Siddiqui Z. Khan M. I, Badruddeen B, Akhtar J, Ahmad M. Multifunctional Role of Phyllanthus Acidus L. As a Therapeutic Agent for Management of Diabetes and Associated Complications: A Review. Biomed Pharmacol J 2022;15(4).

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Manuscript received on :21-06-2022
Manuscript accepted on :06-10-2022
Published online on: 03-11-2022

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Zeba Siddiqui, Mohammad Irfan Khan^*, Badruddeen, Juber Akhtar, Mohammad. Ahmad

Department of Pharmacognosy, Faculty of Pharmacy, Integral University, Dasauli Kursi Road Lucknow, India.

Corresponding Author E-mail: irfanrndgp@gmail.com

DOI : https://dx.doi.org/10.13005/bpj/2520

Abstract

Background: Plant based medicines have been used in traditional system of medicines since time immemorial for the treatment of diabetes due to relatively low prevalence of side effects and ease of access in developing countries. Objective: The review compiles and analyses the scientific data to accentuate the role of Phyllanthus acidus also known as star gooseberry, as a promising treatment for the management of diabetes and related complications. Method: Several electronic databases like Google Scholar, Pub Med, Scopus, Web of Science, Science Direct etc. and other published data in books and dissertations were utilised to compile this review. Result: Both in-vitro and in-vivo research have indicated that the phytoconstituents present in Phyllanthus acidus may affect the various biomarkers of diabetes. The mode of action behind antidiabetic property of the plant and its biologically active components are mainly due to inhibition of 𝛼-glucosidase, suppression of PPAR-𝛾, and elevate production of insulin. Conclusion: The antioxidant and anti-inflammatory studies pertaining to Phyllanthus acidus also strengthen its claim as an effective antidiabetic agent. Therefore, Phyllanthus acidus shows promising therapeutic potential to be used in the treatment of diabetes and its co morbidities.

Keywords

Antidiabetic; 𝛼-glucosidase; Antioxidant; Anti-inflammatory;  Insulin secretion

Introduction

Diabetes mellitus a metabolic disorder is one of the major challenges faced by the healthcare industry globally and a major economical and medical burden to the patient. India being home to about 74 million diabetics is considered as the “diabetic capital” sharing a major part of the global burden of diabetes.¹ According to Global Burden of Disease the various micro and macro vascular complications associated with diabetes are retinopathy (moderated to severe low vision and blindness), diabetic neuropathy, amputations resulting from diabetic foot and cardiovascular disorders.² Linked with chronic hyperglycemia diabetes is usually classified into Type I, Type II and gestational diabetes. Occurrence of Type I diabetes happens when the beta cells present in pancreas are damaged and not able to produce insulin in sufficient quantity to maintain blood glucose levels.³ In this case the patients are entirely dependent on exogenous insulin administration to maintain the blood glucose levels. On the contrary Type II diabetes which is observed in majority of the patients is due to peripheral insulin resistance resulting in diminished insulin sensitivity to skeletal muscle, liver and adipose tissues. Pregnant women who had not been earlier diagnosed with diabetes often suffer from gestational diabetes.⁴ There are various conventional antidiabetic medications available for the treatment and management of diabetes via exogenous supply of insulin, enhancing insulin sensitivity and secretion and stimulating glucose uptake. However, prolong use of these medication may lead to adverse events like hepatic failure, diarrhoea, weight gain, lactic acidosis, tachycardia and hypothyroidism.⁵ This has lead to an increase in demand of efficient and affordable alternatives with lesser side effects.

Traditional medicine has been used for the management of diabetes and its complication in various ethnic cultures like Indian, Chinese, Mexican and Korean for thousands of years. The popularity of these herbal drugs is increasing due to comparatively lower cost, greater patience forbearance, lower adverse events at prescribed dosages, and overall acceptance due to well established historical usage. There is a renewed interest in plant-based pharmaceuticals and lead molecules as alternative medicament for diabetes. Researchers are delving into areas like medicinal chemistry, ethnoparmacology, and clinical trials of these traditional medicines validating their clinical usage.⁶ Plants comprising of phenolic compound have been found to reduce the risk of cancer, diabetes, inflammation, and viral diseases.⁷ This property of plants comprising of phenols may be attributed to the free radical scavenging, lowering oxidative stress, and antioxidant property of polyphenolic constituents. In case of diabetes and related complications these compounds have been found to modulate lipid and carbohydrate metabolism by obstructing the effect of digestive enzymes where by reducing postparandial hyperglycemia and dyslipidemia. Polyphenolic compounds have been instrumental in diminishing insulin resistance, ameliorating pancreatic beta-cell function by safeguarding them against oxidative damage and invigorating their insulin.⁸

The present review intents to compile scientific investigations pertaining to phytoconstituents and pharmacological studies, supporting the development of drugs, foods and alternate therapies for management of diabetes and related disorders to combat this global pandemic. Phyllanthus acidus is an ornamental plant with a long history of culinary and folklore use. Also known as Tahitian gooseberry, Star gooseberry, Malay gooseberry, Otaheite gooseberry, country gooseberry, arbari, West India gooseberry, or simply gooseberry tree has yellow greenish edible berry fruits. The fruits are acidic sour and tart in taste. The plant that is said to have originated in Madagascar is mainly found in the Indian subcontinent and Malay Peninsula.^{9, 10} It has been utilized in various conventional system of medicine for therapeutics of diabetes and other diseases. The aim of this review is to advocate the use of this plant in future scientific investigations and clinical studies and to unlock its true potential as an alternative or complimentary treatment for diabetes.

Material and Methods

Several electronic databases like Google Scholar, Pub Med, Scopus, Web of Science, Science Direct etc. and other published data in books and dissertations were utilised to compile this review. Literature based search, covering reports that have been published regarding the phytochemical, pharmacological and toxicity studies of P.acidus was carried out. Emphasis was given to article covering various aspects of antidiabetic potential of P.acidus. The search strategy included the use of MESH terms and keywords such as Phyllanthus acidus, Diabetes, NIDDM, T2D, Hyperglycemia, 𝛼-glucosidase inhibition, insulin secretagouges, antioxidant, anti-inflammatory, toxicity to search various databases. Studies that were in English language and whose full text were available and reported the relevent in-vivo and in-vitro studies of antidiabetic, antioxidant, and anti-inflammatory activity of Phyllanthus acidus were selected. Exclusion criteria included non-English studies, data for diabetes that could not be separated from other pharmacological activities, and non availability of full-text articles.  On the basis of these keywords 110 articles were identified, abstracts of 100 articles were screened and 85 full text articles were scrutinised for eligibility and of these 71 original articles were included in this literature review.

Ethnomedicine

 Prior to examining the scientific evidence pertaining to antidiabetic effect and related activities, it is requisite that we briefly delve into the ethnomedicinal utilization of this herb to prove its historical application. The fruit of Phyllanthus acidus is somewhat bitter, aromatic, pungent, and sour and enhances appetite. In Ayurveda it is useful for the treatment of bronchitis, biliousness, urinary concentrations, and piles. It also increases “Vata”in Ayurvedic practices.⁹ The fruit is used to enrich the blood and as liver tonic and blood purifier.¹¹ Latex is said to possess emetic and laxative effect. Coconut oil heated with bark is applied on cracks on hands and feet in Indonesia to treat eruptions. Roots are used as medication for psoriasis.¹² The root extract is utilized to manage asthma, relieving cough, and headache.¹⁰ In the Philippines, leaf decoction is utilized for the treatment of urticaria while bark is used to cure catarrh .¹³ Mucilaginous nature of the leaves makes it useful as demulcent in case of treatment of gonorrhoea.¹⁰ The bark has limited use as a tanning agent in India. The tough and durable nature of the wood makes it suitable for making dishes and other items.¹⁴ The culinary use of the sour mature fruits is widespread. It is eaten fresh and used in cooking for flavour. The fruit is used as chutneys, pickles and jams. The fruit juice serves as make cold drinks while fruit is used for manufacturing vinegar. The young leaves are used as vegetables in India, Thailand, and Indonesia.¹⁵ The fruit is also used to treat diabetes, relieve cough, and enhance memory.¹⁶

Phytochemistry

 Preliminary analyses of fruits of P.acidus showed that it mostly consist of water, glucose, and fructose. It was also rich in ascorbic acid, carotenoids and macro and micro nutrients like calcium, magnesium and iron making it a good candidate for dietary supplements.^{17, 18} The review of the literature showed that the plant mainly contains phytoconstituents like terpenoid, flavonoids, natural nucleosides, phenolic compounds, and volatile oil components as shown in Table 1.

Table 1: Phytochemical constituents of different parts of P. acidus

Anti-diabetic effects of star gooseberry

The bioactive components of star gooseberry (Phyllanthus acidus) have shown to exhibit antioxidant, anti-inflammatory, hepatoprotective, hypoglycaemic, antimicrobial, and cytotoxic properties (Table 2).The evidence provided by these studies indicated that P.acidus can modulate molecular mechanisms by affecting transcription factors and different intracellular pathways. This review primarily focuses on the potent antidiabetic potential of this plant. Enhancing the glycemic profile by the star gooseberry bioactive components can control the complications due to diabetes. Figure 1

Figure 1: Mechanisms of action of Antidiabetic property of Phyllanthus acidus. Click here to view figure

Table 2: Therapeutic properties of P. acidus

In-vivo hypoglycaemic studies

Various studies have reinforced the affirmation about the ethnomedical application of P.acidus for the management of diabetes and related disorders.¹⁶ Extracts of P.acidus plant as a whole have shown hypoglycaemic or antidiabetic properties.

Hypoglycaemic activity of etanolic leaf extract of P.acidus was demonstrated by employing glucose oxidase procedure, where doses of 200mg/kg p.o and 100mg/kg p.o reduced glucose level after two hours in albino rat. Where, the reduction was found to be more significant for 200mg/kg when compared with standard drug glibenclamide 0.5mg/kg p.o.³⁵ Furthermore the extracts from Phyllanthus acidus (L.), Leucaena leucocephala (Lam.) and Psidium guajava (L.) leaves were found to have considerable hypoglycaemic and hypolipidimic activity and may be utilized as therapeutics for diabetes without compromising  haematological standards or kidney functioning.³⁶ This property may be attributed to hyper insulinemia and antioxidant activity of extracts. The fruit pulp methanolic extract of P.acidus showed significant hypoglycaemic activity. The extract also showed effective antidiarrheal property and subdued the rate of excretion by 54.24%.³⁷ The extract also showed considerable analgesic and CNS anaesthetic activity on experimental animals. P.acidus seed extract at a dose of 200mg/kg exhibited decline in blood glucose level after 8 and 12 hours of treatment. When compared with glibenclamide as standard.³⁸

Insulin Secretagogues

 Koyoto declaration of 2013 emphasised the importance of insulin secretagouges as treatment for diabetes in Asia, as well as worldwide. The statistical data indicated a distressing need for significant clinical and intrinsic research on diabetes in the Asian region. It was stipulated that the Asian phenotype of diabetes was different than that of other geographical regions as it was mostly non obese  and insulin secretory dysfunction rather than the more common type which was obesity and insulin resistance diabetes usually found around the world ³⁹. The leaf extract of P.acidus showed significant hypoglycaemic effects by inducing division of beta cell leading to insulin production in streptozotocin induced diabetic rats.⁴⁰ Plant extract at a dose of 250mg/kg was found to be slightly less than that of glibenclamide. Furthermore it was surmised that alcoholic extract of P.acidus leaves was at a lesser dose nearly non toxic as the animals endured up to 2000mg/kg of orally administered dose of the extract. Etanolic extract of P.acidus was effective in gradually decreasing the blood glucose levels of experimental animals.⁴¹ Histopathological studies indicated an increase number of beta cells and normalising effect on other factors like body weight, creatine kinase, glycosylated haemoglobin, and lactate dehydrogenase affirming the role of this plant for glycemic control.⁴²

a-Glucosidase Inhibitory Activities

 Moderation of blood glucose can also be achieved by inhibition of carbohydrate- digesting enzymes such as a-Glucosidase resulting in malabsorption of monosaccharides thus reducing insulin elevation.⁴³ The inhibition this enzyme has been found useful for the therapeutics of type 2 diabetic patients.⁴⁴ The most widely used synthetic starch hydrolase inhibitors are acarbose, miglitol, and voglibose and have been used as an antidiabetic compounds. However, various adverse events are associated with use of synthetic inhibitors like hypoglycaemia at elevated doses, flatulence because of fermentation of intestinal microflora on undigested sugars and diarrhoea.⁴⁵ This has led to exploration of natural a–glucosidase inhibitors, a facet under which compounds of P.acidus have been explored as well.

Phenolic compounds present in fruit extract of P.acidus were analysed using Ultra-high performance liquid chromatography. The fruit extract showed significant a-glucosidase inhibitory activity which may be attributed to phenolic and flavanoidal components like gallic acid, myricetin, quercetin, kaempferol, and dihydroquercetin when compared with forty extracts from tropical fruits from Malaysia.⁴⁶ Derivatives of kaempferol, epicathechin, coumarin and cinnamic acid along with quercetin, citric acid, feruloylacetic acid, 4-amino-3-hydroxybutyrate, mucic acid, 2”-O-feruloylorientin, diphylloside B, phyllanthusiin E and peonidin-3-glucoside were elucidated from 50% ethanolic extract that ascribed to the a-glucosidase inhibitory activity.⁴⁷

PPAR-g Agonistic Activity

 In the previous decade or so a subfamily of nuclear receptors have emerged as worthy pharmacological receptors whose invigoration can modulate the metabolic disorders and diminish cardiovascular threat factors linked with type 2 diabetes.⁴⁸ Thiazolidinediones a synthetic PPAR-γ agonist is an insulin stimulator that rescinds lipotoxicity catalysed insulin resistance in diabetic patients.⁴⁹ Nevertheless, like many of the side effects associated with synthetic drugs and an epidemic increase of type 2 diabetes, there is a dire need for novel and safer PPAR-γ agonist with better efficacy and safety. Screening of medicinal plants for PPAR- γ agonist activity seems a logical strategy for finding antidiabetic drugs. After extensive search no investigation into this aspect of diabetes control for this plant could be found. Thus, suggesting an aspect of antidiabetic effect of P.acidus plant as PPAR-γ agonist to be explored as possible mechanism of action.

Other Pharmacological Properties of P.acidus associated with Diabetes

  Production of inflammatory mediators due to oxidative stress results in generation of reactive oxygen species. This link between oxidative stress, inflammation, and diabetes is important for the study of therapeutics of diabetes.⁵⁰ Plants comprising of phenolic and flavonoidal constituents have been found to reduce the risk of cancer, diabetes, inflammation and viral diseases. This property of plants comprising of phenols and flavonoids may be attributed to the free radical scavenging, lowering oxidative stress and antioxidant activity of these polyphenolic compounds.⁵¹ Occurrence of oxidative stress due to persistent hyperglycemia is one of the causes of onset of diabetes and its complications. Mechanisms that are responsible for increased oxidative stress are metabolic stress, auto-oxidation of glucose and increased non-enzymatic glycosylation of glucose.⁵² P.acidus is rich in terpenoids, phenols and flavonoids like gallic acid, rutin, quercetinls, myricetin etc. and possesses antioxidant activity due to the presence of hydroxyl groups which help in scavenging of free radicals.⁵³Inhibition of antioxidant enzymes caused by elevated free radicals is reduced resulting in antioxidant activity. This further leads to reduction of lipid peroxidation in tissues.⁵⁴As it is evident that Type II diabetes mellitus is an inflammatory disease that leads to increase in the presence of cytokines and oxidative stress related to them, resulting in an increase in the stress activated signalling pathways. The entire process initiates insulin resistance and decreased glucose tolerance in humans.⁵⁵ Presence of compounds like flavonoids, kaempferol, and quercetin in P.acidus was responsible for the scavenging of Nitric Oxide (NO) and superoxide anions responsible for inflammatory response. Furthermore P.acidus  also attenuated the expression of inflammatory markers like IL-1β.⁶¹Therefore the anti-inflammatory and antioxidant effect of P.acidus is examined here, regarding the prospective use P.acidus in diminishing the damaging consequences due hyperglycemia related oxidative stress and inflammation.

Antioxidant Activity of P. acidus

 The in-vivo scavenging activity of free radicals by various extract of bark, roots, leaves, and fruit of P.acidus against superoxides, DPPH, hydroxyl radicals etc. is used to evaluate its antioxidant property.  NO scavenging activity was observed in 50% ethanolic extract of leaf of P.acidus.⁴⁷ The methanolic extract of fruits of P.acidus was found to possess antioxidant activity owing to the various phenolic compounds found in it.⁵⁶ Due to higher phenolic content ethanolic extract of bark showed remarkable antioxidant activity. The extract showed ABTS radical scavenging at 90% at dose of 50µg/mL. Investigation of the methanolic extract also revealed the presence of prominent antioxidant compounds like quercetin, gallic acid, rutin, , myrcetin, luteolin, coumaric acid, and hydroxyl benzoic acid.⁴² The leaf and fruit of P.acidus were found to check oxidative damage induced due to free radical. This can be utilized to treat cardiovascular and inflammatory disease.⁵⁷ The alcoholic and aqueous extracts of P.acidus fruits were evaluated for their antioxidant and cytotoxic activity. The study also showed that aqueous extract exhibited more potent pharmacological effect than ethanolic extract.⁵⁸

Anti-inflammatory Activity of P. acidus

The P.acidus leaf extract exhibited notable anti-inflammatory and analgesic action.⁵⁹ The etanolic extract of the leaves also exhibited notable anti-inflammatory and anti-nociceptive property due to high flavanoid and phenolic compounds and can be considered as a medicine against pain, oxidative stress, and inflammatory diseases ⁶⁰. Aqueous extract of P.acidus fruit was utilized for silver nanoparticles (AgNP) green synthesis from aqueous AgNO3.⁶¹ These characterized AgNP showed remarkable anti-inflammmatory activity through scavenging nitric oxide and super oxide anions. The AgNP’s did not offset the viability of peritoneal macrophages and can be utilized for the therapeutics of inflammatory diseases by attenuating the expression of IL-1β.⁶¹ Methanolic extract of P.acidus showed both in vivo and in vitro anti-inflammatory activity. The orally administered extract also restored the HCl/ethanol- instigated gastric damage and acetic acid vascular permeability. The compounds identified were flavonoids, kaempferol and quercetin.⁶²

Toxicity Studies

Limited literature exists relating to the toxicity studies of P.acidus. Although considered toxic in Malay few citations are available regarding the toxicity studies of this plant. The safety profile of ethanolic extract of P.acidus leaves was established through subchronic toxicity assay.⁶³ The outcome showed that not only the extract could reduce the body weight as compared to the control group but all the other haematological parameters after administration of the extract were similar to that of control group. There was no change in the levels of alanine aminotransferase, glucose, blood urea nitrogen levels but an elevated aminotransferase, creatinine and urine volume. The examination of the various organs showed that though the organ/body weight ratios of heart and liver were unaltered at all doses however the liver was enlarged and kidney shrunken. The result indicated that the extract was relatively safe at subchronic doses but at higher doses the liver and kidney need to be critically monitored .In an earlier study to establish the antiplasmodial activity of the various extracts of P.acidus it was found that extracts were non-toxic up to concentration of 50µg/ml when tested for cytotoxicity on Vero normal cell lines.⁶⁴

Conclusions

The various evidence collected from the scientific publications establishes the worthiness of P.acidus, to be investigated and advocated as complementary or alternate therapy for management of diabetes and its complications. More in-depth studies are required to determine the phytoconstituents responsible for hypoglycaemic activity of this plant. The aspect of insulin resistance, a major characteristic of type 2 diabetes and the ability of P.acidus to combat it need to be evaluated. Genetically altered rat models like Goto-Kakizaki model can be utilized to determine the insulin resistance in type 2 diabetes. Another aspect which needs to be explored is the isolation of bioactive constituents responsible for pancreatic regeneration of the β cell utilizing both in vitro and in-vivo studies. However in comparison to the plants employed in conventional system of therapeutics for mitigation of diabetes, P.acidus has progressed credibly in terms of research based evaluations including pharmacognostic appraisal of raw drug ,isolation of bioactive components, and exploring the mechanism of therapeutic activities. Although the use of P.acidus may be advocated for treatment of hyperglycemia, its use for the purpose of overall health and wellbeing should also be encouraged. In spite of plethora of research available on P.acidus it is imperative that pharmacological and toxicological facet of the plant are also studied through in-vivo and clinical studies. There is also a need to determine the recommended dosage and intake limit prior to its utilization as antidiabetic agent.

Acknowledgement

The authors are thankful to Faculty of Pharmacy, Integral University for providing the necessary resources for the compilation of this article.

Conflicts of Interests

The authors declare that they do not have any Conflicts of Interests.

Funding Sources

This study received no external funding. 

References

1. Pradeepa R., Mohan V. Epidemiology of type 2 diabetes in India. Indian J Ophthalmol. 2021;69(11):2932-2938
2. Deshpande A.D., Harris-Hayes M., Schootman M. Epidemiology of diabetes and diabetes-related complications. Phys Ther. 2008 ;88(11):1254-64
3. Galicia-Garcia U., Benito-Vicente A., Jebari S., Larrea-Sebal A., Siddiqi H., Uribe K.B., Ostolaza H., Martín C. Pathophysiology of Type 2 Diabetes Mellitus. Int J Mol Sci. 2020;21(17):6275
4. Choudhury H., Pandey M., Hua C.K., Mun C.S., Jing J.K., Kong L., Ern L.Y., Ashraf N.A., Kit S.W., Yee T.S., Pichika M.R., Gorain B., Kesharwani P. An update on natural compounds in the remedy of diabetes mellitus: A systematic review. J Tradit Complement Med. 2017; 8(3):361-376.
5. Li G.Q., Kam A., Wong K.H., Zhou X., Omar E.A., Alqahtani A., Li K.M., Razmovski-Naumovski V., Chan K. Herbal medicines for the management of diabetes. Adv Exp Med Biol. 2012; 771:396-413.
6. Pamunuwa G., Karunaratne D.N., Waisundara V.Y. Antidiabetic Properties, Bioactive Constituents, and Other Therapeutic Effects of Scoparia dulcis. Evid Based Complement Alternat Med. 2016; 8243215. doi: 10.1155/2016/8243215.
7. Shahidi, F, and Ambigaipalan, P. Phenolics and polyphenolics in foods, beverages and spices: Antioxidant activity and health effects – A review. Journal of Functional Foods.2015; 18: 820–897. https://doi.org/10.1016/J.JFF.2015.06.018.
8. Peixoto Araujo N.M, Arruda H.S, de Paulo Farias D, Molina G, Pereira G.A, Pastore G.M. Plants from the genus Eugenia as promising therapeutic agents for the management of diabetes mellitus: A review. Food Res Int.2021; 142:110182.
9. Kirtikar K.R, Basu B.D. Indian medicinal plants. Lalit Mohan Basu Allahabad. 1935: 2227.
10. Morton F.J. Otaheite Gooseberry In: Fruits of warm climate. Miami FL. 1987: 217
11. Hazarika R, Abujam S.S, Neog B. Ethno Medicinal Studies of Common Plants of Assam and Manipur. International Journal of Pharmaceutical & Biological Archives. 2012;3(4):809
12. Brooks R, Barnaby A.G, Bailey D. Nutritional and Medicinal Properties of Phyllanthus Acidus (Jimbilin), International Journal of Fruit Science. 2020; 20(3): S1706-S1710
13. Lemmens R.H., Bunyapraphatsara M.I., De Padua L.S. Plant resources of south-East Asia. Medicinal and poisonous plants I. Prosea Foundation, Bogor, Indonesia. 1999;12(1):386
14. Rizk A.F.M. The chemical constituents and economic plants of Euphorbiaceae. Botanical Journal of the Linnean Society. 1987;94(1): 293
15. Prasad D. Edible fruits and vegetables of the English speaking Caribbean. Caribbean Food and Nutrition Institute, Kingston, Jamaica. 1986:75
16. Unander D.W., Webster D.W., Blumberg B.S. Uses and bioassays in Phyllanthus (Euphobiaceae): a compilation I. Subgenera Isocladus, Kirganelia, Cicca and Emblica. Ethnopharmacol. 1991; 30:233-264.
17. Rahman S.M.M., Mosihuzzaman M.Free sugars and dietary fibre in some fruits of Bangladesh. Food Chem. 1991. 42:19
18. Shajib M.T.I., Kawser M., Miah M.N., Begum P., Bhattacharjee L., Hossain A., Fomsgaard I.S., Islam S.N. Nutritional composition of minor indigenous fruits: Cheapest nutritional source for the rural people of Bangladesh. Food Chem. 140:466
19. Vongvanich N., Kittakoop P., Kramyu J., Tanticharoen M., Thebtaranonth Y. Phyllanthusols A and B, cytotoxic norbisabolane glycosides from Phyllanthus acidus The Journal of Organic Chemistry. 2000; 25: 5420-5423.
20. Durham D.G., Reid R.G., Wangboonskul J., Daodee S. Extraction of Phyllanthusols A and B from Phyllanthus acidus and analysis by capillary electrophoresis. Phytochem. Analysis. 2002; 13:358-362.
21. Duong T.H., Bui X.H., Pogam P.L., Nguyen H.H., Tran T.T., Nguyen T.A.T., Chavasiri W., Boustie J., Nguyen K.P.P. Two novel diterpenes from the roots of Phyllanthus acidus (L.) Skeel . Tetrahedron. 2017; 73: 5634-5638.
22. Duong H., Nguyen H., Nguyen T., Bui H. Triterpenoids from Phyllanthus acidus (L.) Science and Technology Development. Journal – Natural Sciences. 2019; 2(2): 71.
23. Ultee A.J. Pharm. Weekbl. 1933; 70: 1173–1175.
24. Sengupta P., Mukhopadhyay J. Terpenoids and related compounds-VII: Triterpenoids of Phyllanthus acidus Phytochemistry.1966; 5: 531-534.
25. Lv J.J., Yu S., Wang Y.F., Wang, D., Zhu H.T., Cheng R.R., Yang C.R., Xu M., Zhang Y.J. Anti-Hepatitis B Virus Norbisabolane Sesquiterpenoids from Phyllanthus acidusand the Establishment of Their Absolute Configurations Using Theoretical Calculations. Org. Chem. 2014; 79(12), 5432-5447.
26. Gu C., Yin A.P., Yuan H.Y., Yang K., Luo J., Zhan Y.J., Yang C.R., Zuo D.M., Li H.Z., Xu M. New anti-HBV norbisabolane sesquiterpenes from Phyllantus Fitoterapia. 2019; 137: 104151.
27. Zheng X.H., Yang J., Lv J.J., Zhu H.T.,Wang D., Xu M., Yang C.R., Zhang Y.J. Phyllaciduloids A–D: Four new cleistanthane diterpenoids from Phyllanthus acidus (L.) Skeels. Fitoterapia. 2018; 125:89-93.
28. Tram N.C.T., Son N.T., Nga N.T., Phuong V.T.T., Cuc N.T., Phuong D.T., Truan G., Cuong N.M., Thao D.T. Kaempferol and kaempferol glycosides from Phyllanthus acidus Med Chem Res.2017; 26: 2057–2064.
29. Geng H.C., Zhu H.T., Yang W.N., Wang D., Yang C.R., Zhang Y.J. New cytotoxic dichapetalins in the leaves of Phyllanthus acidus: Identification, quantitative analysis, and preliminary toxicity assessment. Bioorganic Chemistry. 2021; 114: 105125.
30. Duong T.H., Trung N.T., Phan C.T.D., Nguyen V.D., Nguyen H.C., Dao T.B.N., Mai D.T., Niamnont N., Tran T.N.M., Sichaem J. A new diterpenoid from the leaves of Phyllanthus acidus, Natural Product Research. 2020 ; 36(2) : 539-545
31. Khatun M., Billah M., Quader Md.,A. Sterols and sterol glucoside from Phyllanthus Species. Dhaka Univ. J. Sci. 2012; 60: 5-10.
32. Colmenares A.P., Díaza Y.O., Fermín L.R., Zambrano R.A., Arzola J.C., Usubillaga A. Chemical Composition of the Essential Oil of Phyllanthus acidus. Natural Product Communication. 2018; 13(1), 97-98.
33. Pino J., Cuevas L., Marbot R., Fuentes V. Volatile compounds of grosella (Phyllanthus acidus [L.] Skeels) fruit. Revista CENIC Ciencias Químicas. 2008;39: 3-5
34. Xin Y., Xu M., Wang Y.F., Zheng X.H., Zhu H.T., Wang D., Yang C.R., Zhang Y.J. Phyllanthacidoid U: a new N-glycosyl norbisabolane sesquiterpene from Phyllanthus acidus (L.) skeels, Natural Product Research.2021;35(21): 3540-3547
35. Bhowmik A., Sarkar K., Ghosh R., Das L. Hepatoprotective and hypoglycaemic activity of Phyllanthus acidus leaf extract in Wister albino rats. J. Pharm. Biol. Sc. 2015; 4: 9-16.
36. Talubmook C., Buddhakala N. Hypoglycemic and Hypolipidemic Properties of Leaf Extracts from Phyllanthus acidus (L.)Skeels., Leucaena leucocephala (Lam.) de Wit. and Psidium guajava (L.) in Streptozotocin- Induced Diabetic Rats. GSTF International Journal of BioSciences. 2013; 2(2):31-34
37. Afrin F., Banik S., Hossain S.M. Pharmacological activities of methanol extract of Phyllanthus acidus Journal of Medicinal Plants Research. 2016;10(43),790-795
38. Chigurupati S. Antioxidant and antidiabetic properties of Phyllanthus acidus (L.) Skeels ethanolic seed extract. Food Research Journal. 2020; 27(4):775-782
39. Asian Association for the Study of Diabetes. Promoting research for better diabetes care in Asia: Kyoto declaration on diabetes. J Diabetes Investig. 2013; 4(2):222.
40. Chainum-aom N., Chomko S., Talubmook C. Effects of Phyllanthus acidus Leaf Extract on Hypoglycemic Activity in Normal and Diabetic Rats. ARPN Journal of Science and Technology. 2016;6(4):110-113
41. Chaimum-aom N., Chomko S., Talubmook C. Toxicology and oral glucose tolerance test (OGTT) of Thai medicinal plant used for diaibetes control, Phyllanthus acidus (Euphobiaceae). Pharmacogn. J. 2017; 9: 58-61.
42. Shilali K., Ramachandra Y.L., Rajesh K.P., Kumara Swamy B.E. Assessing the Antioxidant Potential of Phyllanthus acidus Bark Extracts. J. Pharma. Sci. 2014; 6: 522-531.
43. Delorme S., Chiasson J.L. Acarbose in the prevention of cardiovascular disease in subjects with impaired glucose tolerance and type 2 diabetes mellitus. Current Opinion in Pharmacology. 2005;5(2): 184–189
44. Laar van de F.A., Lucassen P.A., Akkermans R.P., van de Lisdonk E.H., Rutten G.E., van Weel C. a-Glucosidase inhibitors for patients with type 2 diabetes: results from a Cochrane systematic review and meta-analysis. Diabetes Care. 2005;28(1):154–163
45. Lee W.K., Wong L.L., Loo Y.Y.,  Kasapis S., Huang D. Evaluation of different teas against starch digestibility by mammalian glycosidases. Journal of Agricultural and Food Chemistry. 2010;58(1):148–154
46. Sulaiman S.F., Ooi K.L. Antioxidant and α-glucosidase inhibitory activities of 40 tropical juices from Malaysia and identification of phenolics from the bioactive fruit juices of Barringtonia racemosa and Phyllanthus acidus. Agric. Food Chem. 2014; 62: 9576-9585.
47. Abd Ghafar S.Z., Mediani A., Ramli N.S., Abas F. Antioxidant, α-glucosidase, and nitric oxide inhibitory activities of Phyllanthus acidus and LC–MS/MS profile of the active extract. Food Biosci. 2018; 25:134-140.
48. Botta M., Audano M., Sahebkar A., Sirtori C.R., Mitro N., Ruscica M. PPAR Agonists and Metabolic Syndrome: An Established Role? International Journal of Molecular Sciences. 2018; 19(4):1197
49. Gross B., Staels B. PPAR agonists: multimodal drugs for the treatment of type-2 diabetes. Best Practice & Research Clinical Endocrinology and Metabolism. 2007; 21(4): 687-710.
50. Oguntibeju O.O. Type 2 diabetes mellitus, oxidative stress and inflammation: examining the links. Int J Physiol Pathophysiol Pharmacol. 2019;11(3):45-63
51. Kukić J., Petrović S., Niketić M. Antioxidant activity of four endemic Stachystaxa. Biol. Pharm. Bull. 2006; 29: 725–729.
52. Schultz A., Johansen J., Harris A. K., Rychly D. J., Ergul A. Oxidative stress and the use of antioxidants in diabetes: Linking basic science to clinical practice. Cardiovascular Diabetology. 2005; 4(5): 1–11.
53. Chandra K., Khan W., Jetley S., Ahmad S., Jain S. Antidiabetic, toxicological, and metabolomic profiling of aqueous extract of Cichorium intybus seeds. Pharmacognosy Magazine. 2018; 14(57): 377.
54. Brewer M. S. Natural antioxidants: Sources, compounds, mechanisms of action, and potential applications. Comprehensive Reviews in Food Science and Food Safety. 2011; 10(4): 221–247.
55. Evans J. L., Goldfine I. D., Maddux B. A., Grodsky G. M. Oxidative stress and stress-activated signaling pathways: A unifying hypothesis of type 2 diabetes. Endocrine Reviews. 2002; 23(5): 599–622.
56. Pradeep C.K., Sunikumar C.R., Swati K., Basavaraj G.L., Madhusudhan M.C., Udayashankar A. C. Evaluation of in vitro antioxidant potential of Phyllanthus acidus fruit. Res. J. Life Sc. Bioinfo. Pharma. Chem. Sc. 2018; 4(6): 30–41.
57. Angamuthu J., Ganapathy M., Evangeline V.K. Evaluation of antioxidant activity of Phyllanthus acidus. World Journal of Pharmacy and Pharmaceutical Sciences. 2016;5(10): 1011-101
58. Andrianto D., Widianti W., Bintang M. Antioxidant and Cytotoxic Activity of Phyllanthus acidus Fruit Extracts. IOP Conf. Ser.: Earth Environ. Sci. 2017;58(01): 2022

59. Hossain M.S., Akter S., Begum Y., Bulbul J.I. Analgesic and Anti-inflammatory Activities of Ethanolic Leaf Extract of Phyllanthus acidus on Swiss Albino Mice. European Journal of Medicinal Plants. 2016;13(1):1-10
60. Chakraborty R., De B., Devanna N., Sen S. Antiflammatory, antinoceptive and antioxidant activities of Phyllanthus acidus extracts. Asian Pac. J. Trop. BioMed. 2. 2012: S953–S961.
61. Manikandan R., Beulaja M., Thiagarajan R., Palanisamy S., Goutham G., Koodalingam A., Prabhu N.M., Kannapiran E., Jothi Basu M., Arulvasu C., Arumugam M. Biosynthesis of silver nanoparticles using aqueous extract of Phyllanthus acidus fruits and characterization of its anti-inflammatory effect against H₂O₂ exposed rat peritoneal macrophages. Process Biochemistry. 2017;55, 172-181
62. HossenJ., Jeon S.H., Kim S.C., Kim J.H., Jeong D., Sung N.Y., Yang S., Baek K.S., Kim J.H., Yoon D.H., Song W.O., Yoon K.D., Cho S.H., Lee S., Kim J.H., Cho J.Y. In vitro and in vivo anti-inflammatory activity of Phyllanthus acidus methanolic extract. Journal of Ethnopharmacology. 2015;168:217-228
63. Bambang S.A., Yulinah S.E., Soraya R., Atyani H., Luthfina M., Suryani, Nar V.S. Sub chronic toxicity studies of Phyllanthus acidus (Skeels)leaves extract in experimental animals. Medicinal Plants- Int. J. of Phytomedicine and Related Industries. 2019;11(3):237
64. Bagavan A., Rahuman A., Kamaraj C., Kaushik N.K., Mohanakrishnan D., Sahal D. Antiplasmodial activity of botanical extracts against Plasmodium falciparum. Res. 2011;108:1099
65. Jain N.K., Lodhi S., Jain A., Nahata A., Singhai A.K. Effect of Phyllanthus acidus (L.) Skeels fruit on carbon tetrachloride- induced oxidative damage in livers of rats and mic J Chin Integr Med. 2011; 9(1): 49-56
66. JainK., Singhai A.K. Protective effects of Phyllanthus acidus (L.) Skeels leaf extracts on acetaminophen and thioacetamide induced hepatic injuries in Wistar rats. Asian Pacific Journal of Tropical Medicine. 2011;4:470-474
67. LeeY., Peng W.H., Cheng H.Y., Chen F.N., Lai M.T., Chiu T.H. Hepatoprotective effect of Phyllanthus in Taiwan on acute liver damage induced by carbon tetrachloride.  The American Journal of Chinese Medicine. 2006; 34(3):471-482
68. Padmapriya N., Poonguzhali T.V. Antibacterial and antioxidant potential of the acetone extract of the fruit of Phyllanthus acidus Int. J. Curr. Sci. 2015; 17: E64-E72.
69. Nguyen T.T.K., Laosinwattana C., Teerarak M., Pilasombut K. Potential antioxidant and lipid peroxidation inhibition of Phyllanthus acidus leaf extract in minced pork. Asian-Australia. J. Anim. Sci. 2017; 30: 1323-1331.
70. Moniruzzaman M., Asaduzzaman M., Hossain M.S., Sarker J., Rahman S.M., Rashid M., Rahman M.M. In vitro antioxidant and cholinesterase inhibitory activities of methanolic fruit extract of Phyllanthus acidus. BMC Complement. Altern. Med. 2015; 15:403-412.
71. Meléndez PA and Capriles Antibacterial properties of tropical plants from Puerto Rico. Phytomedicine. 2006; 13(4):272-276
72. Jagessar R.C., Mars A., Gomes G. Selective Antimicrobial properties of Phyllanthus acidus leaf extract against Candida albicans, Escherichia coli and Staphylococcus aureus using Stokes Disc diffusion, Well diffusion, Streak plate and a dilution method. Nature and Science. 2008; 6(2):24-38
73. Sowmya C., Lavakumar V., Venkateshan N., Ravichandiran,  Saigopal D.V.R. Exploration of Phyllanthus acidus mediated silver nanoparticles and its activity against infectious bacterial pathogen. Chemistry Central Journal. 2018;12:42
74. Chongsaa W., Jansakul Six week’s oral gavage of Phyllanthus acidusleaf water extract decreased visceral fat, the serum lipid profile and liver lipid accumulation in middle-aged male rats. Journal of Ethnopharmacology. 2014;155(1):396-404
75. Chongsaa W., Jansakul Effects of 6 weeks oral administration of Phyllanthus acidusleaf water extract on the vascular functions of middle-aged male rats. Journal of Ethnopharmacology. 2015;176:79-89
76. Uddin M., Mamun A., Hossain M., Ashaduzzaman M., Noor M., Hossain M., Uddin M., Sarker J., Asaduzzaman M. Neuroprotective effect of Phyllanthus acidus on learning and memory impairment in scopolamine-induced animal model of dementia and oxidative stress: natural wonder for regulating the development and progression of Alzheimer’s disease. Advances in Alzheimer’s disease. 2016;5:53-72
77. Chatatikun M., Yamauchi T., Yamasaki K., Chiabchalard A., Aiba S. Phyllanthus acidus(L.) Skeels and Rhinacanthus nasutus (L.) Kurz leaf extracts suppress melanogenesis in normal human epidermal melanocytes and reconstitutive skin culture. Asian Pac J Trop Med. 2019;12:98-105
78. Sousa M., Ousingsawat J., Seitz R., Puntheeranurak S., Regalado A., Schmidt A., Grego T., Jansakul C., Amaral M.D., Schreiber R., Karl K.K. An Extract from the Medicinal Plant Phyllanthus acidus and Its Isolated Compounds Induce Airway Chloride Secretion: A Potential Treatment for Cystic Fibrosis. Molecular Pharmacology. 2007; 71(1):366-376