves are depicted in Tables 2 and 3,
still ongoing. Based on the scientific evidences, the possible respectively. The major vitamins for the leaves are vitamins
health benefits of SA leaves are discussed in this review. A and C. Vitamin A of SA leaves is probably due to the pro-

Table 1. Nutritional composition of Sauropus androgynus (SA) leaves.

Composition India India India* Thailand* Thailand* Indonesia Indonesia* Vietnam Malaysia
[7] [11] [6] [12] [14] [13] [10, 15] [16] [17]

Energy (kcal) ˗ 28.0 ˗ 40.4 317 401.4 ˗ ˗ 100.5

Moisture (%) 69.9 88.0 85.4 88.5 89.9 - 82.9g 86.9 79.4

Protein (%) 7.4 3.4 5.3 4.2 15.8 29.2 8.31h ˗ 7.6

Carbohydrate (%) ˗ 0.5 ˗ 3.9 54.5 - ˗ ˗ 6.9

Fat (%) 1.1 1.4 0.6 0.9 4.0 4.6 ˗ ˗ 1.8

Fiber (%) 1.8 1.7 1.8 1.2 36.0 8.2 ˗ ˗ 1.9

Ash (%) ˗ - 5.3 1.4 12.9 12.1 - 1.4 2.0


Footnote: * indicates the data have been reported in the review article by Petrus [18]. For the samples obtained from Thailand [14] and Indonesia [13]; the compositions are
expressed as % dry weight (DW) excluding the moisture content.

Table 2. Vitamins content of Sauropus androgynus leaves.

Place of Origin Vitamin A Thiamine Riboflavin Vitamin C


(β-carotene Equivalent) (Vitamin B1) (Vitamin B2) (Ascorbic Acid)

India [7] 5.6 ± 0.2 0.5 ± 0.03 0.21 ± 0.01 244 ± 15

India [20] - - - 22.0


*
India [6] 19.4 ± 0.6 - - 314.3 ± 1.8

Thailand* [14] - - - 56.1

Thailand [21] 4.4 ± 0.1 - - 114.9 ± 0.6


*
Indonesia [15] - - - 190.83 ± 0.82

Vietnam [16] 5.3 - - -

China [22] - - - 31.25


Footnote: * indicates the data have been reported in the review article by Petrus [18]. Values are expressed as mg/100 g of the leaves; fresh weigh (FW) basis [7]; FW basis [20]; FW
basis-µg/100 ml [6]; DW basis-89.9% moisture [14]; FW basis [21]; FW basis [15]; FW basis [16]; FW basis [22].
Health Benefits of Sauropus androgynus The Natural Products Journal, 2015, Vol. 5, No. 2 117

Table 3. Minerals content of Sauropus androgynus (SA) leaves.

Composition India India* India* Thailand* Thailand* Indonesia Vietnam


[7] [20] [6] [12] [14] [13] [16]

Na - - 306.3 ± 52.8 396.0 - - -

K - - 45.7 ± 1.5 - - - -

Ca 771 ± 11 313.0 84.4 ± 8.1 70.5 118.8 249.9 158

P 543 ± 18 - 61.2 ± 3.5 128.2 - 300 -

Fe 8.8 ± 0.3 10.09 212.5 ± 20.8 0.9 13.5 36.4 1.6

Mg - - 664.9 ± 38.1 - - 1004.3 -

Cu

Zn - - 15.9 ± 6.6 0.9 - 20.2 1.0

Mn - - 25.6 ± 5.8 - - - -

Co - - 1.6 ± 0.1 - - - -

Footnote: * indicates the data have been reported in the review article by Petrus [18]. Values are expressed as mg/100 g of the leaves; FW basis [7]; FW basis [20]; DW basis-85.4%
moisture [6]; FW basis [12]; DW basis-89.9% moisture [14]; FW basis [13]; FW basis [16].

vitamin activity of carotenoid, such as β -carotene. The SA The minerals attribute to dietary intake from the leaves of
plant, including the leaf, has vitamin C content of 22-244 SA were zinc (4.3 mg/kg FW) and iron (14.8 mg/kg FW),
mg/100 g fresh weight (FW). The wide range of vitamin C which based on a cross-sectional study among the female
in SA plant (including leaves) could be due to several populations of two farming villages in the Red River Delta,
reasons. The typical reasons are different parts of SA Vietnam [19]. The study showed that consumption of
plant and methods of analysis used. Besides these vitamins, SA leaves helped to improve the nutritional status of the
vitamins B1 and B2 contents quantified in the SA leaves are poor people in Vietnam, especially when consuming a
0.5 and 0.21 mg/100 g FW, respectively. The amounts of mixture of fresh leaves of SA, amaranth, mustard green, and
these B vitamins are considered higher than many other leafy spinach.
vegetables. The SA leaves also contain α-tocopherol, which
is 42.68 ± 0.12 mg/100 g edible portion [11]. BIOACTIVE ANTIOXIDANTS
Essential minerals, as the most important elements in the The total phenolic content (TPC) of SA leaves has been
human body, are also abundantly found in SA leaves. As well determined and reported in a review article by Petrus
shown in Table 3, the minerals detected in SA leaves are [18]. Based on the previous studies, TPCs of SA leaves were
sodium (Na), potassium (K), calcium (Ca), phosphorus (P), 11.5 mg GAE/g DW [14], 11.51 ± 2.9 mg GAE/g DW [5],
iron (Fe), magnesium (Mg), zinc (Zn), manganese (Mn), and 20 mg GAE/g DW [23], 19 mg GAE/g FW [24], 1.49 mg
cobalt (Co). The leaves of SA also contain vanadium (Va), GAE/g FW [10], and 1.38 mg GAE/g FW [15]. Besides,
selenium (Se), and chromium (Cr) [18]. Some of these TPC of the methanolic extract of SA leaves from India was
minerals from the leaves can be toxic to the human body if 9.82% (w/w) [25]. It shows that the leaves of SA have high
taken in high doses. A high Ca content (771 mg/100 g FW) total phenolics. However, the total flavonoid content in the
was determined for the SA leaves from India as compared to leaves of C. scipronum was 2.6 times higher than the total
the other countries (Table 3). Besides, Indonesian SA leaves flavonoid content of the leaves of SA. Morever, the TPC of
contained a higher amount of Mg (1004.3 mg/100 g FW) SA leaves from Thailand was 48.42 ± 2.13 mg GAE/100 g
compared with the Mg content of 664.9 mg/100 g dry weight FW [12]. The amounts of total flavonoids and potential
(DW) that determined by the Indian scientist. The SA plant flavonoids are shown in Table 4. Total flavonoid content of
from Indonesia has about 1% of Mg from the edible portion. SA leaves has been determined as 10.4 mg rutin equivalent
The extremely high Mg content in SA plant could be due (RuE)/g DW [14] and 15.3 mg RuE/g FW [24]. The total
to the soil contaminated with magnesium or sample flavonoids reported by Miean and Mohamed [9] (78.5 mg
contamination during sample preparation and analysis. /100 g DW) and by Andarwulan et al. [10, 15] (143 mg/100
In nature, a great variation in minerals content is found g FW) are the total amounts of individual flavonoids
for SA planted in different geographical locations. Soil determined. Besides, total anthocyanin content of SA leaves
contamination and other human activities could contribute to has been reported as 82.8 ± 1.1 mg cyanidin-3-glucoside/100
the greater variation in the mineral composition of SA g DW [6] or 1.53 mg/100 g FW [15].
leaves. However, these essential minerals are needed for the Carotenoids have been detected in SA leaves. The hexane
human body through consumption of the edible portion of extract of SA leaves contained 1.63 ± 0.02 mg/100 g FW of
the plant or leaves. β-carotene, and the total carotenoid content was 5.15 ± 0.07
118 The Natural Products Journal, 2015, Vol. 5, No. 2 Khoo et al.

Table 4. Flavonoids content in the leaves of Sauropus quercetin, isorhamnetin, luteolin, and apigenin were below
androgynus. the detection limit [32].
Another study revealed that the aqueous extracts of SA
Flavonoids Malaysia Indonesia leaves were tested positive for triterpenoids using Salkowski
[9] [10, 15] test [33]. The volatile components of the essential oil from
SA leaves have been determined by Lin et al. [34]. The
Apigenin ND <0.03 results showed that the major components of the essential oil
Kaempferol 32.4 ± 0.01 138.0 ± 5.8
were carvacrol methyl ether, thymol, and butylated
hydroxytoluene. Other phytochemicals detected in SA leaves
Luteolin ND <0.006 using GCMS were 1,14-tetradecanediol, 1-octadecyne,
1-hexadecyne, decanoic acid, ethyl ester, phytol, pyrene,
Myricetin ND <0.00002
napthalenone, azulene, and squalene [35].
Quercetin 46.1 ± 0.01 4.5 ± 0.22
POTENTIAL HEALTH BENEFITS
Total flavonoids 78.5 143.0 ± 6.0
Wild vegetables are rich in micronutrients and
Footnote: The results are expressed as mg/100 g DW [9] and mg/100 g FW (82.9%
moisture) [10, 15]. ND: not detected (below limit of detection).
phytochemicals. These wild vegetables contain potent
antioxidants. As shown in Table 4, previous literature
reported that the leaves of SA have a high level of bioactive
mg β -carotene equivalent/100 g FW [15]. The leaves also antioxidants. An increased consumption of wild vegetables
have all-trans-α- and β-carotene contents of 1.34 and 10.01 such as SA leaves, significantly contributed to the high
mg/100 g FW, respectively [26]. Also, the neoxanthin and overall micronutrient intakes among the rural women in
violaxanthin contents of SA leaves were 9.33 ± 0.45 and Vietnam [36]. Among the phytochemicals, polyphenols are
11.76 ± 1.51 mg/100 g DW, respectively [27]. Besides the well-known bioactives in prevention and treatment of
carotene, the leaves of SA contained 19.5 ± 0.8 mg lutein various diseases. Besides phenolic compounds, guanosine is
and 8.5 ± 0.7 mg zeaxanthin in 100 g FW [28]. The total a potential bioactive in SA leaves that displayed antioxidant
carotene content of SA leaves was 5.6 ± 0.22 mg/100 g fresh activity and protective effect against oxidative damage [37].
leaves. Some of the data have been revealed by Petrus [18]
in a review article. Other than major bioactives, tannic acid Antioxidative Effects
was not detected in the leaves of SA [16]. Conversely, Singh
et al. [6] reported that 88.7 ± 1.1 mg tannin (tannic acid Total antioxidant capacity (TAC) of methanolic extract
equivalent) was detected in 100 g fresh leaves of SA, and the of SA leaves has been determined and expressed as ascorbic
leaves also have chlorophyll content of 45.6 ± 0.7 µg/100 ml acid equivalent. The TAC of SA leaves obtained from India
FW. Besides, hexamositol phosphate (284.0 mmol/100 g was significantly higher than the TAC of the leaves of
FW) was also detected in SA leaves obtained from Vietnam. Trigonella foenum-graecum, Centella asiatica, and Pisonia
alba at extract concentrations of higher than 100 µg/ml [24].
The shoot of SA that containing total flavonoids has been It could be due to the leaves contained a high amount (>200
analyzed using NMR. The result showed that four lignan mg/100 g FW) of ascorbic acid (Table 2). Besides that, the
glycosides, a megastigmane glucoside, guanosine, and antioxidant capacity of Thai’s SA leaves was 17.62 ± 1.93
corchoionoside were identified in the aerial part of SA mg vitamin C equivalent/100 g FW [12]. Similarly, the
[8]. The lignan glycosides were (−)-isolariciresinol results obtained from DPPH scavenging assay showed the
3α-O-β-apiofuranosyl-(1→2)-O-β-glucopyranoside, (+)- highest scavenging for the methanolic extract of SA leaves,
isolariciresinol 3α-O-β-glucopyranoside, (−)-isolariciresinol but not for ABTS and lipid peroxidation assays. The high
3α-O-β-glucopyranoside, and (+)-syringaresinol di-O-β- scavenging activity of SA leaf extract could be due to the
glucopyranoside; the megastigmane was sauroposide. highest levels of total flavonoids and total phenolics
Besides lignan, bioactive flavonoids are also found in the determined among the methanolic extracts of four Indian
leaves of SA. A previous study reported that 3-O-β-D- leafy vegetables. Besides, the methanolic extract of SA
glucosyl-(1→6)-β-D-glucosyl-kaempferol was isolated from leaves has TAC of 85.6 ± 1.02%, where the EC50 value of
the SA plant [29]. TAC was 201.1 µg rutin equivalent/100 g DW [6].
Although no previous study determines the antioxidant Alternatively, antioxidant activities of SA leaves as
activities of these lignan glycosides, lignan glycosides assessed using DPPH and FRAP assays were 130 and 190
isolated from the methanolic extract of Saraca asoca bark µM Trolox equivalent/g DW, respectively, whereas the
have moderate to high antioxidant activities that based on cupric ion chelating activity of the leaves was 79% of cupric
EC50 values of DPPH radical scavenging assay [30]. Based ions chelated [23]. The antioxidant activities of the leaves
on the reported EC50 values, some of the identified lignan were also significantly higher than many other plants
glycosides have antioxidant activity comparable with studied. The high antioxidant activity of SA leaves is known
flavonoids. Besides, six bioactives have also been identified to correlate strongly with TPC, where the DPPH and FRAP
in the aerial part of SA [31]. These bioactives were three assays are based on the electron transfer reaction pathway.
nucleosides, two flavonol diosides, and one flavonol trioside, Conversely, the high antioxidant activities of SA leaf extract
where kaempferol was the major flavonoid in the leaves of could be due to the present of protein components in the
SA. The shoot of SA has 53.8 mg/100 g kaempferol, but extracts, especially aqueous extracts of SA leaves [38]. The
Health Benefits of Sauropus androgynus The Natural Products Journal, 2015, Vol. 5, No. 2 119

antioxidant activity of SA leaves also has been reported as have confirmed lung distress self-reported that they
EC50 of 1.43 µg/ml that based on DPPH radical scavenging consumed SA leaves (juice, extract, or cooked dishes) for
assay [14]. weight loss. The respiratory distress could probably due to
the ingestion of fresh SA leaves.
As assessed using several antioxidant methods, the
methanolic extract of SA leaves has moderate antioxidant Alkaloids, glycosides, and saponin have been detected in
capacities compared with the other medicinal plants in India fresh leaves of most plants. These compounds are somehow
[25]. These antioxidant methods used were ABTS, DPPH, toxic [43]. Although papaverine is one of the main bioactives
lipid peroxidation, H2O2, p-NDA, and nitric oxide assays, in SA leaves, some researchers hypothesized that it can
where the methanolic extracts have EC50 values (µg/ml) of cause bronchiolitis. However, an animal study in Taiwan
12.58, 341.00, 228.75, 370.00, >1000, and >700, proven that ingestion of SA leaves and papaverine do not
respectively. The result also showed that the total antioxidant cause bronchiolitis [44]. In fact, papaverine is an
capacity of SA leaf extract that analyzed using ammonium antispasmodic drug. For that reason, consumption of fresh
molybdate method was 2.41 µM ascorbic acid equivalent/g SA leaves or freshly blended juice of SA leaves is not
extract. Besides, the DPPH radical scavenging activity, recommended for weight loss. Cooking or blanching of SA
reducing power, and metal chelating capacity of SA leaf leaves for consumption as vegetable dishes will somehow
extracts have been determined previously [39]. The SA work better.
leaves were extracted using four types of extraction solvents,
such as petroleum benzene, chloroform, methanol, and Antimicrobial
water. Among the extracts, petroleum benzene has the lowest SA leaves can inhibit the growth of both gram positive
EC50 value (36.25 µg/ml) based on DPPH assay. As and gram negative bacteria. Paul and Anto [45] reported that
compared with water extract of SA leaves, the petroleum the ethanolic extract of SA leaves showed higher inhibitory
benzene extract has 8.5 times lower EC50 value than the effects against Klebsiella pneumonia (gram negative) and
water extract. The petroleum benzene extract of SA leaves Staphylococcus aureus (gram positive) than the aqueous
also has the highest reducing power determined using extract. Besides the inhibitory effects of these bacteria, the
ferricyanide method (1.53 unit of absorbance reading methanolic extract of SA leaves has the highest inhibitory
measured at 700 nm) compared with the lowest absorbance effect against Pseudomonas aeruginosa, S. aureus, Proteus
reading at 0.23 unit for chloroform extract. Besides, the vulgaris, and Bacillus subtilis compared with the methanolic
chelating capacity of ferrous ion (70.7%) for the chloroform extracts of SA stems and roots, except for Eschelicia coli
extract of SA leaves was the highest; however the water [34].
extract of SA leaves has the lowest capacity (48.1%).
Conversely, the aqueous extract of SA leaves has weaker
The results obtained from SA leaf extract were also microbial inhibition than the methanolic extract. The
compared with the other vegetables (curry leaves, celeries, methanol, ethanol, and aqueous extracts of SA were also
sweet potato leaves, winged beans, and garlic chives). tested for antimicrobial activities. Based on the results
Moreover, the EC50 values (95, 135, and 63 µg/ml) of SA leaf obtained from agar diffusion assays, the methanolic extract
extract for ferricyanide reducing power, DPPH, and hydrogen has higher inhibition activity than the aqueous extract of SA
peroxide scavenging assays, respectively, were higher than leaves against six bacterial strains (gram positive and gram
the EC50 values of typical antioxidants, ascorbic acid, and negative bacteria) [46]. However, the inhibition zones of all
epicatechin [2]. Also, the antiradical activity (1/EC50) of SA the extracts were lesser than the standard streptomycin used.
leaves was 0.7 [40]. The 1/EC50 value is higher than many The results also showed that the SA leaf extracts have 41%
other Thai plants. Based on all the reported data, therefore, to 79% of inhibition in relation to streptomycin.
SA leaves are considered as the vegetable with moderately
high antioxidant activities. Anti-inflammatory and Wound Healing

Weight Loss SA leaves possess an anti-inflammatory effect. The


extracts of SA leaves at concentrations of 200 and 400
A flavonoid isolated from SA plant has been shown to mg/kg BW have shown significant reduction (>50%) in the
prevent weight gain in laboratory rats fed with a high-fat carrageenan-induced edema of rat paw in 1 hour compared
diet. The rats supplemented with 60 mg/kg body weight with the drug (papaverine) used [47]. Christi [2] also
(BW) of the flavonoid [3-O-β-D-glucosyl-(1→6)-β-D- reported a significant reduction in edema volumes for the
glucosyl-kaempferol] isolated from SA plant significantly rats fed with 250 mg SA extracts or 1 ml of juice per kg BW
reduced food intake by 15%, and significantly reduced serum compared with the control (0.75% carboxymethyl cellulose).
free triglyceride level without obvious histopathological Addition of lipopolysaccharide to macrophages resulted in a
changes [29]. reduction in the levels of selected inflammatory markers,
Previously, the fresh leaves of SA or juice from the such as cyclooxygenase-2 and its intermediate products
leaves have been used by young and middle-aged women for (prostaglandin E2 and nitric oxide) in a dose-dependent
the perceived weight loss effect. On the contrary, there are manner (20-200 µg/ml) [48].
cases reported in some countries in Asia regarding the Lipopolysaccharide is known to induce oxidative stress
adverse effect of consuming SA leaves [41]. The cases were and increase production of these inflammatory markers in
related to “bronchiolitis interstitial pneumonitis”. Based on a RAW 264.7 cells [49]. Significant reductions in the
study reported by Hung et al. [42], ten healthy women who inflammatory markers show the effectiveness of SA leaf
120 The Natural Products Journal, 2015, Vol. 5, No. 2 Khoo et al.

extract in reducing oxidative stress, thus exhibit the anti- sperm abnormality in mice. Prolong intake of SA leaves
inflammatory effect. Besides, the extract also suppressed damaged the organs of the experimental mice, such as liver,
the gene of cytokine-inducible nitric oxide synthase, where kidney, spleen, heart, lung, and testis; whereas increase dose
it is highly expressed in the lipopolysaccharide-induced of SA leaves could worsen the damage to these organs.
macrophages. Therefore, a long-term consumption of SA leaves is not
advisable because the toxic glycosides from the leaves could
Wound healing effect of SA leaves has been determined
be accumulated in the organs.
by Bhaskar and Ramesh [50]. The authors reported that the
SA leaf extract significantly promoted wound healing On the other hand, consumption of SA leaves could
activity in both male and female rat models. The results benefit lactating women. A study reported that lactating
showed that 5% SA extract was significantly augmented mice supplemented with SA leaf extracts have 2 to 26-fold
wound contraction, re-epithelialized, and increased wound increased expression of prolactin and oxytocin genes in the
breaking strength by applying topically once a day onto the pituitary glands of the mice [58]. It shows that SA leaf
wound. Besides, a histological observation also showed extracts helped to increase the milk production. In a human-
abundant collagenation, fibroblast, and lesser macrophages based study, the leaf extract of SA has been proven to
in the wound tissue of the Wistar rats treated with SA extract increase production of mother’s breast milk. Besides, a study
compared with positive and negative controls. In addition, in Indonesia reported that SA leaf extract has increased
the SA extract has been studied for its anticonvulsant activity breast milk production of lactating mothers up to 50.7%
[51]. compared to placebo [59]. Another similar study proved the
benefit of consuming SA leaves for increasing production of
Other Health Benefits human breast-milk [60]. Moreover, increased consumption
of SA leaves has significantly increased the level of vitamin
Although no previous literature has reported the potential
A in the breast milk of breastfed mothers in a few districts of
cardioprotective effect of SA leaves using in vivo model, a Indonesia [61]. In addition, milk production in mammals
study has demonstrated that fermented SA leaves were
resulting from the consumption of SA leaves has also been
effectively reduced 19.32% cholesterol content in chicken
determined using several animal models.
meat compared to control (ration without addition of
fermented SA leaves) [52]. The experimental chicken were Therefore, the benefits of consuming SA leaves are
fed with fermented SA leaves for eight weeks before related to the bioactive compounds in the leaves, including
slaughtered. The study hypothesized that the cholesterol- carotenoids and phenolic compounds. The main bioactive in
reducing effect in the chicken was mainly contributed by the SA leaf extract was papaverine, where a high concentration
β-carotene content in SA leaves. The effect could be due to (0.38 ± 0.04 µg/ml) of the compound has been determined in
the inhibition of enzyme HMG-CoA reductase activity by β- the extracts.
carotene in the leaves.
SAFETY ISSUES
Consumption of average cumulative dosage of SA leaves
(2.67 ± 1.89 kg, range 0.4-8.0 kg) was shown to significantly In general, the leaves of SA are not toxic to the human
lower Tiffeneau-Pinelli index (FEV1/FVC ratio) of the body if consumed moderately. A study showed that the
patients with respiratory symptoms than the patients without medium lethal dose (LD50) of fresh SA leaf homogenate was
the symptoms. The result showed some improvement in the >21.5 g/kg BW of male’s NIH mice, and the LD50 value for
severe impairment of alveolar permeability for the patient dried leaf powder was >20.0 g/kg BW of the mice [62]. All
with obstructive and restrictive lung disease that treated with mice were fed with the SA samples for 90 days. The result
SA leaves [53]. Besides, the antioxidants in SA leaves could for sub-chronic toxicity test showed that all the indexes and
prevent several chronic diseases, such as cancer and values (lymphocytes, Th1 gene expression, and blood
coronary heart disease [54]. A previous study on the biochemical parameters) were in the normal range if
determination of alpha-tocopherol contents in 62 edible supplemented with the fresh leaf homogenate. Although the
tropical plants reported the leaves of SA have the highest toxicity level of SA leaves is low, the leaves may contain
concentration (426.8 mg/kg edible portion) of alpha- antinutrients and heavy metals that pose adverse health
tocopherol [11]. The high alpha-tocopherol content of SA effects to the human body.
leaves signifies a potential protective effect of SA against
several chronic diseases. Antinutrients and Heavy Metals
The leaf extract of SA has a strong anticancer effect. The A study reported that SA leaves contained tannin (0.46
SA leaf extract at concentration of 200 µg/ml showed g/100 g DW) and saponin (2.84 g/100 g DW) [13]. As
complete inhibition (100%) of EBV (Epstein Barr virus) mentioned in the earlier section, the leaves contained 88.68
activation using Raji (human Burkitt's lymphoma) cells and mg tannin/100 g FW [6]. The leaves of SA also contained
without any cytotoxic effect [55]. In fact, inhibition of EBV oxalic acid (33.25 mg/100 g FW) as antinutrients [20]. These
activation suppresses tumor promoter that can cause chemical components are antinutrients, but they possessed
development of cancer [56]. Although the SA leaf extract is antimicrobial activities. Due to these chemical components
cytotoxic to cancer cell lines and Raji cells, the leaves should in SA leaves, the leaf extract is somehow toxic to NIH3T3
not be toxic to the human body. However, a study reported fibroblasts. The chemical components in the extract were
some accumulative toxicity in mice during 30 days of shown to induce apoptosis in the cells [5]. On the other hand,
feeding with SA leaves [57]. The lethal dose (LD50) of SA contamination of soil with heavy metal is the main reason for
leaves was >10.00 g/kg BW, and the higher dose increased the toxic effect of SA leaves. A previous study showed that
Health Benefits of Sauropus androgynus The Natural Products Journal, 2015, Vol. 5, No. 2 121

cadmium was detected in a few SA samples, where the obstructive disturbance in pulmonary function tests and
contamination was originated from soil [63]. marked variability in attenuation of lung parenchyma.
These patients were treated with corticosteroids and
On the contrary, SA samples obtained from different
bronchodilators but did not have improved symptoms.
locations in Indonesia showed a variation in cell cytotoxicity
for human mesenchymal stem cells [60]. The methanolic Moreover, the obstructive ventilation detected was dose
dependent. The number of cases was higher in high-dose
extract of SA sample obtained near Purwosari has the lowest
group than the low-dose group, where the total doses
cell viability (37%). However, the sample collected from
consumed per day for the 178 patients analyzed were A
East Java has a high percentage of cell viability (75%). The
(0-1799 g), 4/43=9.3%; B (1800-3599 g), 13/64=20.3%;
results obtained from this study show that geographical
C (3600-5399 g), 14/32=43.8%; D (5400-7199 g),
location is the main cause of accumulation of toxic
compounds that can reduce cell viability. 5/12=41.7%; and E (≥7200 g), 13/27=48.1%; p<0.01 [69].
One of the main causes of bronchiolitis obliterans is
Lung Injury papaverine exposure. An animal model was designed to test
the effect of papaverine on bronchiolitis obliterans using 33
An in vitro study shows that the aqueous fraction of SA Sprague-Dawley rats via intratracheal delivery of papaverine
dried powder significantly elevated the inflammatory [70]. The results showed that at day-7 of papaverine induced to
cytokine and chemokine production in monocytic lineage the rats, inflammation of peribronchial was observed. The other
cells, significantly induced apoptosis of endothelial cells, and clinical observations were extensive denudation, destruction
enhanced intraluminal obstructive fibrosis in allogeneic of the bronchial mucosa, and increased peribronchial collagen
trachea allograft in the murine bronchiolitis obliterans (all classic signs of chronic bronchiolitis obliterans). The
syndrome’s model [64]. The study also reported that damage worsened after 28 days of papaverine induced to the
consumption of SA leaves stimulated production of TNF-α rats. Besides that, TGF-β and eNOS of the lung homogenates
in monocytes of healthy controls and induced a high-level were significantly increased. Based on the results obtained,
production of TNF-α from monocytes of patients who the study suggested that the papaverine-induced model
consumed SA leaves. implicates the pulmonary process of collagen remodeling.
Besides the in vitro studies, the outbreak of lung diseases
or bronchiolitis obliterans is known to be associated with CONCLUSION
intake of SA leaves [65]. Several cases of obstructive S. androgynus is the medicinal plant that contains a fairly
ventilatory impairment and bronchiolitis obliterans have high amount of bioactive antioxidants. These antioxidants,
been found to associate with the consumption of SA leaves including phenolic compounds, carotenoids, anthocyanins,
in Taiwan [66] and Japan [67]. The outbreak of obstructive some volatile compounds, and other phytochemicals have
ventilatory defect among 44 Taiwanese was reported by Lin high free radical scavenging activities, thus inhibit oxidative
et al. [66] between August 23, 1994 and August 25, 1995. stress. Inhibition of oxidative stress by these antioxidants can
They suffered from typical symptoms, including temporary prevent inflammation and the onset of several chronic
insomnia, poor appetite, and breathing difficulty after intake diseases. The bioactives from S. androgynus leaves also
of SA leaves for four weeks or more. Out of the 44 patients, possess antimicrobial and anticancer effects. These
93.2% of them were women who consumed SA leaves as a bioactives may somehow pose adverse health effect to the
vegetable. human body because some of the compounds are toxic.
Another hospital-based case-control study that performed Intake of fresh leaves of SA for the potential health
in southern Taiwan between April and September 1995 benefits is not advisable as the past evidences reveal several
revealed an outbreak of a poorly defined respiratory illness outbreaks of bronchiolitis obliterans. Therefore, proper
associated with intake of SA leaves [68]. The results showed preparation of the leaves is needed prior to consumption for
that among the 54 cases and 54 self-referred patron controls, any purposes. Hype or scientific-based evidences for the
several factors were reported to associate with bronchiolitis potential health benefits from the intake of S. androgynus
obliterans syndrome. These included methods of food leaves? Consumers should make the right decision.
prepared from SA leaves [uncooked juice vs. stir fried or
boiled dishes, matched OR 10.3 (95% confidence interval of CONFLICT OF INTEREST
1.3-84.4)], person who prepared the SA leaves-containing
food [vendor only vs. patient only or patient plus vendor, The authors confirm that this article content has no
matched OR 2.8 (95% Cl 1.1–7.1)], total consumption of SA conflict of interest.
leaves [>4, 500 vs. 413–2063 g, matched OR 10.0 (95% Cl
1.9–53.0)], duration of consumption of SA leaves [>45 vs. ACKNOWLEDGEMENTS
6–24 days, matched OR 2.1 (95% Cl 1.2–3.8)], and midterm Declared none.
interruption [<2 vs. 2–5 days per week, matched OR 2.6
(95% Cl 1.1–6.1)]. The study concluded that SA leaves- REFERENCES
containing food prepared without cooking and prepared by
[1] Tatagar, M. Ecology and Management of Chili Insect Pests and
the vendor were significantly associated with bronchiolitis Pesticide Residue Estimation. PhD Thesis, University of
obliterans syndrome. Agricultural Sciences: Karnataka, India, 2010.
[2] Christi, V.E.I. Study of pharmacognostical, anti-inflammatory and
In Japan, five cases of SA-associated bronchiolitis antioxidant activity of “Saropus androgynus” plant. Int. J. Adv.
obliterans are reported [67]. All the patients have a severe Pharm. Res., 2014, 5(3), 198-207.
122 The Natural Products Journal, 2015, Vol. 5, No. 2 Khoo et al.

[3] Ong, H.C. Vegetables: Food & Medicine Properties (Khasiat [25] Badami, S.; Channabasavaraj, K.P. In vitro antioxidant activity of
Makanan & Ubatan); Utusan Publications, Kuala Lumpur, 2003. thirteen medicinal plants of India's Western Ghats. Pharm. Biol.,
(Malay) 2007, 45(5), 392-396.
[4] Handayani, L.; Suparto, H.; Suprapto, A. In: Traditional Medicine [26] Hulshof, P.J.M.; Xu, C.; van de Bovenkamp, P.; Muhilal; West,
in Asia; Chaudhury, R.R.; Rafei, U.M., Eds.; SEARO Regional C.E. Application of a validated method for the determination of
Publications No. 39, World Health Organization, 2001; pp. 47-68. provitamin A carotenoids in Indonesian foods of different maturity
[5] Yu, S.F.; Chen, T.M.; Chen, Y.H. Apoptosis and necrosis are and origin. J. Agric. Food Chem, 1997, 45(4), 1174-1179.
involved in the toxicity of Sauropus androgynus in an in vitro [27] Fatimah, A.M.Z.; Norazian, M.H.; Rashidi, O. Identification of
study. J. Formosan Med. Assoc., 2007, 106(7), 537-547. carotenoid composition in selected 'ulam' or traditional vegetables
[6] Singh, S.; Singh, D.R.; Salim, K.M.; Srivastava, A.; Singh, L.B.; in Malaysia. Int. Food Res. J., 2012, 19(2), 527-530.
Srivastava, R.C. Estimation of proximate composition, [28] Liu, Y.; Perera, C.O.; Suresh, V. Comparison of three chosen
micronutrients and phytochemical compounds in traditional vegetables with others from South East Asia for their lutein and
vegetables from Andaman and Nicobar Islands. Int. J. Food Sci. zeaxanthin content. Food Chem., 2007, 101(4), 1533-1539.
Nutr., 2011, 62(7), 765-773. [29] Yu, S.F.; Shun, C.T.; Chen, T.M.; Chen, Y.H. 3-O-β-D-glucosyl-
[7] Padmavathi, P.; Rao, M.P. Nutritive value of Sauropus androgynus (1→6)-β-D-glucosyl-kaempferol isolated from Sauropus
leaves. Plant Food Hum. Nutr., 1990, 40(2), 107-113. androgenus reduces body weight gain in Wistar rats. Biol. Pharm.
[8] Kanchanapoom, T.; Chumsri, P.; Kasai, R.; Otsuka, H.; Yamasaki, Bull., 2006, 29(12), 2510-2513.
K. Lignan and megastigmane glycosides from Sauropus [30] Sadhu, S.K.; Khatun, A.; Phattanawasin, P.; Ohtsuki, T.; Ishibashi,
androgynus. Phytochem., 2003, 63(8), 985-988. M. Lignan glycosides and flavonoids from Saraca asoca with
[9] Miean, K.H.; Mohamed, S. Flavonoid (myricetin, quercetin, antioxidant activity. J. Nat. Med., 2007, 61(4), 480-482.
kaempferol, luteolin, and apigenin) content of edible tropical [31] Wang, P.H.; Lee, S.S. Active chemical constituents from Sauropus
plants. J. Agric. Food Chem., 2001, 49(6), 3106-3112. androgynus. J. Chin. Chem. Soc., 1997, 44(2), 145-149.
[10] Andarwulan, N.; Batari, R.; Sandrasari, D.A.; Bolling, B.; Wijaya, [32] Yang, R.Y.; Lin, S.; Kuo, G. Content and distribution of flavonoids
H. Flavonoid content and antioxidant activity of vegetables from among 91 edible plant species. Asia Pac. J. Clin. Nutr., 2008,
Indonesia. Food Chem., 2010, 121(4), 1231-1235. 17(S1), 275-279.
[11] Ching, L.S.; Mohamed, S. Alpha-tocopherol content in 62 edible [33] Gayathramma, K.; Pavani, K.V.; Raji, R. Chemical constituents
tropical plants. J. Agric. Food Chem., 2001, 49(6), 3101-3105. and antimicrobial activities of certain plant parts of Sauropus
[12] Tangkanakul, P.; Trakoontivakorn, G.; Auttaviboonkul, P.; androgynus L. Int. J. Pharm. Biol. Sci., 2012, 3(2), B-561-B-566.
Niyomvit, B.; Wongkrajang, K. Antioxidant activity of Northern [34] Lin, C.; Lin, W.; Pan, W.; Li, Y. Study on chemical constituents of
and Northeastern Thai foods containing indigenous vegetables. the essential oil from the leaves of Sauropus androgynus (L.) Merr.
Kasetsart J. (Natural Science), 2006, 40, 47-58. J. Tropic. Subtropic. Botan., 1998, 7(3), 255-256.
[13] Hermana, W. Evaluation of Usage Katuk (Sauropus androgynus) [35] Selvi, S.V.; Basker, A. Phytochemical analysis and GCMS
and Mulberry Leaves Meal (Morus alba) on Productivity and profiling in the leaves of Sauropus androgynous (L) Merr. Int. J.
Physiology Status of Laying Quail. PhD Thesis, Bogor Agricultural Drug Dev. Res., 2012, 4(1), 162-167.
University: Indonesia, 2013. (Indonesian) [36] Ogle, B.M.; Hung, P.H.; Tuyet, H.T. Significance of wild vegetables
[14] Maisuthisakul, P.; Pasuk, S.; Ritthiruangdej, P. Relationship in micronutrient intakes of women in Vietnam: an analysis of food
between antioxidant properties and chemical composition of some variety. Asia Pac. J. Clin. Nutr., 2001, 10(1), 21-30.
Thai plants. J. Food Compos. Anal., 2008, 21(3), 229-240. [37] Gudkov, S.V.; Shtarkman, I.N.; Smirnova, V.S.; Chernikov, A.V.;
[15] Andarwulan, N.; Kurniasih, D.; Apriady, R.A.; Rahmat, H.; Roto, Bruskov, V.I. Guanosine and inosine display antioxidant activity,
A.V.; Bolling, B.W. Polyphenols, carotenoids, and ascorbic acid in protect DNA in vitro from oxidative damage induced by reactive
underutilized medicinal vegetables. J. Funct. Foods, 2012, 4(1), oxygen species, and serve as radioprotectors in mice. Rad. Res.,
339-347. 2006, 165(5), 538-545.
[16] Ogle, B.M.; Dao, H.T.A.; Mulokozi, G.; Hambraeus, L. [38] Madhu, C.S.; Manukumar, H.M.G. New-vista in finding
Micronutrient composition and nutritional importance of gathered antioxidant and anti-inflammatory property of crude protein extract
vegetables in Vietnam. Int. J. Food Sci. Nutr., 2001, 52(6), 485- from Sauropus androgynus leaves. Acta Sci. Pol. Technol.
499. Aliment., 2014, 13(4), 375-383.
[17] Hoe, V.B.; Siong, K.H. The nutritional value of indigenous fruits [39] Murti, S.; Abidin, N.Z.; Yusof, A. Antioxidant activity in crude
and vegetables in Sarawak. Asia Pac. J. Clin. Nutr., 1999, 8(1), 24- petroleum benzene, chloroform, methanol and water extracts of six
31. selected vegetables. Sains Malay., 2013, 42(9), 1253-1259.
[18] Petrus, A.J.A. Sauropus androgynus (L.) Merrill-A potentially [40] Maisuthisakul, P. In: Phytochemicals-A Global Perspective of
nutritive functional leafy-vegetable. Asian J. Chem., 2013, 25(17), Their Role in Nutrition and Health; Rao, V., Ed.; InTech: Croatia,
9425-9433. 2012; pp.187-212.
[19] Samuelsson, A.; Sjödin, R. Dietary Intake of Zinc and Iron Within [41] Allen, T.C. Pathology of small airways disease. Arch. Pathol. Lab.
the Female Population of Two Farming Villages in the Red River Med., 2010, 134(5), 702-718.
Delta, Vietnam; No. 339, Department of Food Science, Swedish [42] Hung, G.U.; Tsai, S.C.; Hsieh, J.F.; Kao, C.H.; Wang, S.J. Detect
University of Agricultural Sciences. http://stud.epsilon.slu.se/ bronchiolitis obliterans due to Sauropus androgynus vegetable
4098/7/samuelsson_a_%20renee_s_120419.pdf (Accessed October ingestion: comparison with 99mTc-DTPA radioaerosol inhalation
24, 2014). lung scintigraphy, high resolution computed tomography and
[20] Sheela, K.; Nath, K.G.; Vijayalakshmi, D.; Yankanchi, G.M.; pulmonary function testing. Ann. Nucl. Med. Sci., 2000, 13, 197-
Patil, R.B. Proximate composition of underutilized green leafy 202.
vegetables in Southern Karnataka. J. Hum. Ecol., 2004, 15(3), 227- [43] Orech, F.O.; Akenga, T.; Ochora, J.; Friis, H.; Aagaard-Hansen, J.
229. Potential toxicity of some traditional leafy vegetables consumed in
[21] Sripanidkulchai, B.; Homhual, S.; Poeknapo, C. Analysis of Nyang’oma Division, Western Kenya. Afr. J. Food Agric. Nutr.
antioxidant vitamins in 30 Thai vegetables by high-performance Dev., 2005, 5(1), 1-13.
liquid chromatographic method. Isan J. Pharm. Sci., 2014, 1(2), [44] Lai, R.S.; Wang, J.S.; Lee, P.C. Sauropus androgynus and
58-69. papaverine do not induce bronchiolitis obliterans in Sprague-
[22] Zeng, X.F.; Qiu, H.Y. The contents of nitrate, nitrite, and vitamin C Dawley rats. Chin. Med. J., 2000, 63(7), 536-541.
in different parts of six edible wild vegetables. Acta Bot. [45] Paul, M.; Anto, K. Antibacterial activity of Sauropus androgynus
Yunnanica, 2005, 27(3), 321-326. (Chinese) (L.) Merr. Int. J. Plant Sci., 2011, 6(1), 189-192.
[23] Wong, S.P.; Leong, L.P.; William Koh, J.H. Antioxidant activities [46] Ariharan, V.N.; Devi, V.M.; Prasad, P.N. Antibacterial activity of
of aqueous extracts of selected plants. Food Chem., 2006, 99(4), Sauropus androgynus leaves extracts against some pathogenic
775-783. bacteria. Rasayan J. Chem., 2013, 6(2), 134-137.
[24] Subhasree, B.; Baskar, R.; Laxmi Keerthana, R.; Lijina Susan, R.; [47] Selvi, V.S.; Bhaskar, A. Characterization of anti-inflammatory
Rajasekaran, P. Evaluation of antioxidant potential in selected activities and antinociceptive effects of papaverine from Sauropus
green leafy vegetables. Food Chem., 2009, 115(4), 1213-1220. androgynus (L.) Merr. Global J. Pharmacol., 2012, 6(3), 186-192.
Health Benefits of Sauropus androgynus The Natural Products Journal, 2015, Vol. 5, No. 2 123

[48] Selvi, V.S.; Baskar, A. Attenuation of cyclooxygenase and induced [60] Yunita, O.; Yuwono, M.; Rantam, F.A. In vitro cytotoxicity assay
nitric oxide synthase and antioxidant properties by Sauropus of Sauropus androgynus on human mesenchymal stem cells.
androgynus (L.) Merr. plant leaves. World J. Med. Sci., 2014, Toxicol. Environ. Chem., 2013, 95(4), 679-686.
11(3), 334-341. [61] Tjahjadi, F.I. The Influence of Katu (Sauropus androgynus (L.)
[49] Khadaroo, R.G.; Kapus, A.; Powers, K.A.; Cybulsky, M.I.; Merr.) and Papaya (Carica papaya) Leaves Consumption On
Marshall, J.C.; Rotstein, O.D. Oxidative stress reprograms Volume, Vitamin A Level and Protein Content of Breast Milk.
lipopolysaccharide signaling via Src kinase-dependent pathway in Bachelor Thesis, Universitas Indonesia: Indonesia, 1990. (Indonesian)
RAW 264.7 macrophage cell line. J. Biol. Chem., 2003, 278(48), [62] Xiong, X.K.; Yang, G.G.; Zhang, J. Evaluation of toxicity and
47834-47841. safety of Sauropus androgynus. Chinese J. Pub. Health, 2011,
[50] Bhaskar, A.; Ramesh, K.V. Wound healing profile of Sauropus 27(12), 1553-1555. (Chinese)
androgynus in Wistar rats. J. Nat. Remedies, 2009, 9(2), 159-164. [63] Yang, Y.; He, Y.S.; Mo, W.R.; Zhang, G.C.; Yin, M.S. Study on
[51] Raveendran, D.; Koshy, M.S. Evaluation of Anticonvulsant Activity eco-geochemistry of cadmium in Sauropus androgynus from
of Hydroalcoholic Extract of Sauropus androgynus Leaves. Master Wuzhishan City of Hainan Province. Rock Mineral Anal., 2007, 4,
Thesis, Srinivas College of Pharmacy: Mangalore, India, 2014. 003. (Chinese)
[52] Erman Syahruddin, R.H.; Ningrat, R.W.S. Effect of fermented [64] Hashimoto, I.; Imaizumi, K.; Hashimoto, N.; Furukawa, H.; Noda,
katuk leaves (Sauropus androgynus L. Merr.) in diets on Y.; Kawabe, T.; Honda, T.; Ogawa, T.; Matsuo, M.; Imai, N.; Ito,
cholesterol content of broiler chicken carcass. Pak. J. Nutr., 2013, S.; Sato, M.; Kondo, M.; Shimokata, K.; Hasegawa, Y. Aqueous
12(11), 1013-1018. fraction of Sauropus androgynus might be responsible for
[53] Wu, C.L.; Hsu, W.H.; Chiang, C.D.; Kao, C.H.; Hung, D.Z.; King, bronchiolitis obliterans. Respirol., 2013, 18(2), 340-347.
S.L.; Deng, J.F. Lung injury related to consuming Sauropus [65] Schlesinger, C.; Meyer, C.A.; Veeraraghavan, S.; Koss, M.N.
androgynus vegetable. Clin. Toxicol., 1997, 35(3), 241-248. Constrictive (obliterative) bronchiolitis: diagnosis, etiology, and a
[54] Fairfield, K.M.; Fletcher, R.H. Vitamins for chronic disease critical review of the literature. Ann. Diagn. Pathol., 1998, 2(5),
prevention in adults: scientific review. JAMA, 2002, 287(23), 3116- 321-334.
3126. [66] Lin, T.J.; Lu, C.C.; Chen, K.W.; Deng, J.F. Outbreak of obstructive
[55] Murakami, A.; Ali, A.M.; Mat-Salleh, K.; Koshimizu, K.; ventilatory impairment associated with consumption of Sauropus
Ohigashi, H. Screening for the in vitro anti-tumor-promoting androgynus vegetable. Clin. Toxicol., 1996, 34(1), 1-8.
activities of edible plants from Malaysia. Biosci. Biotechnol. [67] Oonakahara, K.; Matsuyama, W.; Higashimoto, I.; Machida, K.;
Biochem., 2000, 64(1), 9-16. Kawabata, M.; Arimura, K.; Osame, M.; Hayashi, M.; Ogura, T.;
[56] Murakami, A.; Toyota, K.; Ohura, S.; Koshimizu, K.; Ohigashi, H. Imaizumi, K.; Hasegawa, Y. Outbreak of bronchiolitis obliterans
Structure-activity relationships of (1'S)-1'-acetoxychavicol acetate, associated with consumption of Sauropus androgynus in Japan–
a major constituent of a southeast Asian condiment plant Languas alert of food-associated pulmonary disorders from Japan.
galanga, on the inhibition of tumor-promoter-induced Epstein-Barr Respiration, 2005, 72(2), 221.
virus activation. J. Agric. Food Chem., 2000, 48(5), 1518-1523. [68] Ger, L.P.; Chiang, A.A.; Lai, R.S.; Chen, S.M.; Tseng, C.J.
[57] Guo, J.X.; Yang, X.; Guo, L.L. Studies on the toxicology of Association of Sauropus androgynus and bronchiolitis obliterans
Sauropus androgynus, a wild vegetable in South China. J. South syndrome: a hospital-based case-control study. Am. J. Epidemiol.,
China Agric. Univ., 2005, 4, 10-14. (Chinese) 1997, 145(9), 842-849.
[58] Soka, S.; Alam, H.; Boenjamin, N.; Agustina, T.W.; Suhartono, M. [69] Hsiue, T.R.; Guo, Y.L.; Chen, K.W.; Chen, C.W.; Lee, C.H.;
T. Effect of Sauropus androgynus leaves extracts on the expression Chang, H.Y. Dose-response relationship and irreversible obstructive
of prolactin and oxytocin genes in lactating BALB/c mice. J. ventilatory defect in patients with consumption of Sauropus
Nutrigenet. Nutrigenomics, 2010, 3(1), 31-36. androgynus. CHEST J., 1998, 113(1), 71-76.
[59] Sa'roni, S.R.; Sadjiman, T.; Sja'bani, M.; Zulaela, Z. Effectiveness [70] Svetlecic, J.; Molteni, A.; Herndon, B. Bronchiolitis obliterans
of the Sauropus androgynus (L.) Merr leaves extract in increasing induced by intratracheal papaverine: a novel animal model. Lung,
mother’s breast milk production. Media Health Res. Dev., 2004, 2004, 182(2), 119-134.
14(3), 20-24. (Indonesian).

Received: April 02, 2015 Revised: May 28, 2015 Accepted: May 30, 2015

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