Antidiarrheal and antinociceptive activities of ethanol extract and its chloroform and pet ether fraction of Phrynium imbricatum (Roxb.) leaves in mice
-
Mohammed Munawar Hossain
, S.M. Zahid Hosen
Abstract
Background:
The objective of the study was to evaluate the antidiarrheal and antinociceptive activities of ethanol extract and its chloroform and pet ether fraction of Phrynium imbricatum (Roxb.) leaves in mice.
Methods:
In the present study, the dried leaves of P. imbricatum were subjected to extraction with ethanol, and then it was fractioned by chloroform and pet ether solvent. Antidiarrheal effects were tested by using castor oil-induced diarrhea, castor oil-induced enteropooling, and gastrointestinal transit test. Antinociceptive activity was evaluated by using the acetic acid-induced writhing test and formalin-induced paw licking test.
Results:
The standard drug loperamide (5 mg/kg) showed significant (p<0.001) inhibitory activity against castor oil-induced diarrhea, in which all the examined treatments decreased the frequency of defecation and were found to possess an anti-castor oil-induced enteropooling effect in mice by reducing both weight and volume of intestinal content significantly, and reducing the propulsive movement in castor oil-induced gastrointestinal transit using charcoal meal in mice. The results showed that the ethanol extract of P. imbricatum leaves has significant dose-dependent antinociceptive activity, and among its two different fractions, the pet ether fraction significantly inhibited the abdominal writhing induced by acetic acid and the licking times in formalin test at both phases.
Conclusions:
These findings suggest that the plant may be a potential source for the development of a new antinociceptive drug and slightly suitable for diarrhea, as it exhibited lower activity. Our observations resemble previously published data on P. imbricatum leaves.
Acknowledgments
The authors are grateful to the authority of the International Islamic University Chittagong, Bangladesh, for providing the facilities to conduct this research work. The authors thank the GUSTO A Research Group for financial support. The authors are also thankful to all members of the GUSTO A Research Group, especially to Mr. Shabbir Ahmed, Department of Pharmacy, IIUC; Mr. Md. Akramul Hoque, Department of Pharmacy, IIUC; and Mr. Nishan Chakrabarty, Department of Pharmacy, IIUC, Bangladesh, for their kind help in the experiments.
Author contributions: MMH and MSHK collected the plant leaves and prepared the extract and fractions. MMH and MSHK also carried out the study design, performed the experiments, collected and interpreted the data, prepared the manuscript, and performed statistical analysis. MSHK wrote the first draft of the manuscript. MAMD, MSIA, SMZH, RD, and MMNU helped in the experiments, data collection, and literature search. The intermodel relationship idea was uniquely given by MSHK. MMR supervised the study design and data interpretation. All the authors have accepted responsibility for the entire content of the submitted manuscript and approved submission.
Research funding: None declared.
Employment or leadership: None declared.
Honorarium: None declared.
Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.
References
1. Palombo EA. Phytochemicals from traditional medicinal plants used in the treatment of diarrhoea: modes of action and effects on intestinal function. Phytother Res 2006;20:717–24.10.1002/ptr.1907Search in Google Scholar PubMed
2. Banglapedia. Garden flowers. National encyclopedia of Bangladesh (online edition). 2012. Available at: http://www.banglapedia.org/HT/G_0040.htm Accessed 5 June, 2015. ISBN-978-984-512-021-970...978-984-512-048-997.Search in Google Scholar
3. Park K. Park’s textbook of preventive and social medicine. Jabalpur: Banarsidas Bharat Publishers, 2000:122–75.Search in Google Scholar
4. Victora CG, Huttly SR, Fuchs SC, Barros FC, Garenne M, Leroy O, et al. International differences in clinical patterns of diarrhoeal deaths: a comparison of children from Brazil, Senegal, Bangladesh, and India. J Diarrhoeal Dis Res 1993;11:25–9.Search in Google Scholar
5. Das SK, Afroze F, Ahmed T, Faruque AS, Sarker SA, Huq S, et al. Extreme hypernatremic dehydration due to potential sodium intoxication: consequences and management for an infant with diarrhea at an urban intensive care unit in Bangladesh: a case report. J Med Case Rep 2015;9:124.10.1186/s13256-015-0611-ySearch in Google Scholar PubMed PubMed Central
6. Rang HP, Dale MM, Ritter JM, Moore PK. Pharmacology, 5th ed. London: Churchill Livingstone, 2003:375–8.Search in Google Scholar
7. Bustos-Brito C, Sánchez-Castellanos M, Esquivel B, Calderón JS, Calzada F, Yepez-Mulia L, et al. Structure, absolute configuration, and antidiarrheal activity of a thymol derivative from Ageratina cylindrica. J Nat Prod 2014;77:358–63.10.1021/np400964wSearch in Google Scholar PubMed
8. Li J, Wu X-L, Chen Y, Tang Z, Xu Y-H, Jiang J-M, et al. Antidiarrheal properties of different extracts of Chinese herbal medicine formula Bao-Xie-Ning. J Integr Med 2013;11:125–34.10.3736/jintegrmed2013019Search in Google Scholar PubMed
9. Harun-ur-Rashid M, Gafur M, Sadik G, Rahman MA. Biological activities of a new acrylamide derivative from Ipomoea turpithum. Pak J Biol Sci 2002;5:968–9.10.3923/pjbs.2002.968.969Search in Google Scholar
10. Su S, Hua Y, Wang Y, Gu W, Zhou W, Duan J-A, et al. Evaluation of the anti-inflammatory and analgesic properties of individual and combined extracts from Commiphora myrrha, and Boswellia carterii. J Ethnopharmacol 2012;139:649–56.10.1016/j.jep.2011.12.013Search in Google Scholar PubMed
11. Yu C-H, Tang W-Z, Peng C, Sun T, Liu B, Li M, et al. Diuretic, anti-inflammatory, and analgesic activities of the ethanol extract from Cynoglossum lanceolatum. J Ethnopharmacol 2012;139:149–54.10.1016/j.jep.2011.10.031Search in Google Scholar PubMed
12. Wang S, Zhao Y, Zhang J, Huang X, Wang Y, Xu X, et al. Antidiarrheal effect of Alpinia oxyphylla Miq. (Zingiberaceae) in experimental mice and its possible mechanism of action. J Ethnopharmacol 2015;168:182–90.10.1016/j.jep.2015.03.066Search in Google Scholar PubMed
13. Bangladesh Ethnobotany Online Database (BEOD). Phrynium imbricatum Roxb. Available at: http://www.ebbd.info/phrynium-imbricatum.html. Accessed 28 July, 2015.Search in Google Scholar
14. Hossain MM, Kabir MS, Hasanat A, Kabir MI, Chowdhury TA, Kibria AS. Investigation of in vitro anti-arthritic and membrane stabilizing activity of ethanol extracts of three Bangladeshi plants. Pharma Innov 2015;4:76–80.Search in Google Scholar
15. Kabir MS, Dinar MA, Hossain MM, Noman MA, Zaheed F, Hossain MR, et al. Effects of ethanol extract and its different fractions of Phrynium imbricatum (Roxb) leaves on in vitro anthelmintic and their condensed tannin content. Pharm Anal Chem Open Access 2015;1:1–4.Search in Google Scholar
16. Islam MK, Eti IZ, Chowdhury JA. Phytochemical and antimicrobial analysis on the extract of Oroxylum indicum Linn. Stem-Bark. Iranian J Pharmacol Ther 2010;9:25–8.Search in Google Scholar
17. Bulbul IJ, Nahar L, Haque M. Antibacterial, cytotoxic and antioxidant activity of chloroform, n-hexane and ethyl acetate extract of plant Coccinia cordifolia. Agric Biol J N Am 2011;2: 713–9.10.5251/abjna.2011.2.4.713.719Search in Google Scholar
18. Walum E. Acute oral toxicity. Environ Health Perspect 1998;106:497–503.10.1289/ehp.98106497Search in Google Scholar
19. Awouters F, Niemegeers C, Lenaerts F, Janssen P. Delay of castor oil diarrhoea in rats: a new way to evaluate inhibitors of prostaglandin biosynthesis. J Pharm Pharmacol 1978;30:41–5.10.1111/j.2042-7158.1978.tb13150.xSearch in Google Scholar PubMed
20. Robert A, Nezamis J, Lancaster C, Hanchar A, Klepper M. Enteropooling assay: a test for diarrhea produced by prostaglandins. Prostaglandins 1976;11:809–28.10.1016/0090-6980(76)90189-1Search in Google Scholar
21. Mascolo N, Izzo AA, Autore G, Barbato F, Capasso F. Nitric oxide and castor oil-induced diarrhea. J Pharm Exp Ther 1994;268:291–5.10.1016/1043-6618(94)80070-7Search in Google Scholar
22. Koster R, Anderson M, De Beer EJ. Acetic acid-induced analgesic screening. Fed Proc 1959;18:412.Search in Google Scholar
23. Taur DJ, Waghmare MG, Bandal RS, Patil RY. Antinociceptive activity of Ricinus communis L. leaves. Asian Pac J Trop Biomed 2011;1:139–41.10.1016/S2221-1691(11)60012-9Search in Google Scholar
24. Okokon JE, Nwafor PA. Antiinflammatory, analgesic and antipyretic activities of ethanolic root extract of Croton zambesicus. Pak J Pharm Sci 2010;23:385–92.Search in Google Scholar
25. Perez-Gutierrez S, Zavala-Mendoza D, Hernandez-Munive A, Mendoza-Martinez A, Perez-Gonzalez C, Sanchez-Mendoza E. Antidiarrheal activity of 19-deoxyicetexone isolated from Salvia ballotiflora Benth in mice and rats. Molecules 2013;18:8895–905.10.3390/molecules18088895Search in Google Scholar
26. Agbor GA, Leopold T, Jeanne NY. The antidiarrhoeal activity of Alchornea cordifolia leaf extract. Phytother Res 2004;18:873–6.10.1002/ptr.1446Search in Google Scholar
27. Tadesse WT, Hailu AE, Gurmu AE, Mechesso AF. Experimental assessment of antidiarrheal and antisecretory activity of 80% methanolic leaf extract of Zehneria scabra in mice. BMC Complement Altern Med 2014;14:460.10.1186/1472-6882-14-460Search in Google Scholar
28. Rouf AS, Islam MS, Rahman MT. Evaluation of antidiarrhoeal activity Rumex maritimus root. J Ethnopharmacol 2003;84: 307–10.10.1016/S0378-8741(02)00326-4Search in Google Scholar
29. Collier HO, Dinneen LC, Johnson CA, Schneider C. The abdominal constriction response and its suppression by analgesic drugs in the mouse. Br J Pharmacol Chemother 1968;32:295–310.10.1111/j.1476-5381.1968.tb00973.xSearch in Google Scholar
30. Vongtau HO, Abbah J, Ngazal IE, Kunle OF, Chindo BA, Otsapa PB, et al. Anti-nociceptive and anti-inflammatory activities of the methanolic extract of Parinari polyandra stem bark in rats and mice. J Ethnopharmacol 2004;90:115–21.10.1016/j.jep.2003.09.038Search in Google Scholar
31. Ikeda Y, Ueno A, Naraba H, Oh-ishi S. Involvement of vanilloid receptor VR1 and prostanoids in the acid-induced writhing responses of mice. Life Sci 2001;69:2911–9.10.1016/S0024-3205(01)01374-1Search in Google Scholar
32. Choi JH, Jung BH, Kang OH, Choi HJ, Park PS, Cho SH, et al. The anti-inflammatory and anti-nociceptive effects of ethyl acetate fraction of cynanchi paniculati radix. Biol Pharm Bull 2006;29:971–5.10.1248/bpb.29.971Search in Google Scholar PubMed
33. Serhan CN, Haeggstrom JZ. Lipid mediators in acute inflammation and resolution: eicosanoids, PAF, resolvins, and protectins. In: Fundamentals of inflammation. Cambridge, UK: Cambridge University Press, 2010;26:153–74.10.1017/CBO9781139195737.014Search in Google Scholar
34. Deraedt R, Jouquey S, Delevallee F, Flahaut M. Release of prostaglandins E and F in an algogenic reaction and its inhibition. Eur J Pharmacol 1980;61:17–24.10.1016/0014-2999(80)90377-5Search in Google Scholar
35. Millan MJ. The induction of pain: an integrative review. Prog Neurobiol 1999;57:1–164.10.1016/S0301-0082(98)00048-3Search in Google Scholar
36. Dubuisson D, Dennis SG. The formalin test: a quantitative study of the analgesic effects of morphine, meperidine, and brain stem stimulation in rats and cats. Pain 1977;4:161–74.10.1016/0304-3959(77)90130-0Search in Google Scholar
37. Heapy CG. Afferent C-fiber and A-delta activity in models of inflammation. Br J Pharmacol 1987;90:164.Search in Google Scholar
38. Malmberg AB, Yaksh TL. Antinociceptive actions of spinal nonsteroidal anti-inflammatory agents on the formalin test in the rat. J Pharmacol Exp Ther 1992;263:136–46.10.1016/S0022-3565(25)10314-5Search in Google Scholar
39. Verma PR, Joharapurkar AA, Chatpalliwar VA, Asnani AJ. Antinociceptive activity of alcoholic extract of Hemidesmus indicus R.Br. in mice. J Ethnopharmacol 2005;102:298–301.10.1016/j.jep.2005.05.039Search in Google Scholar PubMed
40. Tang L, Chen Y, Chen Z, Blumberg PM, Kozikowski AP, Wang ZJ. Antinociceptive pharmacology of N-(4-chlorobenzyl)-N′-(4-hydroxy-3-iodo-5-methoxybenzyl) thiourea, a high-affinity competitive antagonist of the transient receptor potential vanilloid 1 receptor. J Pharmacol Exp Ther 2007;321:791–8.10.1124/jpet.106.117572Search in Google Scholar PubMed
41. Sani MH, Zakaria ZA, Balan T, Teh LK, Salleh MZ. Antinociceptive activity of methanol extract of Muntingia calabura leaves and the mechanisms of action involved. Evid Based Complement Alternat Med 2012;890361:26.10.1155/2012/890361Search in Google Scholar
©2017 Walter de Gruyter GmbH, Berlin/Boston
Articles in the same Issue
- Frontmatter
- Review
- Natural product for the treatment of Alzheimer’s disease
- Behavior and Neuroprotection
- Evidence for the involvement of the GABA-ergic pathway in the anticonvulsant activity of the roots bark aqueous extract of Anthocleista djalonensis A. Chev. (Loganiaceae)
- Cardiovascular Function
- Cutaneous temperature sensitivity alteration in subjects with chronic stroke sequelae – pharmacological perspectives
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- Phytotherapy
- Antidiarrheal and antinociceptive activities of ethanol extract and its chloroform and pet ether fraction of Phrynium imbricatum (Roxb.) leaves in mice
- Amelioration of hyperglycemia and associated metabolic abnormalities by a combination of fenugreek (Trigonella foenum-graecum) seeds and onion (Allium cepa) in experimental diabetes
- An ethanolic extract of Desmodium adscendens exhibits antipsychotic-like activity in mice
Articles in the same Issue
- Frontmatter
- Review
- Natural product for the treatment of Alzheimer’s disease
- Behavior and Neuroprotection
- Evidence for the involvement of the GABA-ergic pathway in the anticonvulsant activity of the roots bark aqueous extract of Anthocleista djalonensis A. Chev. (Loganiaceae)
- Cardiovascular Function
- Cutaneous temperature sensitivity alteration in subjects with chronic stroke sequelae – pharmacological perspectives
- Combinatorial therapy of exercise-preconditioning and nanocurcumin formulation supplementation improves cardiac adaptation under hypobaric hypoxia
- Oxidative Stress
- Phellinus rimosus improves mitochondrial energy status and attenuates nephrotoxicity in diabetic rats
- Hepatoprotective effects of Vaccinium arctostaphylos against CCl4-induced acute liver injury in rats
- The impact of vitamin C on the relationship among inflammation, lipid peroxidation and platelet activation during analgesic nephropathy in rats
- Phytotherapy
- Antidiarrheal and antinociceptive activities of ethanol extract and its chloroform and pet ether fraction of Phrynium imbricatum (Roxb.) leaves in mice
- Amelioration of hyperglycemia and associated metabolic abnormalities by a combination of fenugreek (Trigonella foenum-graecum) seeds and onion (Allium cepa) in experimental diabetes
- An ethanolic extract of Desmodium adscendens exhibits antipsychotic-like activity in mice