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Original Research Article | OPEN ACCESS

Hepatoprotective and antioxidant properties of the methanol leaf extract of Diaphananthe bidens in acetaminophen-induced hepatotoxicity in rats

Patrick E Aba1, Kenneth O Ugwueze1, Samuel O Onoja2 , Christian O Okorie-Kanu3, Aruh O Anaga1

1Department of Veterinary Physiology and Pharmacology, University of Nigeria, Nsukka; 2Department of Veterinary Physiology and Pharmacology; 3Department of Veterinary Pathology, Michael Okpara University of Agriculture, Umudike, Nigeria.

For correspondence:-  Samuel Onoja   Email: onoja.samuel@mouau.edu.ng

Accepted: 17 October 2019        Published: 30 November 2019

Citation: Aba PE, Ugwueze KO, Onoja SO, Okorie-Kanu CO, Anaga AO. Hepatoprotective and antioxidant properties of the methanol leaf extract of Diaphananthe bidens in acetaminophen-induced hepatotoxicity in rats. Trop J Pharm Res 2019; 18(11):2371-2377 doi: 10.4314/tjpr.v18i11.20

© 2019 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: To investigate the hepatoprotective and antioxidant properties of the methanol extract of Diaphananthe bidens leaf using acetaminophen-induced hepatotoxicity rat model.
Methods: Thirty albino Wistar rats, randomly assigned into 6 groups (A - F, n = 5), were used for the study. Groups A and B received distilled water (10 ml/kg), group C received silymarin (0.10 g/kg) while groups D - F received D. bidens extract 0.15, 0.30 and 0.60 g/kg, respectively, for 7 days. On day 8, groups B - F rats received acetaminophen (2 g/kg) orally. About 48 h later, pentobarbitone sodium (0.035 g/kg) was injected intraperitoneally for sleeping time studies. The time of sleep, time of awake and the duration of sleep were recorded. On awakening, blood samples were collected for evaluation of serum biochemical parameters and antioxidant profile. Thereafter, the rats were humanely euthanized and the liver excised for histopathological evaluation. In vitro antioxidant activity of the extract was evaluated using ferric reducing antioxidant power and 2,2-diphenyl-1-picrylhydrazine (DPPH) scavenging assay. 
Results: Treatment of the rats with D. bidens decreased (p < 0.05) malondialdehyde values and activities of ALT, AST and ALP, but increased glutathione levels and catalase activities when compared to negative control group. The extract significantly (p < 0.05) decreased sodium pentobarbitone-induced sleeping time relative to the negative control group and produced concentration-dependent increase in antioxidant activities in vitro. The extract protected the hepatocyte against acetaminophen-induced damage.
Conclusion: D. bidens extract elicits antioxidant activities in vitro and in vivo and thus, protects rat liver against acetaminophen-induced damage. Therefore, the extract can potentially be developed as a hepatoprotective agent for the clinical management of liver damage.

Keywords: Diaphananthe bidens, Hepatoprotection, Antioxidant; Histopathology, Biochemical parameters

Impact Factor
Thompson Reuters (ISI): 0.523 (2021)
H-5 index (Google Scholar): 39 (2021)

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