International Journal of Pharmacology and Pharmaceutical Sciences 2014; Vol: 2, Issue: 2, 20-25 Home Page: http://ijppsjournal.org International Journal of Pharmacology and Pharmaceutical Sciences Review Article REVIEW ARTICLE ISSN: 2394-613X KIGELIA AFRICANA: AN EPHEMERAL GLANCE Gamal Osman Elhasan1,2 Safaa Mohammed omer2, M. U. Khan1, Abdul kareem Mohammed Abdulkareem 2, Habibullah Khalilullah1, 1. Department of pharmaceutics, Unaizah College of Pharmacy, Qassim University, Kingdom of Saudi Arabia 2. Faculty of pharmacy, Omdurman Islamic University, Khartoum- Sudan Corresponding author Abstract Our world harbors a rich source of medicinal plants which are used in the treatment of a wide range of diseases. Kigelia africana popularly known as the Sausage tree, cucumber plant, Kigelia pinnata, is a multipurpose medicinal plant with many attributes and considerable potentials. Some of these include its use for treatment of gynecological disorders, renal ailments, skin complaint, tumors and reproductive disorders in developing countries where western orthodox medicine are expensive and are inaccessible, and there is high poverty rate. Key words: Kigelia Africana, Chemical constituents, Pharmacological Properties. Introduction Nature has been a source of medicinal agents for thousands of years and an impressive number of modern drugs have been isolated from natural sources, many of these isolations were based on the uses of the agents in traditional medicines [1]. This plant-based traditional medicine system continues to play an essential role in health care with about 80% of the world’s inhabitants relying mainly on traditional medicines for their primary health care [2]. Kigelia Africana (Lam.) Benth. syn. K. pinnata (Jacq.) DC. of Bignoniaceae family is widely distributed in the South, Central and West Africa. It is known as the cucumber or sausage tree because of the huge fruits (average 0.6 m in length and 4 kg in weight), which hangs from long fibrous stalks. It is also known as Balmkheera in Hindi and distributed all over India but found abundantly in West Bengal. It is found mostly in wetter areas and spread abundantly across wet Savannah and riverine area [3-6]. Human use of plants as medicine agent pre-dates recorded history. Ethno-medicinal plant-use data in many forms has been heavily utilized in the development of formularies and pharmacopoeias, providing a major focus in global healthcare, as well as contributing substantially to the drug development process [7]. Generally, natural drug substances often form vital and appreciable roles in the modern system of medicine thereby justifying their presence in the prevailing therapeutic arsenal, namely- serve as extremely useful natural drugs, provide basic compounds affording less toxic and more effective drug molecule, modification of inactive natural products by suitable biological and chemical means into potent drugs [8]. Infectious diseases are important in public health for communities in Africa and the developing world [9]. These diseases and subsequent deaths have devastating consequences for developing economies. Herbs have provided us some of the very important lifesaving drugs used in the armamentarium of modern medicine. Among the estimated 400,000 plant species, only 6% have been studied for biological activity and about 15% have been investigated phytochemically [10] . This inadvertently shows a dare need Elhasan GO.,Int. J. Pharmacol. Pharm. Sci. (2015) 2:2; 20-25. 20 for the in-depth dissertation of various chemical constituents, medicinal viability, pharmacological evaluation and biological activities of herbal medicine such as the K. Africana (Lam) Benth (or K. pinnata) of the family Bignoniaceae an exceptional indigenous medicinal plant in Africa. Description of K. Africana tree, fruit, and seed: The tree is widely grown as an ornamental plant in the tropical regions for its decorative flowers and unusual fruit. It can grow to more than 20 m tall. The bark is grey and at first smooth but peels on older trees. The bark can be as thick as 5 mm. The wood is pale brown or yellowish in color, and not prone to cracking [11]. The leaves are opposite or in whorls of 30 to 50 cm in length, pinnate, with six to ten oval leaflets each up to 20 cm in length and 6 cm wide. Some birds/insects are attracted to the flowers where they use the strong stems as footholds. Their scent is most notable at night, indicating their reliance on pollination by bats which visit them for pollen and nectar. It flowers between the months of August and November [12]. Flowers are bisexual, very large; pedicel up to 11 cm long up curved at tip; calyx shortly tubular to campanulate 2 to 4.5 cm long, suddenly widening and incurving upwards, limp 2-lipped, with the super or lip 2-lobed, the lower one 3-lobed and recurved [13]. The huge, grey-brown fruit is a woody berry 30 to 100 cm long and up to 18 cm wide. It weighs between 4 to 10 kg and hangs from a long and fibrous stalk [14]. The fruit is fibrous and pulpy, containing numerous hard seeds which are inedible to humans. However, several species of mammals eat the fruits/seeds, for example baboons, bush pigs, monkeys, porcupines, savannah elephants, giraffes and hippopotami. The seeds are dispersed via their dung. In Malawi, during famine the seeds are roasted and eaten by humans. Brown parrots and brown-headed parrots also eat the seeds [15, 17]. Constituents of K. Africana The understanding of the phytochemical constituents of medicinal plants like K. Africana is imperative not only because of the understanding of the scientific rationale for its usage but also for the discovery of novel compounds of pharmaceutical value [18]. Several phytochemical studies revealed that the extracts from many species of Bignoniaceae contained secondary metabolites such as saponins, tannins, flavonoids, quinones, alkaloids, anthralene derivatives, reducing sugars, glycosides, carbohydrates, querletin, kaempferol, α-sitosterol, terpenes, steroids, coumarins secondary metabolites and their derivatives [19, 20]. These bioactive constituents are reported to be present in the fruits, stem bark, root bark and leaves of K.africanaa and iridoid, verminoside and polyphenols like verbascoside [21- 25]. A notable number of bioactive compounds have been recorded from the Bignoniaceae family of plants that reportedly demonstrates a number of important activities which are beneficial to human beings. The various activities included mosquito larvicidal [26], anti-oxidant [27-30], anti-plasmodial [31], antiprotozoal [32, 33], anti-amoebic [34], antidiarrheal [35-37], anti-inflammatory [3840], anti-microbial [41], antibacterial [42- 46], anti-depressant/central nervous system (CNS) stimulant effects [47], anti-cancer [4852], anti-diabetic, anti-nociceptive, anti-snake venom and neurotrophic [53] activities. However, efforts at the further elucidation of how these activities are executed in vivo or in vitro remains to be established by researchers. Table: 1 Pharmacological activities of different phytoconstituents of KigeliaAfricana Activity Irridoids Naphthoquinone Elhasan GO.,Int. J. Pharmacol. Pharm. Sci. (2015) 2:2; 20-25. Meroterpenoid Coumarin Lignans Sterols Flavonoids 21 Anticancer Mollusicidal Syphilis and Gonorrhea Antidiarrhoeal Antiulcer Antifungal Antimalarial Antiinflammatory /analgesic Antibacterial Postpartum Haemorrhage Pneumonia Conclusion + + + + + naphthoquinones + - derivatives + - + - + + + + + + + + + + + + - + + - + + + + + + + + + - + - + + - + + - + - - - - + + K. Africana is an interesting example of a plant, used in traditional medicine for many years which is now attracting interest and use far beyond its original geographical range. Experiments into the effect of Kigelia extracts and some of the pure compounds contained therein, on microorganisms and cancer cells have shown that the traditional use of this plant is given considerable justification. The chemical constituents of the plant provide molecules, which could be of immense medicinal applications. Considering the many medicinal purposes for which it is used, there is enormous scope for future research on K. africana, and further pharmacological investigation is warranted. Conflict of interest: There is no conflict of interest References: 1. Cordell GA, Biodiversity and drug discovery: asymbiotic relationship, Phytochem 2000; 56: 463-480. 2. Farnsworth NR, Akerele O and Bingel AS. Medicinal plants in therapy, Bull WHO 1985; 63: 965-981 3. Cragg GM and Newman DJ, Medicinals for the millennia, Ann. NY Acad. Sci, 2001;953: 3-25. 4. Heine H, In: Flora of Tropical West Africa, byJ Hutchinson and JM Dalziel (Eds), 2nd Edn,revised by FN Hepper 1963; 2: 385. 5. Sofowara A, The present status of knowledgeof the plants used in traditional medicine inWestern Africa: a medical approach and chemical evaluation, J Ethnopharmacol 1980; 2: 109-118. 6. Sofowora A, Medicinal Plants and Traditionalmedicine in Africa, Published by John Wileyand Sons Ltd, IstEdn 1982; 131: 168 -171. 7. Graham JG, Quinn ML, Fabricant DS, Farnsworth NR. Plants used against cancer – an extension of the work of Jonathan Hartwell. J. Ethnopharmacol 2000; 73: 347-377. 8. Kan A. Pharmacognasy and pharmaBiotecnology. New Age International Ltd., New Delhi 2006; 5-11. 9. Sparg SG, Van SJ, Jager AK. Efficiency of traditionally used South African Plants against Schistosomiasis. J. Ethnopharmacol 2000; 73: 209-214. Elhasan GO.,Int. J. Pharmacol. Pharm. Sci. (2015) 2:2; 20-25. 22 10. Cragg GM, Newman DJ, Sander KM. Natural Products in Drug Discovery and Development. J. Nat. Prod 1997; 60: 5260. 11. Roodot V. Kigelia africanain: The Shell Field Guide to the Common Trees of the Okavango Delta and Moremi Game Reserve. Gaborone, Botswana: Shell Oil Botswana 1992; 43. 12. Joffe P. Kigelia Africana (Lam) Benth. Pretoria National Botanical Garden 2003. (www.plantzafrica.com). 13. Grace OM, Light ME, Lindsey KL, Moholland DA, Staden JV, Jager AK. Antibacterial activity and isolation of antibacterial compoundsfrom fruit of the traditional African Medicinal plant, Kigelia africana. S.Afr. J. Bot 2002; 68:220222. 14. Azu OO. The role of Kigelia Africana fruit extract against cisplatin-induced testicular damage in Sprague-Dawley rats. PhDThesis, University of Lagos, Nigeria p 2010; 163. 15. delHoyo J, Elliot A and Sargatal J eds. Handbook of the birds of the world Lynx Editions 1997; 4: 415. 16. Mukherjee P. Quality Control of Herbal Drugs.Eastern Publishers (Business Horizons Ltd.) New Delhi, ISBN 819007884-4. 2002; 16. 17. Owolabi OJ, Omogbai EKI, Obasuyi O. Antifungal and antibacterial activities of ethanolic and aqueous extract of Kigelia africana (Bignoniaceae) stem bark. Afr. J. Biotechnol 2007; 6:1677-1680. 18. Fennell CW, Lindsey KL, McGaw LJ, Sparg SG, Stafford GI, ElgorashiEE, Grace OM, van Staden J. Assessing African medicinalplants for efficacy and safety: pharmacological screening andtoxicology. J. Ethnopharmacol 2004; 94:205-217. 19. Gouda YG, Abdel-Baky AM, Darwish FM, Mohamed KM, Kasai R, Yamasaky K. Phenylpropanoid and phenylethanoid derivatives From Kigelia pinnata D.C. Fruits. Nat. Prod. Res 2006; 10: 935-939. 20. Choudhury S, Datta S, Talukdar AD, Choudhury MD. Phytochemistry of the Bignoniaceae-A review. Biol. Environ. Sci 2011; 1: 145-150. 21. Picerno P, Autore G, Marzocco S, Meloni M, Sanogo R, Aquino RP. Anti-inflammatory activity of verminoside from Kigelia Africana and evaluation of cutaneous irritation in cell cultures and reconstituted human epidermis. J. Nat. Prod 2005; 68: 1610-4. 22. Gouda YG, Abdel-Baky AM, Darwish FM, Mohamed KM, Kasai R, Yamasaky K. Phenylpropanoid and phenylethanoid derivatives From Kigelia pinnata D.C. Fruits. Nat. Prod. Res 2006; 10: 935-939. 23. Sofowara A. Medicinal plants and traditional medicine in Africa. John Wiley, Chichester 1984; 142-145. 24. Binutu OA, Adesogan K, Okogun JI. Constituents of Kigelia pinnata. Nig. J. Nat. Prod. Med. Pp 1997; 1-68. 25. Weiss CR, Moideen SV, Houghton PJ. Activity of extacts and isolated naphthoquinones from Kigeliapinnata against plasmodium falciparum. J. Nat. Prod 2000; 9: 1306-9. 26. Taura DW, Mukhtar MD, Adoum OA. Lethality of the aqueous extracts of Acacia nilotica, Guierasenegalensis, Kigelia Africana and Securidacalongepedunculata on culex mosquito larva. Ife J. Sci 2004; 6: 115-118. 27. Oltof MR, Hollman PCH, Katan MB. Chlorogenic acid, caffeic acids are absorbed in humans. J. Nutr 2001; 131: 66-71. Elhasan GO.,Int. J. Pharmacol. Pharm. Sci. (2015) 2:2; 20-25. 23 28. Jung UJ, Lee MK, Park YB, Jeon SM, Choi MS.Antihyperglycemic and Antioxidant Properties of Caffeic Acid in db/dbMice.Journal of Pharmacology and Experimental Therapeutics Fast Forward. J. Pharmacol. Exp. Ther 2006; 318: 476-483. 29. Olaleye MT, Rocha JB. Commonly used tropical medicinal plants exhibit distinct in vitro antioxidant activities against hepatotoxins in rat liver. Exp. Toxicol. Pathol 2007;58:433-438. 30. Olaleye MT, Rocha BT. Acetaminophen-induced liver damage in mice: Effects of some medicinal plants on the oxidative defence system. Exp. Toxicol. Pathol 2008; 59:319-327. 31. Zofou D, Kengne ABO, Tene M, Ngemenya MN, Tane P, Titanji VPK. In vitro antiplasmodial activity and cytotoxicity of crudeextracts and compounds from the stem bark of Kigelia Africana (Lam Benth (Bignoniaceae). Parasitol. Res 2011; 108:1383-1390. 32. Moiden SV, Houghton PJ, Rock P, Croft SL, Aboagye-Nyame F. Activity of extracts and naphthoquinones from Kigelia pinnata against Trypanosomabruceibrucei and Trypanosomabruceirhodesiense.Planta Med 1999; 65: 536-540. 33. Weiss CR, Moideen SV, Houghton PJ. Activity of extacts and isolated naphthoquinones from Kigeliapinnata against plasmodium falciparum. J. Nat. Prod 2000; 9: 1306-9. 34. Bharti N, Singh S, Naqvi F, Azam A. Isolation and in vitro antiamoeboic activity of iridoids isolated from Kigeliapinnata. General Papers ARKIVOC x 2006;69-76. 35. Galvez J, Zarzuelo A, Crespo ME, Lorente MD, Ocets MA, Jimenez J. Anti-diarrheal activity of Euphorbia hirta extract and isolation of an active flavonoid constituent.PlantaMedica 1993; 59: 333 – 336. 36. Akah PA. Antidiarrheal activity of Kigelia africanain experimental animals. J. Herbs Spices Med. Plants 1998; 4: 31-38. 37. Owolabi OJ, Omogbai EKI. Studies on the antidiarrhoeal properties of the ethanolic extract of Kigelia Africana (Bignoniaceae).Pharmacologyonline 2009; 1: 243-251. 38. Picerno P, Autore G, Marzocco S, Meloni M, Sanogo R, Aquino RP. Anti-inflammatory activity of verminoside from Kigelia Africana and evaluation of cutaneous irritation in cell cultures and reconstituted human epidermis. J. Nat. Prod 2005; 68: 1610-4. 39. Hussain H, Krohn K, Ahmad VU, Miana GA, Green IR. Lapachol: an overview. Reviews and Accounts ARKIVOC ii: 2007; 145-171. 40. Akunyili DN, Houghton PJ, Raman A. Antimicrobial activities of the stem bark of Kigeliapinnata. J. Ethnopharmacol 1991; 35:173-177. 41. Binutu OA, Adesogan K, Okogun JI. Constituents of Kigelia pinnata. Nig. J. Nat. Prod. Med. Pp 1997; 1-68. 42. Binutu OA, Adesogan K, Okogun JI. Constituents of Kigelia pinnata. Nig. J. Nat. Prod. Med. Pp 1997;1-68. 43. Grace OM, Light ME, Lindsey KL, Moholland DA, Staden JV, Jager AK. Antibacterial activity and isolation of antibacterial compoundsfrom fruit of the traditional African Medicinal plant, Kigelia africana. S.Afr. J. Bot 2002; 68: 220222. Elhasan GO.,Int. J. Pharmacol. Pharm. Sci. (2015) 2:2; 20-25. 24 44. Ogbeche KA, Ogunbiyi YO, Duru FIO. Effect of Methanol extract of Kigelia Africana on sperm motility and fertility in Rats. Nig. J.Health Biomed. Sci 2002; 2: 113-116. 45. Hussain H, Krohn K, Ahmad VU, Miana GA, Green IR. Lapachol: an overview. Reviews and Accounts ARKIVOC ii: 2007; 145-171. 46. Owolabi OJ, Omogbai EKI, Obasuyi O. Antifungal and antibacterial activities of ethanolic and aqueous extract of Kigelia africana (Bignoniaceae) stem bark. Afr. J. Biotechnol 2007; 6: 1677-1680. 47. Owolabi OJ, Amaechina FC, Eledan AB.Central nervous systemstimulant effect of the ethanolic extract of Kigelia Africana. J. Med.Plants Res 2008; 2: 20-23. 48. Houghton PJ, Photiou A, Uddin S, Shah P, Browning M, Jackson SJ,Retsas S. Activity of Kigelia pinnata against melanoma and renal carcinoma cell lines. Planta Med 1994; 60:430-433. 49. Jackson SJ, Houghton PJ, Restsas S, Photiou A. In vitro cytotoxicity of norvibutinal and isopinnatal from Kigeliapinnata against cancer cell lines. Planta Med 2000; 66: 758-61. 50. Picerno P, Autore G, Marzocco S, Meloni M, Sanogo R, Aquino RP. Anti-inflammatory activity of verminoside from Kigelia Africana and evaluation of cutaneous irritation in cell cultures and reconstituted human epidermis. J. Nat. Prod 2005; 68: 1610-4. 51. Bharti N, Singh S, Naqvi F, Azam A. Isolation and in vitro antiamoeboic activity of iridoids isolated from Kigeliapinnata. General Papers ARKIVOC x: 2006; 69-76. 52. Hussain H, Krohn K, Ahmad VU, Miana GA, Green IR. Lapachol: an overview. Reviews and Accounts ARKIVOC ii: 2007; 145-171. 53. Rahmatullah M, Samarrai W, Jahan R, Rahman S, Sharmin N, EmdadUllahMiajee ZUM, Chowdhury MH, Bari S, Jamal F, Anwarul Bashar ABM, Azad AK, Ahsan S. An Ethno-medicinal, pharmacological and phytochemical review of some Bignoniaceaefamily plants and a description of Bignoniaceae plants in folk medicinal uses in Bangladesh. Adv. Nat. Appl. Sci 2010; 3: 236-253. Elhasan GO.,Int. J. Pharmacol. Pharm. Sci. (2015) 2:2; 20-25. 25
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