Evidence-Based Complementary and Alternative Medicine
Volume 2015 (2015), Article ID 714158, 7 pages
http://dx.doi.org/10.1155/2015/714158

Review Article

Sauropus androgynus (L.) Merr. Induced Bronchiolitis Obliterans: From Botanical Studies to Toxicology

Hamidun Bunawan,¹ Siti Noraini Bunawan,² Syarul Nataqain Baharum,¹ and Normah Mohd. Noor¹

¹Institute of Systems Biology, Universiti Kebangsaan Malaysia, 43600 Bangi, Selangor Darul Ehsan, Malaysia
²Biotechnology Research Centre, Malaysian Agricultural Research and Development Institute, P.O. Box 12301, 50774 Kuala Lumpur, Malaysia

Received 3 March 2015; Revised 29 July 2015; Accepted 4 August 2015

Academic Editor: Shun-Wan Chan

Copyright © 2015 Hamidun Bunawan et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Sauropus androgynus L. Merr. is one of the most popular herbs in South Asia, Southeast Asia, and China where it was known as a slimming agent until two outbreaks of pulmonary dysfunction were reported in Taiwan and Japan in 1995 and 2005, respectively. Several studies described that the excessive consumption of Sauropus androgynus could cause drowsiness, constipation, and bronchiolitis obliterans and may lead to respiratory failure. Interestingly, this herb has been used in Malaysia and Indonesia in cooking and is commonly called the “multigreen” or “multivitamin” plant due to its high nutritive value and inexpensive source of dietary protein. The plant is widely used in traditional medicine for wound healing, inducing lactation, relief of urinary disorders, as an antidiabetic cure and also fever reduction. Besides these medicinal uses, the plant can also be used as colouring agent in food. This review will explore and compile the fragmented knowledge available on the botany, ethnobotany, chemical constitutes, pharmacological properties, and toxicological aspects of this plant. This comprehensive review will give readers the fundamental, comprehensive, and current knowledge regarding Sauropus androgynus L. Merr.

1. Introduction

Sauropus androgynus L. Merr. is a shrubby plant belonging to the Euphorbiaceae family. It grows in humid, high temperature conditions and is a Southeast Asian indigenous vegetable, widely cultivated for traditional medicinal purposes. S. androgynus is known as Star gooseberry, Sweet leaf bush, Phak waan baan in Thailand, Cekur manis in Malaysia, Katuk in Indonesia, Binahian in Philippines, and Dom nghob in Cambodia.

In Malaysia, this plant is used in traditional medicine to relieve fever, treat urinary problems, and increase breast milk production and consumed as salad, prepared as curry, or stir-fried. It is known as “multigreen” vegetable due to its perceived superior nutrition and vitamin content in comparison to other vegetables [1, 2]. S. androgynus was reported to have approximately 7.4 g protein per 100 g of fresh leaves whilst, for comparison, spinach has 2.0 g, mint 4.8 g, and cabbage about 1.8 g [1]. The vitamin and mineral composition in S. androgynus is summarized in Table 1.

Table 1: Nutrition assessment of Sauropus androgynus content in 100 g of fresh leaves.

Value
Value

Protein
7.4 g
5.25 g

Fat
1.1 g
0.58 g

Fibre
1.8 g
1.75 g

Moisture
69.9 g
85.4 g

Carotene
5600 g
—

Riboflavin
0.21 mg
—

Thiamine
0.50 mg
—

Potassium
—
45.7 mg

Cobalt
—
1.62 mg

Manganese
—
25.6 mg

Copper
—
768.7 mg

Sodium
—
306.3 mg

Zinc
—
15.9 g

Fe
—
212.5 mg

Magnesium
—
664.9 mg

Calcium
711 mg
84.4 mg

Vitamin C
244 mg
314.3 mg

Phosphorus
543 mg
—

Iron
8.8 mg
—

Based on the proximate composition studied by Padmavathi and Rao [1] and Singh et al. [2].

Despite its use as a medicinal and food product, several studies have reported pulmonary dysfunction as a side effect of consuming S. androgynus. The first study on the toxic effects of S. androgynus was conducted by Bender and Ismail [3]. The study found that unnecessary ingestion of this plant by the elderly in Malaysia caused drowsiness and constipation, demonstrating that the fresh leaves of S. androgynus contain 580 mg of alkaloid “papaverine” per 100 gram, and an excessive amount considering only 200 mg of papaverine per day is required as an antispasmodic drug [1, 3]. The first details of problems caused by excessive consumption of S. androgynus occurred in Taiwan in 1995 after S. androgynus was introduced as supplement to reduce weight in 1994 [4]. Cases of difficulty of breathing were reported, as well as irreversible respiratory failure and death following ingestion of S. androgynus. Histopathological examinations found that those patients were diagnosed with constrictive bronchiolitis obliterans and lung transplantation was the only way to treat the condition [5–9].

Due to the impact of this plant on the human consumption, this review will focus on collating the fragmented information regarding botany, chemical composition, pharmacological effects, and toxicology of S. androgynus, highlighting the current state of knowledge and providing an intensive overview to readers and researchers.

2. Botany

2.1. Botanical Name

It is called Sauropus androgynus (L.) Merr.

2.2. Synonyms

Aalius androgyna (L.) Kuntze; Aalius lanceolata (Hook.f.) Kuntze; Aalius oblongifolia (Hook.f.) Kuntze; Aalius retroversa (Wight) Kuntze; Aalius sumatrana (Miq.) Kuntze; Agyneia ovata Poir.; Andrachne ovata Lam. ex Poir.; Clutia androgyna L.; Phyllanthus strictus Roxb.; Sauropus albicans Blume; Sauropus albicans var. gardnerianus (Wight) Müll.Arg.; Sauropus albicans var. intermedius Müll.Arg.; Sauropus albicans var. zeylanicus (Wight) Müll.Arg.; Sauropus convexus J.J.Sm.; Sauropus gardnerianus Wight; Sauropus indicus Wight; Sauropus lanceolatus Hook.f.; Sauropus oblongifolius Hook.f.; Sauropus parviflorus Pax & K.Hoffm.; Sauropus retroversus Wight; Sauropus scandens C.B.Rob.; Sauropus sumatranus Miq.; Sauropus zeylanicus Wight [10].

2.3. Botanical Description and Distribution

Sauropus androgynus is an erect shrub that can reach up to 500 cm in height. It is flaccid and has cylindrical or angled branches (Figure 1). The leaves are ovate or lance-shaped, measuring 2.0–7.5 cm and obtuse or acute. The male flowers are disk-shaped, entirely or nearly so. The fruit is nearly globular, up to 1.5 cm in diameter and whitish [10]. This plant is widely cultivated and native to Southeast Asia including Bangladesh, India, Guangdong, Guangxi, Hainan, and Yunnan [10].

Figure 1: Sauropus androgynus L. Merr., also known to Malaysian as Cekur Manis.

3. Ethnobotanical Uses

Sauropus androgynus has been known as “multigreen” due to its high vitamin and nutrient content and this vegetable is usually consumed raw in salad, stir-fried, used in curry, or cooked in soups in most countries in Southeast Asia. Also, S. androgynus is believed to increase lactation in women in Indonesia and Malaysia [11, 12]. Furthermore, Thai people traditionally use the roots of this plant to reduce fever and treat food poisoning and as antiseptic agent [1, 13]. People in Taiwan believe that S. androgynus could have significant potential as a slimming agent to combat obesity. In India, the leaves of this plant are used as antidiabetic and to improve vision. Traditional uses of S. androgynus are summarized in Table 2.

Table 2: Ethnobotanical uses of Sauropus androgynus L. Merr.

Uses
Locality
Reference

A medication for coughs, to soothe lungs, as a tonic to reduce fever, a natural slimming agent, and consumption as a vegetable.
China
[10]

To increase milk production, as an antipyretic, consumed as a vegetable and used as a colorant.
Indonesia
[11, 12, 47]

The roots are used to reduce fever and to reduce food poisoning and as an antiseptic.
Thailand
[1, 13]

The roots are used to treat cardiovascular diseases and hypertension. The leaves are used to increase lactation and for treatment of oral thrush of infants as well as an eye lotion.
Malaysia
[48, 49]

Leaves are used as an antidiabetic, to treat ulcers, eye disease, and tonsillitis.
India
[21, 50]

To improve vision and to treat eye diseases.
Southeast Asia inhabitants
[51]

4. Chemical Compositions

Phytochemical investigation of the leaves of S. androgynus reveals they contained sterols, resins, tannins, saponins, alkaloids, flavonoids, terpenoids, glycosides, phenols, catechol, cardiac glycosides, and acidic compounds [14]. Previously, preliminary phytochemical screening on the leaves of S. androgynus showed polyphenols, anthocyanins, carotenoids, ascorbic acids, and tannins [2]. Further phytochemical studies by Gireesh et al. [15] suggested that the leaf ethanol and aqueous extracts of S. androgynus contain tannins, saponins, flavonoids, terpenoids, phenolics, steroids, and alkaloids. These preliminary phytochemical studies suggested that S. androgynus contains a wide range of biomolecules constituents that might contribute to its medicinal, toxic, and antioxidant properties.

Wang and Lee [16] isolated six compounds (three nucleosides, two flavonol diosides, and one compound flavonol trioside) based on spectral analysis from butanol extract of S. androgynus leaves. One of the novel isolated compounds, known as 3-O-β-D-glucosyl-(1-6)-β-D-glucosyl-kaempferol (GGK), was reported to have a high potential as an antiobesity agent [17]. A study by Kanchanapoom et al. [18] elucidated and identified seven bioactive compounds from the methanolic extract of the aerial part of S. androgynus, including three lignan glycosides, a lignan diglycoside, a megastigmane glucoside, and a megastigmane glucoside compound. S. androgynus leaves were found to have highest content of flavonoids and bioactive compounds among 11 vegetables from Indonesia with 142.64 mg per 100 gram of fresh weight with quercetin, myricetin, luteolin, apigenin, and kaempferol which were detected by HPLC analysis [12, 19]. Further, phenolic acids such as chlorogenic acid, caffeic acid, and ferulic acid were also identified in their study.

Selvi and Basker [20] found occurrences of phytol and squalene in ethanolic extract of S. androgynus using gas chromatography-mass spectrometry (GC-MS) analysis. Further analysis on ethanolic S. androgynus leaves extract by GC-MS discovered nine compounds with medicinal functionality such as antimicrobial, anti-inflammatory, antioxidant, and anticancer properties [14].

5. Pharmacological Properties

5.1. Antidiabetes Activity

Sai and Srividya [21] presented an experiment which focused on the evaluation of the effects of aqueous leaf digest of S. androgynus on the postprandial glucose levels in human blood. The results show that glycemic index (GI) scores for patients that were administered the S. androgynus leaf digest were significantly lower compared to the control group. This result suggests that this plant possesses a high potential for lowering glucose levels in human blood, which would likely assist in the global battle to reduce diabetes.

5.2. Antiobesity Effect

High consumption of young leaves of S. androgynus over a long period in the belief that the plant helps to maintain weight resulted in a sudden increase of bronchiolitis obliterans in Taiwan, which is normally rare life-threatening lung disease. The believe that S. androgynus had values as an antiobesity agent was confirmed in a study by Yu et al. [17], which focused on effects of S. androgynus isolated GGK compound in combination with EtOAc and n-BuOH fractions for body weight reduction in Wistar male rats. The results show that 60 mg per kg dose of GGK led to a decrease of food intake of rats by 15% and this led to a reduction in body weight of these rats. This loss of food intake directly corresponded to doses of GGK administered to different groups of rats. Further, no histopathological changes were observed. It was concluded that GGK has a potential to become an antiobesity agent and is unlikely to result in similar side effects as observed when consuming the entire plant.

5.3. Wound-Healing Activity

A test demonstrating wound-healing activities of 5% water extract of S. androgynus with both male and female rats was reported by Bhaskar et al. [22]. The study found that S. androgynus considerably increased contraction of wounds, reepithelization, and wound breaking strength. Histological testing of wound tissue was also reported, and smaller macrophages and fibroblasts, as well as rich collegenation, were observed in comparison to the rat control group. Based on these findings it can be concluded that S. androgynus has potential as a wound-healing agent and further research could be conducted to bring this type of produce to market.

5.4. Anti-Inflammatory Activity

Anti-inflammatory activity of S. androgynus was reported by Senthamarai Selvi and Bhaskar [23]. The study evaluated the effect of ethanolic and aqueous leaf extracts of this herb on Wister rats using carrageenan induced rat paw edema. The ethanolic extract showed a higher anti-inflammatory effect than aqueous extract. This was supported by another study on in vitro anti-inflammatory properties of the methanolic extract of this plant, showing significant nitric oxide inhibitory activity using Griess assay [24].

5.5. Induction of Lactation Activity

An experiment was performed to verify the effect of S. androgynus on production of breast milk as it is commonly consumed for this purpose in Indonesia. House mice (Mus musculus) were used for this test and were divided into groups and administered leaf extract of fully grown S. androgynus in various dosages [11]. The study found that both expressions of the oxytocin gene and prolactin gene expression levels remarkably increased according to the amount of S. androgynus administered. The administration of the extract resulted in smoother circulation of the oxytocin hormone in the mouse bloodstream. Based on the experiment by Soka et al. [11], S. androgynus was found to have beneficial effect on breast milk production in mice and could become a breast milk production agent subject to future research.

5.6. Antioxidant Activity

Several studies reported positive antioxidant activity of S. androgynus [14, 19, 25]. A study conducted by Andarwulan et al. [19] implies potential of this herb to become a strong antioxidant agent. This plant was found to have highest flavonoid content among 11 vegetables of Indonesian origin. Another experiment done by Badami and Channabasavaraj [25] used methanol extracts of this herb using several in vitro free radical-scavenging assays. The study found that S. androgynus has IC₅₀ value of 341 μg/mL, 12.58 μg/mL, and 228.75 μg/mL using DPPH radicals, ABTS cation radicals, and inhibition of lipid peroxidation, respectively. A previous study on antioxidant activities on aqueous extracts of 25 tropical plants showed that S. androgynus has a high polyphenol content, cupric ion chelating activities, free radical scavenging, and reducing ferric ion antioxidant properties [26].

5.7. Antimicrobial Activity

Methanolic and ethanolic extracts of S. androgynus have been reported to have significant antibacterial activity against Bacillus cereus, Proteus vulgaris, and Staphylococcus aureus [27]. On the other hand, aqueous extract demonstrated moderate antibacterial ability. This was later confirmed by Ariharan et al. [28]. The study also found that methanol extract significantly showed increased antibacterial activity compared with aqueous extract against gram positive bacteria. A further study found that ethanol extracts of S. androgynus produced higher antibacterial effects against Klebsiella pneumonia and S. aureus in comparison to aqueous extracts [29]. The extracts of S. androgynus were also found to have antifungal inhibitory effects against several fungi such as Aspergillus flavus and Candida albicans [30].

6. Toxicity of Sauropus androgynus

In vitro cytotoxicity and genotoxicity of this herb were studied by Xin et al. [31] who examined cooked and uncooked leaf juice of S. androgynus on CHL cells. Effects of these juices were observed at various concentrations for CHL cells which were exposed to the juice for one to three days. The study found that this herb effects two components inside of the cells (obliteration to lysosomes and golgi apparatus) when administered in certain doses; however, no chromosome changes were perceived as a result of administration of S. androgynus.

Further study on the toxicity of this plant has been done by Yu et al. [32], with use of polarity dissection, dividing the extract of S. androgynus into three different fractions (-BuOH fraction, CHCI₃ fraction, and EtOAc). NIH3T3 fibroblasts cells were exposed to these fractions at concentration of 300 μg/mL and tested for toxicity. The results showed that the EtOAc fraction has the leading effect on cell growth inhibition and more importantly that apoptosis and necrosis are present when all the extracts are applied to NIH3T3 fibroblasts. Additional safety assessments on this plant have been conducted using human cell lines MRC-5 and Hep G2 treated with raw S. androgynus homogenate at various doses for 24 hours [33]. The homogenate of S. androgynus was found to be more toxic on MRC-5 cells (IC₅₀: 133.1 mg/mL), the cells derived from human lung compared to Hep G2 cells (IC₅₀: 185.1), and cell line derived from liver tissue. In contrast, S. androgynus does not contribute to the genetic damage using micronuclei test [33].

Recently, Yunita et al. [34] evaluated methanol leaves extracts of the S. androgynus from six different parts of East Java Province, Indonesia, on human mesenchymal stem cells, the cells originating from bone marrow. Surprisingly, S. androgynus methanol extract was found to be less cytotoxic to the cells tested with IC₅₀ 2450 mg/L. However, the methanol extracts displayed an effect on the viability of the cells that might contribute to cytotoxicity of this plant. To our knowledge, there is no in vivo toxicology test that has been conducted to clarify the toxic effects, the period of the effects, and severity and degree of reversibility of this plant. Despite having many positive effects on human health as a multigreen and multivitamin plant, consumption of S. androgynus is often connected to bronchiolitis obliterans.

7. Sauropus androgynus Induced Bronchiolitis Obliterans

The connection between the consumption of the herb and potentially deadly bronchiolitis obliterans (BO) was discovered shortly after S. androgynus was introduced in Taiwan as a weight reduction agent in 1994 [4]. An outbreak of Sauropus androgynus induced bronchiolitis obliterans was reported in Taiwan in 1995 with approximately 278 patients diagnosed after consumption of uncooked S. androgynus [4, 35]. A total of nine patients died and lung transplantation was the only option for treatment of this problem [4, 36, 37]. According to Bender and Ismail [3], leaves of S. androgynus contain papaverine as its main toxic component and this compound was found to induce pulmonary disease in animal studies [38]. Wu et al. [5] describe papaverine as a smooth muscle relaxant and vasodilator with recommended intake of 300 mg a day in doses of 150 mg every 12 hours. Those consuming 600 grams of leaves would achieve an intake of 3480 mg weekly. Adverse reactions to the substance are skin rash, abdominal pains, hepatotoxicity, flushing, headache, tachycardia, and dizziness.

Common symptoms of BO disease are firstly palpitation and insomnia, leading to further symptoms which are tightness in chest and dyspnea and many patients were also reported to suffer from respiratory distress. Once these symptoms develop, spirometry and lung biopsy specimens are found to have obstructive ventilatory problems that mean that BO disease was induced. Lai et al. [4] claim that, during a two-year period after having been infected with BO, pulmonary deterioration and even death in 7 of 115 cases (6.1% of patients) occurred. The pathogenesis of S. androgynus-associated BO is still unknown. However, it is not an infectious disease. While most patients’ status remained stable with cough and dyspnea, about a fifth of them recorded decreasing respiratory function; some even developed a failure and became dependant on ventilators.

Hung et al. [39] demonstrated possible ways of detecting this disease. Methods such as pulmonary function tests and high-resolution computed tomography can help to discover diffuse bronchiectasis as well as mosaic attenuation. With the use of radioaerosol lung scans, signs such as inhomogeneous distribution of aerosol or higher alveolar permeability can be observed. High-resolution computed tomography is a method which has been proven to be very useful with detection of BO and also patchy low attenuation with mosaic perfusion. The main advantage of this method is in fact that it helps to specify this particular disease and prevents it from being mistaken for other respiratory lung diseases. Another useful method is a DTPA lung scan. It was initially used to evaluate lung status of patients after S. androgynus intake. A high variety of abnormalities were found which was observed as inhomogeneous aerosol distribution and impaired lung epithelial permeability. This is particularly useful for gathering information about ventilation of lungs; the clearance of DTPA also shows alveolar epithelial permeability.

Many different medications have been administered to patients suffering from S. androgynus-induced BO in an attempt to improve their condition. Cytotoxic agents and steroids, as well as other immunosuppressive agents, have been tried in order to reduce the effects of the disease and ease the symptoms. Unfortunately, no patient with the advanced stage of the disease has shown signs of improvement. Patients in advanced stage of the illness usually become dependent on ventilators which are difficult to regulate due to airway obstructions and then patients die due to respiratory failure. Complete lung transplantation seems to be the only solution for patients in advanced stage of the disease [40, 41].

7.1. Papaverine: An Alkaloid in Sauropus androgynus Responsible for Bronchiolitis Obliterans

Little is known regarding how ingested S. androgynus induces bronchiolitis obliterans [42]. In general, the bronchiectasis and mosaic attenuation were present in patients consuming high level of the alkaloid papaverine in Sauropus androgynus [5, 7, 40, 43]. Inflammation in small airways and fibrotic lesions of the bronchioles were also observed as well as narrowing of their lumens [44]. Intratracheal papaverine was reported to induce constrictive bronchiolitis obliterans (CBO) in an animal model [42]. On the seventh day after the start of administering papaverine to rats using intratracheal papaverine method, animals started to show common symptoms of CBO. These included extensive denudation, peribronchial inflammation, bronchial mucosa degradation, and an increase in peribronchial collagen [42]. Further, after four weeks of administration of papaverine, the toxicant induced model produced further severe disruption in rats bodies. In papaverine treated animals, two cytokines deregulated in human CBO, TGF-β and eNOS, were found at significantly high levels. These cytokines might be responsible for pathogenesis of CBO in humans, which leads to the harmful pulmonary changes connected to CBO.

The study reported by Svetlecic et al. [42] also found that the rats that received papaverine for four weeks had a high level of TGF-β in the lung homogenate supernatant. This finding matches with studies that found TGF-β immunohistochemically in humans with transplant induced BO [45]. As a marker of airway fibrous obliteration, TGF-β induced fibrosis leads to airway constriction and luminal obliteration. Endothelial nitric oxide synthase (eNOS) was also found to be significantly high in rats that received papaverine treatment for 1 to 4 weeks [42]. This enzyme is important for both destruction of the epithelium and stimulation of fibroblast assay in animal model [46]. In humans, it is generally expressed in airway epithelium of human transplant induced CBO. The significant increase of TGF-β and eNOS in animal models induced by papaverine suggests that papaverine has the potential to induce bronchiolitis obliterans and this reflects the mechanism observed in humans [42].

8. Conclusions

Sauropus androgynus is a traditional medicinal plant used in Southeast Asia, especially in Malaysia known as a green multivitamin herb. Previous studies have reported the prospective of this plant as antioxidant, antimicrobial, wound-healing, anti-inflammatory, antidiabetic, and antiobesity agent as well as its potential to increase breast milk production. Despite these pharmacological properties, consumption of its raw leaf juice for weight reduction resulted in outbreak of bronchiolitis obliterans. It seems that papaverine is the chemical compound responsible for occurrence of this pulmonary failure. Further studies should be made in order to fully understand the cytotoxicity of this plant, mechanism of toxicity, dosages and ways of consumption, and effects on human health.

Conflict of Interests

The authors declare no conflict of interests.

Acknowledgments

The authors would like to thank Lukas Dusik, Kathryn Ford, and Dr. Scott Hayes from School of Biological Sciences, University of Bristol, for their critical editorial comments on this paper.

References

P. Padmavathi and M. P. Rao, “Nutritive value of Sauropus androgynus leaves,” Plant Foods for Human Nutrition, vol. 40, no. 2, pp. 107–113, 1990.

S. Singh, D. R. Singh, K. M. Salim, A. Srivastava, L. B. Singh, and R. C. Srivastava, “Estimation of proximate composition, micronutrients and phytochemical compounds in traditional vegetables from Andaman and Nicobar Islands,” International Journal of Food Sciences and Nutrition, vol. 62, no. 7, pp. 765–773, 2011.

A. E. Bender and K. S. Ismail, “Nutritive value and toxicity of Sauropus androgynous,” The Proceedings of the Nutrition Society, vol. 32, no. 2, pp. 79A–80A, 1973.

R.-S. Lai, A. A. Chiang, M.-T. Wu et al., “Outbreak of bronchiolitis obliterans associated with consumption of Sauropus androgynus in Taiwan,” The Lancet, vol. 348, no. 9020, pp. 83–85, 1996.

C.-L. Wu, W.-H. Hsu, C.-D. Chiang et al., “Lung injury related to consuming Sauropus androgynus vegetable,” Journal of Toxicology—Clinical Toxicology, vol. 35, no. 3, pp. 241–248, 1997.

C.-L. Wu, W.-H. Hsu, and C.-D. Chiang, “The effect of large-dose prednisolone on patients with obstructive lung disease associated with consuming Sauropus androgynus,” Chinese Medical Journal, vol. 61, no. 1, pp. 34–38, 1998.

N. S. Wang, Y. L. Chang, and Y. T. Yao, “Fibromuscular obliteration of bronchial arteries with segmental necrosis of small bronchi following consumption of Sauropus androgynus (SA),” The FASEB Journal, vol. 11, no. 3, article A123, 1997.

J.-S. Wang, H.-H. Tseng, R.-S. Lai, H.-K. Hsu, and L.-P. Ger, “Sauropus androgynus-constrictive obliterative bronchitis/bronchiolitis—histopathological study of pneumonectomy and biopsy specimens with emphasis on the inflammatory process and disease progression,” Histopathology, vol. 37, no. 5, pp. 402–410, 2000.

M. Yamamoto, I. Higashimoto, K. Oonakahara et al., “Clinial feature of bronchiolitis obliterans associated with consumption of Sauropus androgynus,” Japanese Journal of Chest Diseases, vol. 63, no. 10, pp. 921–929, 2004.

P. T. Li, H. Chiu, J. Ma et al., “Euphorbiaceae,” in Flora of China 11, Z. Y. Wu, P. H. Rave, and D. Y. Hong, Eds., pp. 163–314, Science Press, Beijing, China, Missouri Botanical Garden Press, St. Louis, Mo, USA, 2008.

S. Soka, H. Alam, N. Boenjamin, T. W. Agustina, and M. T. Suhartono, “Effect of Sauropus androgynus leaf extracts on the expression of prolactin and oxytocin genes in lactating BALB/C Mice,” Journal of Nutrigenetics and Nutrigenomics, vol. 3, no. 1, pp. 31–36, 2010.

N. Andarwulan, D. Kurniasih, R. A. Apriady, H. Rahmat, A. V. Roto, and B. W. Bolling, “Polyphenols, carotenoids, and ascorbic acid in underutilized medicinal vegetables,” Journal of Functional Foods, vol. 4, no. 1, pp. 339–347, 2012.

N. Benjapak, P. Swatsitang, and S. Tanpanich, “Determination of antioxidant capacity and nutritive values of Pak-Wanban (Sauropus androgynus L. Merr.),” Khon-Kean University Science Journal, vol. 36, pp. 279–289, 2008.

V. Senthamarai Selvi and A. Baskar, “Evaluation of bioactive components and antioxidant activity of Sauropus androgynus plant extracts using GC-MS analysis,” International Journal of Pharmaceutical Sciences Review and Research, vol. 12, no. 2, pp. 65–67, 2012.

A. Gireesh, H. Harsha, H. Pramod, and S. D. Kholkute, “Pharmacognostic and preliminary phytochemical analysis of Sauropus androgynus (L) Merr. leaf,” International Journal of Drug Development and Research, vol. 5, no. 1, pp. 321–325, 2013.

P.-H. Wang and S.-S. Lee, “Active chemical constituents from Sauropus androgynus,” Journal of the Chinese Chemical Society, vol. 44, no. 2, pp. 145–149, 1997.

S.-F. Yu, C.-T. Shun, T.-M. Chen, and Y.-H. Chen, “3-O-β-D-gucosyl--β-D-glucosyl-kaempferol isolated from Sauropus androgynus reduces body weight gain in Wistar rats,” Biological & Pharmaceutical Bulletin, vol. 29, no. 12, pp. 2510–2513, 2006.

T. Kanchanapoom, P. Chumsri, R. Kasai, H. Otsuka, and K. Yamasaki, “Lignan and megastigmane glycosides from Sauropus androgynus,” Phytochemistry, vol. 63, no. 8, pp. 985–988, 2003.

N. Andarwulan, R. Batari, D. A. Sandrasari, B. Bolling, and H. Wijaya, “Flavonoid content and antioxidant activity of vegetables from Indonesia,” Food Chemistry, vol. 121, no. 4, pp. 1231–1235, 2010.

V. S. Selvi and A. Basker, “Phytochemical analysis and GC-MS profiling in the leaves of Sauropus androgynus (L.) MERR,” International Journal of Drug Development and Research, vol. 4, no. 1, pp. 162–167, 2012.

K. S. Sai and N. Srividya, “Blood glucose lowering effect of the leaves of Tinospora cordifolia and Sauropus androgynus in diabetic subjects,” Journal of Natural Remedies, vol. 2, no. 1, pp. 28–32, 2002.

A. Bhaskar, K. V. Ramesh, and Rajeshwari, “Wound healing profile of Sauropus androgynus in Wistar rats,” Journal of Natural Remedies, vol. 9, no. 2, pp. 159–164, 2009.

V. Senthamarai Selvi and A. Bhaskar, “Anti-inflammatory and analgesic activities of the Sauropus androgynous (L) merr. (Euphorbiaceae) plant in experimental animal models,” Der Pharmacia Lettre, vol. 4, no. 3, pp. 782–785, 2012.

K. H. Lee, A. M. Padzil, A. Syahida et al., “Evaluation of anti-inflammatory, antioxidant and antinociceptive activities of six Malaysian medicinal plants,” Journal of Medicinal Plant Research, vol. 5, no. 23, pp. 5555–5563, 2011.

S. Badami and K. P. Channabasavaraj, “In vitro antioxidant activity of thirteen medicinal plants of India's Western Ghats,” Pharmaceutical Biology, vol. 45, no. 5, pp. 392–396, 2007.

S. P. Wong, L. P. Leong, and J. H. William Koh, “Antioxidant activities of aqueous extracts of selected plants,” Food Chemistry, vol. 99, no. 4, pp. 775–783, 2006.

K. Gayathramma, K. V. Pavani, and R. Raji, “Chemical constituents and antimicrobial activities of certain plant parts of Sauropus androgynus L.,” International Journal of Pharma and Bio Sciences, vol. 3, no. 2, pp. 561–566, 2012.

V. N. Ariharan, V. N. M. Devi, and P. N. Prasad, “Antibacterial activity of Sauropus androgynus leaf extracts against some pathogenic bacteria,” International Journal of Chemical, Environmental and Pharmaceutical Research, vol. 6, no. 2, pp. 134–137, 2013.

M. Paul and K. Beena Anto, “Antibacterial activity of Sauropus androgynus (L.) Merr.,” International Journal of Plant Sciences, vol. 6, no. 1, pp. 189–192, 2011.

V. S. Selvi, G. Govindaraju, and A. Basker, “Antifungal activity and phytochemical analysis of Cympogon citratus, Sauropus androgynus and Spillanthes acmella plants,” World Journal of Fungal and Plant Biology, vol. 2, pp. 6–10, 2011.

L. Xin, X. Xi-kun, H. Jun-ming et al., “Cytotoxicity and genotoxicity of Sauropus androgynous,” Chinese Journal of Health Laboratory Technology, vol. 9, pp. 1050–1053, 2006.

S.-F. Yu, T.-M. Chen, and Y.-H. Chen, “Apoptosis and necrosis are involved in the toxicity of Sauropus androgynus in an in vitro study,” Journal of the Formosan Medical Association, vol. 106, no. 7, pp. 537–547, 2007.

X. Li, X. K. Xiong, J. M. Huang et al., “Cytotoxicity and genotoxicity of Sauropus androgynus,” Chinese Journal of Health Laboratory Technology, no. 9, 2006.

O. Yunita, M. Yuwono, and F. A. Rantam, “In vitro cytotoxicity assay of Sauropus androgynus on human mesenchymal stem cells,” Toxicological and Environmental Chemistry, vol. 95, no. 4, pp. 679–686, 2013.

M. Sawahata, T. Ogura, A. Tagawa et al., “Sauropus androgynus-associated bronchiolitis obliterans of mother and daughter—autopsy report,” Respiratory Medicine CME, vol. 3, no. 4, pp. 214–217, 2010.

H. Hsu, H. Chang, and Y. Goan, “Intermediate results in Sauropus androgynus bronchiolitis obliterans patients after single-lung transplantation,” Transplantation Proceedings, vol. 32, no. 7, pp. 2422–2423, 2000.

H. Hsu, H. Chang, J. Su, Y. Goan, C. Wong, and M. Huang, “Lung transplantation in Sauropus androgynus consumption patients in Taiwan,” Transplantation Proceedings, vol. 30, no. 7, pp. 3393–3394, 1998.

H. Sakakibara, K. Taki, M. Kawanishi, Y. Shimada, and N. Ishikawa, “Lung vascular permeability enhanced by sympathetic nerve stimulation in rats,” Japanese Journal of Pharmacology, vol. 56, no. 3, pp. 391–395, 1991.

G. U. Hung, S. C. Tsai, J. F. Hsieh, C. H. Kao, and S. J. Wang, “Detect bronchiolitis obliterans due to Sauropus androgynus vegetable ingestion: comparison with 99mTc-DTPA radioaerosol inhalation lung scintigraphy, high resolution computed tomography and pulmonary function testing,” Annals of Nuclear Medicine, vol. 13, pp. 197–202, 2000.

S.-P. Luh, Y.-C. Lee, Y.-L. Chang, H.-D. Wu, S.-H. Kuo, and S.-H. Chu, “Lung transplantation for patients with end-stage Sauropus androgynus-induced bronchiolitis obliterans (SABO) syndrome,” Clinical Transplantation, vol. 13, no. 6, pp. 496–503, 1999.

Y.-L. Chang, J.-S. Chen, H.-D. Wu, and Y.-C. Lee, “Retransplantation of contralateral lung in a patient with Sauropus androgynus-induced bronchobronchiolitis obliterans,” Transplantation Proceedings, vol. 32, no. 7, pp. 2432–2434, 2000.

J. Svetlecic, A. Molteni, and B. Herndon, “Bronchiolitis obliterans induced by intratracheal papaverine: a novel animal model,” Lung, vol. 182, no. 2, pp. 119–134, 2004.

T.-J. Lin, C.-C. Lu, K.-W. Chen, and J.-F. Deng, “Outbreak of obstructive ventilatory impairment associated with consumption of Sauropus androgynus vegetable,” Journal of Toxicology—Clinical Toxicology, vol. 34, no. 1, pp. 1–8, 1996.

V. Cottin and J.-F. Cordier, “Bronchiolitis,” in Diffuse Lung Disease: A Practical Approach, pp. 343–363, Springer, 2nd edition, 2013.

A. El-Gamel, E. Sim, P. Hasleton et al., “Transforming growth factor beta (TGF-β) and obliterative bronchiolitis following pulmonary transplantation,” Journal of Heart and Lung Transplantation, vol. 18, no. 9, pp. 828–837, 1999.

H. M. Romanska, T. S. Ikonen, A. E. Bishop, R. E. Morris, and J. M. Polak, “Up-regulation of inducible nitric oxide synthase in fibroblasts parallels the onset and progression of fibrosis in an experimental model of post-transplant obliterative airway disease,” Journal of Pathology, vol. 191, no. 1, pp. 71–77, 2000.

A. M. Stevens, A Comprehensive Indonesian-English Dictionary, Penerbit Mizan Bandung, Bandung, Indonesia, 2004.

H. C. Ong, Sayuran: Khasiat Makanan & Ubatan, Utusan Publications and Distributors, Kuala Lumpur, Malaysia, 2003.

N. Arifin, Penyembuhan Semula Jadi Dengan Herba, PTS Litera Utama, Kuala Lumpur, Malaysia, 2005.

Y. R. Chadha, The Wealth of India, Publication and Information Directorate, New Delhi, India, 1972.

Y. Liu, C. O. Perera, and V. Suresh, “Comparison of three chosen vegetables with others from South East Asia for their lutein and zeaxanthin content,” Food Chemistry, vol. 101, no. 4, pp. 1533–1539, 2007.