Gopinath G, Thirumal M*, P. R. Kumar
Department of Pharmacognosy, SRM College of Pharmacy, Kattankulathur - 603203
Holarrhena antidysenterica belongs to the family Apocynaceae is commonly known as kurchi in Hindi, Tellicherry bark in English is a small deciduous tree which is distributed throughout the world and in India, it is found in dry forests. In Indian traditional medicine, H. antidysenterica is popularly used as a medication for dysentery, diarrhoea and intestinal worms. Plant parts such as bark are used to treat anti-microbial, anti-inflammatory, analgesics, amoebiasis, chronic bronchitis, locally for boils, ulcers; a decoction of the bark is used in bleeding and piles. The phytochemicals present in the plant include coumarins, ergosterol, flavonoids, phenolic acids, resins, saponins, steroidal alkaloids, tannins, triterpenoids. Pharmacological studies include anti-amnesic, neuroprotective, acetylcholinesterase inhibitory, anti-diabetic, anti-urolithic, antibacterial activity, anti-haemorrhoidal, analgesic activity, anti-inflammatory, anti-malarial, anti-diarrhoeal, anti-mutagenic, antihypertensive activity, antioxidant/free radical scavenging property, diuretic activity, anti-amoebic, anthelminthic, anti-microbial and anti-MRSA properties of Holarrhena antidysenterica. This review article explored the detailed investigation of the botanical description, phytochemistry and pharmacological actions of Holarrhena antidysenterica to afford an objective for further research.
Holarrhena antidysenterica belongs to the family Apocynaceae is commonly known as Kurchi in Hindi, Tellicherry bark in English is a small deciduous tree with white flowers. The plant is distributed throughout the tropical and subtropical regions of the world and in India, it is distributed over the altitudes of up to 4000ft and also found in the dry forest.1-3 In Indian traditional medicine, H. antidysentrica is popularly used as a medication for dysentery, diarrhoea and intestinal worms.1 Plant parts such as bark are used to treat anti-microbial, anti-inflammatory, analgesics,4,5 amoebiasis, chronic bronchitis, locally for boils, ulcers,6 a decoction of the bark is used in bleeding and piles.7 Root and bark were found to be an excellent remedy for acute and chronic dysentery in case of excessive blood with mucous and colic pain with stools.8
Seeds play a major role in Ayurveda for the treatment of flatulence, jaundice, piles, and worms.6 Hydro-alcoholic extracts of seeds were reported to have anti-urolithic activity in both in-vitro and in-vivo methods and it prevents the calcium oxalate crystals aggregation.9 Stem bark was used for skin disease by the tribes of Andhra Pradesh.10 Methanolic extract of stem bark was found to be effective in inflammatory bowel disease.7 Leaves of the plant were claimed to cure scabies.11 The plant is also reported to have anti-diarrhoeal, anti-helminthic, appetizing, asthma, astringent, bronchitis, bronchopneumonia, eczema, epilepsy, fever, jaundice, leprosy, piles and spermatorrhea.12,13 It also possesses immune-modulating agent, larval growth inhibitor property and acts against malaria and vaginitis.8 It contains gut stimulating and inhibitory constituents which mediates its effects through histaminergic and calcium antagonist pathways respectively.10
Holarrhena antidysenterica is a short term tree with a small to a huge height up to 30 to 40 feet producing milky white, thick and less profuse latex. Its leaves are ovate, simple, large, smooth or hairy and opposite to each other. Leaves are 15–30 cm × 4–12cm in size. Its base is obtuse, generally rounded or acute. Leaves nerves are 10 to 14 pairs, opposite and sessile. Its petioles are 1.5cm in length and cymes are 3 to 6cm in diameter. Seeds are 1-2cm long, linear or oblong with long coma shaped or boat-shaped which is light brown to brownish in color and shows epigeal germination. Hairs are present at the apex of the seeds and short-lived. The stem bark of the plant is smooth or rough, pale brown to greyish brown in color which peels off in irregular patches with bitter in taste. The root bark is reddish-brown in color. Plant flowers in the month of April to July which is white, small and arranged in a cluster and glimpse like a flattened top. Petals are disc-shaped and overlay at the right side and corolla 3-4 times longer than calyx; anthers are present inside the corolla tube. It fruits from August to October. The fruits have small, long follicles having white spots on the surface. Dried fruits when busted it releases numerous flat seeds with brown hairs.14-19
Kingdom : Plantae
Subkingdom : Tracheobionta
Super division : Spermatophyta
Division : Magnoliophyta
Class : Magnoliopsida
Subclass : Asteridae
Order : Gentianales
Family : Apocynaceae
Genus : Holarrhena
Species : antidysenterica
Bengal : Kurchi, Kureya
Bombay : Pandhra, Kura
English : Kurchi, Conessi Or Tellicherry Bark
French : Ecoore-De Codagapala
Gujarat : Indrajavanu
Hindi : Karchi, Kura
Punjab : Kewar, Kura
Sanskrit: : Kutaja, Kalinga, Vatsika, Girimallika
Tamil : Kashappu, Vetpalarishi, Veppalai
Telugu : Kaka, Kodise
Chemical constituent’s present in Holarrhena antidysenterica was found mostly in the stem, leaves, bark, and seeds. The primary phytoconstituents are coumarins, ergosterol, flavonoids, phenolic acids, resins, saponins, steroidal alkaloids, tannins, triterpenoids.21-23 The alkaloids discovered from different parts of plants are indexed below.
From stem bark and seeds:
20-Aminoconanines, 3-Aminoconanines, 3,20-Diaminopregnanes, 3-Aminopregnans, Conanines, Conarrhimine [C21H34N2], Conessimine/Isoconessimine [C23H38N2], Conessine [C24H40N2], Isoconessine [C24H40N2] and their derivatives. A new steroidal alkaloid was also extracted, characterized and named as holadysenterine corresponded to the molecular formula [C23H38N2O3].24,25
From stem bark:
(20)-N-Methylholarrhimine [C22H38N2O], (3)-N-Methylholarrhimine[C22H38N2O], 3a-Aminoconan-5-ene [C22H36N2], 7α-Hydroxyconessine [C24H40N2O], Conamine [C22H36N2], Conessidine [C21H32N2], Conkurchine [C20H32N2], Conkurchinine [C25H36N2], Di-hydro-isoconessimine [C23H40N2], Holacetine [C21H32N2O3], Holacine [C26H44N2O2], Holadiene [C22H31NO], Holadysenterine [C23H38N2O3], Holadysone [C21H28O4], Holafrine [C29H46N2O2], Holarrhenine [C24H40N2O], Holarrhessimine [C22H36N2O], Holarrhidine [C21H36N2O], Holarrhimine/Kurchicine [C21H36N2O], Holarrhine [C20H38N2O3], Holarrifine [C24H38N2O2], Holonamine, Kurchamide, Kurchamine [C22H36N2], Kurchenine [C21H32N2O2], Kurchessine [C25H44N2], Kurchilidine [C22H31NO], Kurchimine [C22H36N2], Kurchinidine [C21H29NO2], Kurchinine [C19H24O3], Kurcholessine, Lettocine [C17H25NO2], Neoconessine (isomer of conessine) [C24H40N2], NNN’N’-Tetramethylholarrhimine [C25H44N2O], Norholadiene [C21H29NO], Pubadysone [C21H26O3], Pubamide [C21H27NO3], Pubescimine [C24H40N2O], Pubescine [C22H26N2O4], Puboestrene [C20H24O3], Regholarrhenine A [C22H31NO2], Regholarrhenine B [C21H29NO2], Regholarrhenine C [C22H34N2], Regholarrhenine D [C23H38N2O], Regholarrhenine E [C25H44N2O2], Regholarrhenine F [C25H44N2O], Trimethylconkurchine [C24H38N2].5,22-24,26-30
Following compounds were isolated and reported from the leaves namely Holarosine A [C30H47NO6], Holarosine B [C30H47NO6], Holarricine [C21H32N2O3], Holantosine-A [C28H47NO6], Holantosine-B [C28H45NO5], Holantosine-C [C28H47NO6], Holantosine-D [C28H45NO5], Holantosine-E [C28H47NO6], Holantosine-F [C28H45NO5],21 Kurchiphyllamine, Kurchaline,31 Kurchiphylline [C23H47NO2].27
Antidysentericine [C23H36N2O],24,32 Conimine [C22H36N2]33 were isolated and reported.
Ethanolic extract of seeds administered for 28 days to the independent groups of STZ moderately diminished the level of AChE when compared to the diseased group, blocked the elevation in MDA levels and GSH reduction in a dose-dependent manner. Cholinergic dysfunction was resolved by acetyl cholinesterase activity. Decreased level of AChE, prevented levels of MDA and Glutathione exhibited the anti-amnesic property of Holarrhena antidysenterica.34
Treatment with Methanolic Extract of Holarrhena antidysenterica (MEHA) moderately prevented in bodyweight reduction when compared to the diabetic control group, rise in blood glucose and moderate depletion in plasma cholesterol. HbA1C level was studied as a key indicator of AGEs and in the present study treatment with MEHA inhibited this raised level of HbA1c. MEHA treated rats demonstrated development in locomotion when compared to their non-treated group indicate the avoidance of diabetic neuropathy.35
The alkaloidal extract of seed was found to have 91% inhibition of acetylcholine esterase.36,37 The entire alkaloid extract from seeds actively inhibits the acetyl cholinesterase with an inhibitory concentration of 6.1 μg/mL, except huperzine A which shows inhibition at an inhibitory concentration of 0.015μg/mL.25
Plant Extracts contains a potential anti-diabetic effect.38,39 Ethanolic extract of plant moderately decreased plasma glucose levels 30mins after administration to rats which has normal glucose level. The total cholesterol, triglyceride, AST, ALT, urea and serum creatinine and blood glucose level was decreased by both ethanolic and methanolic extract of the plant.5,40 These parameters indicate that plant possess better metabolic control and potent anti-diabetic effect.
Hepatic glucose-6-phosphatase is an essential enzyme in glucose homeostasis which is regulated by insulin in a negative way.41,42 Due to inulin recovery, the significant recovery of these biosensors was observed post administration of aqueous extract of the plant.43 Phenolic compounds and flavonoids present in the plant extracts are responsible for the resistance of α-glucosidase activity and subsequently suppress glucose absorption in regarding the control of postprandial hyperglycemia.44,45
Hydro-methanolic extracts of seed moderately reduce the intensity of calcium oxalate crystals and convert them into calcium oxalate dehydrate from calcium oxalate monohydrates (COM) in vitro and thereby conceal COM induced cell toxicity and lactate dehydrogenase production. After administration of extract in male Wistar rats, there is a considerable reduction in polyuria, water consumption, calcium ions excretion and crystal formation.8
Anti-bacterial activity and anti-haemorrhoidal action:
Bark, seeds, callus extracts of the plant possess promising antibacterial activity over Staphylococcus, Salmonella and E. coli.7 The plant also inhibited adhesion of enteropathogenic E.coli on host epithelial cells.46,47
“Kutaja tvak churna” an ayurvedic preparation of stem bark extract exhibited healing property in bleeding piles.48
Analgesic Activity and Anti-inflammatory:
Carrageenan induced rat paw edema was inhibited by the methanolic leaf extract of the plant. Furthermore, it also suppressed the writhing response in a dose-dependent manner induced by acetic acid and demonstrated the analgesic efficacy by improving tail-flick latency.15,49 Ethanolic plant extract showed an analgesic effect by suppressing writhing response in albino mice.50,51 H. antidysenterica treatment also prevented rupture of goblet cells, inflammatory cellular infiltration and inflammation in mucosal layer.6
Conessine extracted from the stem bark of the plant exhibited the effective anti-plasmodial property, with the reproducible inhibitory concentration of 1.3μg/ml in-vitro experiments and in-vivo experiment 88.95% suppression of parasitemia when administered at 10 mg/kg. Bark extract exhibited significant results in-vitro study and exhibited anti-malarial property resistance to Plasmodium falciparum and Plasmodium berghei affected albino mice in-vivo.33 Due to malarial infection, increased level of alkaline phosphatase (ALP) and bilirubin were observed which indicates the hepatocytic damage.52,53
Castor oil and E.coli induced diarrhoea in rats when treated with ethanolic extract of seed exhibited an increase in density of their dry feces and suppression in defecation drops.15 Aqueous extract and alcoholic extracts of bark were well-known to resist entero invasive E. coli (EIEC), Salmonella enteritidis, Shigella boydii, and Shigella flexneri.54 In rats diarrhoea were induced by castor oil, a marketed preparation of H. antidysenterica, kutaja parpati vati revealed significant reduction in watery diarrhoea and motility of small intestine content. Moreover, it showed significant 67.55% protection against castor oil-induced enter polling.55
Anti-mutagenic and Anti-hypertensive Activity:
Methanolic extract of plant bark was found to exhibit anti-mutagenic efficiency in mutagenicity induced Salmonella typhimurium strains.56 Inhibition of adequate 24% angiotensin-converting enzyme (ACE), after administration of ethanolic extracts of plant seed, was revealed.57 For antihypertensive activity, Endophytes were obtained from the fungal extract of H. antidysenterica and dissolved in 20% methanol, which exhibited 60% angiotensin-converting enzyme (ACE) inhibition.58
Antioxidant/free radical scavenging property:
Oxidative damage of the tissues was healed and protected by free radical scavenging compounds. In a recent study methanolic leaf extracts of plant exhibits the anti-oxidant property that scavenges superoxide ions and OH- ions with less ability to convert ferric ion to ferrous ion. Further, these effects were observed to be equivalent to the concentration of the extract.14 Aqueous methanolic extract of seed was observed to inhibit deoxyribose degradation by OH- ions, deterioration of H2O2, nitrite formation by facing O2and lipid peroxidation, all the above from the fraction extracted from ethyl acetate.59
Excess of urine output was recognized in Wistar rats after application of aqueous seed extracts of the plant at dose varied from 30 to100mg/kg. A considerable rise in the volume of sodium and potassium ions released through urine was observed.60,61
Routine consumption of the bark powder for two weeks entirely retained patients with amoebiasis. “Amoebian cap”, a medication for amoebiasis contains one of the constituents from plant H. antidysenterica was studied for its therapeutic effect against amoebiasis.62,63
Anthelminthic and anti-microbial activity:
Aqueous extract and ethanolic extracts of plant bark on earthworm exhibited considerable outcome in-vitro activity. Ethanolic extracts of seed exhibited resistance to EPEC bacteria depending on the concentration of extract. Since EPEC exhibited resistance to numerous antibiotics, the ethanolic extract is investigated as a potent antibacterial agent.48,64 In a later study, pet.ether bark extract was found to inhibit E. coli at a minimum inhibitory concentration (MIC) of 50mg/ml simultaneously methanol and chloroform extracts inhibit at higher concentrations. Yet Holarrhena antidysenterica exhibited significant activity when compared to other plants.65
Plant bark extract was found to possess Anti-methicillin resistant Staphylococcus aureus (Anti-MRSA) property at inhibition zone size varied from 11- 44mm and minimum inhibitory concentration ranged from 0.32-3.25mg/mL.66
Hepatoprotective effect and Anti-convulsant activity:
A study revealed that treatment of plant likely to reduce the severity of liver damage, the formation of fibrous septa and also restricts liver weight loss induced by PCM. Therefore, the plant is considered as prevailing hepatoprotective agent.67 Ethanolic extract of the plant exhibited the anticonvulsant activity in mice and hence possesses promising anticonvulsant activity against MES and PTZ induced seizures.68
Ailments have been related to people since their existence. There are enormous measures of natural medications that are stay covered up for the decades. Holarrhena antidysenterica is a promising medicinal plant with a wide scope of pharmacological activities which could be used in a few therapeutic applications due to its efficacy and safety. H.antidysenterica has been generally used to treat ailments like looseness of the bowels, diarrhoea, inflammation, anti-oxidant and against the malarial activity. This plant contains unidentified chemical constituents that are valuable for pharmacists to synthesize and formulate novel medications for different infections.
The authors are grateful to the Dean and faculties of SRM College of Pharmacy SRMIST, Kattankulathur for the facilities.
CONFLICT OF INTEREST:
The authors declare no conflict of interest.
1. Kavitha D, Shilpa P N, Niranjali Devaraj S. Antibacterial and antidiarrhoeal effects of alkaloids of Holarrhena antidysenterica WALL. Indian Journal of Experimental Biology. 2004 Jun; 42: 589-594
2. Gopal, Chauhen MG, Holarrena antidysenterica-A review Suppl to cultivation and utilisation of medicinal plants, Ed Handa SS, Kaul MK, Jammu Tawi, Regional research laboratory; 223-41, (1996).
3. Mrinal, Navjeet Singh. A Review on Pharmacological Aspects of Holarrhena antidysenterica. Scholars Academic Journal of Pharmacy. 2018 Dec; 7(12): 488-492
4. Warrier PK, Nambiar VP, Ramankutty C. Indian medicinal plant: A compendium of 500 species, Orient Longman, Delhi, 1994, 191-194.
5. Sharma PC, Pyelne MB, Dennis TJ. Database on medicinal plants used in ayurveda, Vol 2, Central council for research in ayurveda and siddha, New Delhi, 2004,550.
6. Umashanker KPD, Chandra S, Sharma J. Antidiabetic Efficacy of Ethanolic Extract of Holarrhena antidysenterica Seeds in Streptozotocin – Induced Diabetic Rats and Its influence on certain Biochemical Parameters. Journal of Drug Delivery and Therapeutics. 2012 Jun; 2(4): 159-162.
7. Darji VC, Deshpande S, Bariya AH. Comparison between the effect of aqueous and methanolic extracts of Holarrhena antidysenterica bark against experimentally induced inflammatory bowel disease. International Research Journal of Pharmacy. 2013; 4 (1): 131-134.
8. Mahato S, Mehta A and Roy S. Studies on antibacterial effects of bark, seed and callus extracts of Holarrhena antidysenterica wall. The Bioscan. 2013; 8(2): 717-721.
9. Khan A, Khan S R, Gilani A.H, Studies on the in vitro and in vivo antiurolithic activity of Holarrhena antidysenterica. Urol. Res. 2012 Dec; 40(6): 671-681.
10. Rajalakshmi C. GC-MS analysis of the bark of Holarrhena antidysenterica. Journal of Pharmacognosy and Phytochemistry. 2018; 7(4): 797-800
11. Prajapati ND, Purohit SS, Sharma AK, et al. A Handbook of Medicinal Plants. Jodhpur, India: Agrobios Publishers; 2004. p 273.
12. Bhattacharjee SK, Handbook of Medicinal Plants Jaipur, India: Pointer Publishers 2000; p 183.
13. Guha Bakshi DN, P Sensarma and DC Pal A, Lexicon of Medicinal Plants in India (2001) (Vol II), Calcutta, India: Naya Prokash Publishers; p 356-358.
14. Jamadagni PS, Pawar SD, Jamadagni SB, Chougule S, Gaidhani SN and Murthy SN. Review of Holarrhena Antidysenterica (L.) Wall. Ex A. DC. Pharmacognostic, Pharmacological, and Toxicological Perspective. Pharmacognosy Review. 2017; 11(22): 141–144.
15. Ganapathy PS, Ramachandra YL, Rai SP. In vitro antioxidant activity of Holarrhena antidysenterica Wall. Methanolic leaf extract. Journal of Basic and Clinical Pharmacy. 2011 Nov; 2(4): 175-178.
16. Sharma DK, Gupta VK, Kumar S, Joshi V, Mandal RSK, Prakash AGB, Singh M. Evaluation of antidiarrhoeal activity of ethanolic extract of Holarrhena antidysenterica seeds in rats. Veterinary World. 2015 Dec; 8(12): 1392-1395.
17. Dictionary of Indian Medicinal Plants, CIMAP, Lucknow (1992).
18. Ali Shah SM, Khan Usmanghani, Naveed Akhtar, Asif HM, Akram M, Khalil Ahmed, Ghazala Shaheen, Tahira shamim, Riazur Rehman, Ashfaq Ahmad, Laila Sumreen. Monograph of Holarrhena antidysenterica (Linn.) Wall. International Journal of Phytomedicine 2 (2010); 345-348
19. Mohammed Rahmatullah, Baharul Islam, Arif Khan Md, Shoma JF, Taufiq Rahman. “Holarrhena antidysenterica (Linn.) Wall. (Apocynaceae) – A Plant for Gastrointestinal Disorders”. EC Gastroenterology and Digestive System 5.6 (2018): 437-443.
20. Nadkarni KM. Indian plants and drugs. New Delhi. Ajay Book Service Publishers. 2010.
21. Dev S. A Selection of Prime Ayurvedic Plant Drugs: Ancient-modern Concordance. New Delhi: Anamaya; 2006.
22. Alauddin M, Martin-Smith M. Biological activity in steroids possessing nitrogen atoms. Journal of Pharmacy and Pharmacology. 1962; 14: 469-495.
23. Daniel M. Medicinal Plants: Chemistry and Properties. Enfield, NH: Science; 2006.
24. Kumar N, Singh B, Bhandari P, Gupta AP, Kaul VK. Steroidal alkaloids from Holarrhena antidysenterica (L.) WALL. Chemical and Pharmaceutical Bulletin. 2007 Jun; 55(6): 912-914.
25. Yang ZD, Duan DZ, Xue WW, Yao XJ, Li S. Steroidal alkaloids from Holarrhena antidysenterica as acetylcholinesterase inhibitors and the investigation for structure–activity relationships. Life Sciences. 2012; 90: 929-933.
26. Stephenson RP. The pharmacological properties of conessine, isoconessine and neoconessine. British Journal Pharmacology. 1948; 3: 237-245.
27. Usmani SB. Studies on the Chemical Constituents of Holarrhena antidysenterica L. and the b-carboline Series of Bases and Their Pharmacological Activity. Thesis. Pakistan: H.E.J. Research Institute of Chemistry, University of Karachi; 1995.
28. Chakraborty A, Brantner AH. Antibacterial steroid alkaloids from the stem bark of Holarrhena pubescens. Journal of Ethanopharmacology. 2000 Jan; 68(1-3): 339-344.
29. Siddiqui BS, Usmani SB, Ali ST, Begum S, Rizwani GH. Further constituents from the bark of Holarrhena pubescens. Phytochemistry. 2001; 58: 1199-1204.
30. Lather A, Gupta V, Bansal P, Singh R, Chaudhary AK. Pharmacological potential of ayurvedic formulation: Kutajghan-Vatie A review. Journal of Advanced Scientific Research. 2010; 1(2): 41-45.
31. Panda SK, Patra N, Sahoo G, Bastia AK, Dutta SK. Antidiarrhoeal activities of medicinal plants of Similipal Biosphere Reserve, Odisha, India. International Journal of Medicinal and Aromatic Plants. 2012; 2(1): 123-134.
32. Kumar A, Ali M. A new steroidal alkaloid from the seeds of Holarrhena antidysenterica. Fitoterapia. 2000; 71: 101-104.
33. Verma G, Dua VK, Agarwal DD, Atul PK. Anti-malarial activity of Holarrhena antidysenterica and Viola canescens, plants traditionally used against malaria in the Garhwal region of north-west Himalaya. Malaria Journal. 2011;10(20): 1-5
34. Mrinal, Navjeet Singh, Nitin Bansal. Anti-amnesic Activity of Holarrhena Antidysenterica Extract in Streptozotocin-Induced Memory Deficient Rats. Scholars Academic Journal Pharmacy. 2016; 5(8): 317-325.
35. Bansal N, Singh N, Mrinal. Holarrhena Antidysenterica Extract Promotes Recovery of Peripheral Neuropathy in Diabetic Rats. American Journal of Pharma Tech Research. 2016; 6(4): 2249-3387.
36. Ellman GL, Courtney KD, Andres V, Featherstone RM. A new and rapid colorimetric determination of acetylcholinesterase activity. Biochemical Pharmacology. 1961; 7(2): 88-95.
37. Orhan I, Sener B, Choudhary MI, Khalid A. Acetylcholinesterase and butyrylcholinesterase inhibitory activity of some Turkish medicinal plants. Journal of Ethnopharmacology. 2004; 91(1): 57-60.
38. Kazi MA, Tushar KB, Suvra M, Bikash RB, Debidas G. Attenuation of diabetic disorders in experimentally induced diabetic rat by methanol extract of seed of Holarrhena antidysenterica. International Journal of Pharma Tech Research. 2010; 1: 1205-1211.
39. Pradeep Sahu, Anindh Sharma, Tanushree Chatterjee. Natural Products with Potent Hypoglycemic Activity. Research J. Pharm. and Tech.3 (3): July-Sept. 2010; Page 650-656
40. Mana S, Singhal S, Sharma NK, Singh D. Hypoglycemic Effect of Holarrhena antidysenterica Seeds on Streptozotocin induced Diabetic Rats. International Journal of Pharma Tech Research. 2010; 2(2): 1325-1329.
41. Berg JM, Tymoczko JL, Stryer L. Glycolysis and gluconeogenesis. In: Biochemistry. Berg JM, Tymoczko JL, Stryer L. (Eds). W.H. Freeman: New York. 2001; 425-464.
42. Das D. 2002. Biochemistry, 11th edition, Kolkata, Academic Publishers, p-448.
43. Ali KM, Chatterjee K, De D, Bera TK, Ghosh D. Efficacy of aqueous extract of seed of Holarrhena antidysenterica for the management of diabetes in experimental model rat: A correlative study with antihyperlipidemic activity. International Journal of Applied Research in Natural Products. 2009; 2(3): 13-21.
44. Ali KM, Chatterjeea K, Dea D, Janaa K, Beraa TK, Ghosha D. Inhibitory effect of hydro-methanolic extract of seed of Holarrhena antidysenterica on alpha-glucosidase activity and postprandial blood glucose level in normoglycemic rats. Journal of Ethnopharmacology. 2011; 135: 194–196.
45. Monago Comfort C., Nwodo O. Fred C. Antidiabetic Effects of Crude Flavanoid and Alkaloid of Abrus precatorius Linn Seed in Alloxan Diabetic Rabbits. Research J. Pharmacognosy and Phytochemistry 2010; 2(4): 331-335.
46. Kavitha D, Niranjali S. Inhibition of enteropathogenic Escherichia coli adhesion on host epithelial cells by Holarrhena antidysenterica (L.) WALL. Phytotherapy Research, 2009; 23: 1229–1236.
47. Premlata Singariya, Krishan Kumar Mourya, Padma Kumar. Estimation of Antibacterial Efficacy in Alkaloids of Anogeissus rotundifolia an Indigenous Medicinal Plant against Some Pathogenic Micro-organisms. Asian J. Research Chem. 2018; 11(2):432-440.
48. Pal A, Sharma PP, Mukherjee PK. A clinical study of Kutaja (Holarrhena antidysenterica Wall) on Shonitarsha. An International Quarterly Journal of Research in Ayurveda. 2009; 30(4): 369-372.
49. Pankaj Rakha, Manju Nagpal, Sunil Sharma, Milind Parle. Anti-Inflammatory Activity of Petroleum Ether Extract of Seeds of Ocimum Basilicum Linn. Research J. Pharm. and Tech.2 (3): July-Sept. 2009,;Page 589-591.
50. Shwetha C, Latha KP, Asha K. Study on analgesic activity of Holarrhena antidysenterica leaves. International Journal of Herbal Medicine. 2014; 2(3): 14-16.
51. Manpreet Kaur, Harinder Kaur. Analgesic Activity of Roots of Aralia racemosa. Research J. Pharm. and Tech. 4(12): Dec. 2011; Page 1896-1897.
52. Dua VK, Verma G, Singh B, Rajan A, Bagai U, Agarwal DD, Gupta NC, Kumar S, Rastogi A. Anti-malarial property of steroidal alkaloid conessine isolated from the bark of Holarrhena antidysenterica. Malaria journal. 2013 Dec; 12(1): 194.
53. Takate S.B, Pokharkar R.D, Chopade V.V. Gite V.N. Hepatoprotective Activity of the Water Extract of Launaeaintybacea (Jacq)Beauv in Paracetamol Induced Hepato-Toxicity in Albino Rats. Research J. Pharm. and Tech.2010; 3(3):p.815-817
54. Dey A, De JN. Ethnobotanical Survey of Purulia district, West Bengal, India for medicinal plants used against gastrointestinal disorders. Journal of Ethnopharmacology. 2012; 143: 68-80.
55. Gupta K, Karale S, Warad V. Anti-diarrhoeal activity of a polyherbal formulation in various animal models of diarrhoea. International Research Journal of Pharmacy. 2012; 3(8): 289-290.
56. Lin J, Opoku AR, Geheeb-Keller M, Hutchings AD, Terblanche SE, Jager AK, Van Staden J. Preliminary screening of some traditional Zulu medicinal plants for anti-inflammatory and antimicrobial activities. Journal of Ethnopharmacology. 1999; 68: 267-274.
57. Somanadhan B, Varughese G, Palpu P, Sreedharan R, Gudiksen L, Smitt UW, Nyman U. An ethnopharmacological survey for potential angiotensin converting enzyme inhibitors from Indian medicinal plants. Journal of ethnopharmacology. 1999 May 1; 65(2):103-112.
58. Aqil F, Zahin M, Ahmad I. Antimutagenic activity of methanolic extracts of four ayurvedic medicinal plants. Indian Journal of Experimental Biology. 2008; 46(9): 668-672.
59. Ali KM, Ghosh A, Chatterjee K, Mandal S, Barik B, Pathak TK, Ghosh D. Free radical scavenging activity of seed of Holarrhena antidysenterica: an in vitro study. Journal of Pharmacy Research. 2011; 4(6): 1631-1632.
60. Khan A, Bashir S, Gilani AH. An in vivo study on the diuretic activity of Holarrhena antidysenterica. African Journal of Pharmacy and Pharmacology. 2012 Feb 22; 6(7): 454-458.
61. N Sirisha, M Sreenivasulu, K Sangeeta, G Swarna Latha, A Lakshmi Devi, C Madhusudhana Chetty. A Review on Herbal Diuretics. Research J. Pharm. and Tech. 4(3): March 2011; Page 335-348.
62. Shahabuddin KU, Sarwar MS, Mohiuddin E. Clinical evaluation of some herbal medicine for amoebiasis. Pakistan Journal of Pharmacology. 2006 Jul; 23(2): 9-12.
63. Sunirmal Bhattacharjee, Nilayan Guha, Gouranga Dutta, Manas Chakraborty, Mayukh Jana, Susanta Paul. Formulation and Evaluation of Sustained Release Matrix Tablet of Anti-Amoebic Drug by Natural Polymers. Research J. Pharm. and Tech. 2017; 10(7): 2041-2046.
64. Patil R, Devkar S, Pawar P, Pattewar A. In-vitro anthelminthic activity of Holarrhena antidysenterica bark. International Journal of Pharmaceutical Research and Development. 2012; 4(3): 147-150.
65. Patel JD, Patel DK, Shrivastava A, Kumar V. Screening of plant extracts used in traditional antidiarrhoeal medicines against pathogenic Escherichia coli. Scientific World journal. 2008; 6(6): 63-67.
66. Farrukh A, Iqbal A, Mohd O. Evaluation of anti-methicillin-resistant Staphylococcus aureus (MRSA) activity and synergy of some bioactive plant extracts. Biotechnology Journal 2006; 1:1093–1102
67. Pritt Verma, Sajal Srivastava, Ch. V. Rao. Hepatoprotective effect of Ethanolic Extract of Holarrhena antidysenterica against Paracetamol Induced Toxicity in Wistar Rats. Research J. Pharm. and Tech 2018; 11(4): 1633-1639
68. Jiban Debnath, Santosh B Dighe, Nachiket S Dighe, Mana Supriya. An Experimental Evaluation of Anticonvulsant Activity of Ethanolic Extract of Seeds of Holarrhena antidysenterica In Mice. Research J. Pharmacology and Pharmacodynamics. 2011; 3(1): 31-33.
Received on 17.08.2019 Modified on 31.10.2019
Accepted on 12.11.2019 © RJPT All right reserved