Benedict Bolakponumigha Iwetan1,
Godfrey Rume Kweki2 ,
Divine A Onobrudu2,
Uzuegbu Ugochukwu2,
Ohwokevwo Oghenenyore Andy3,
Lawrence Oberhiri Ewhre1,
Atuboyedia Wolfe Obianime4
For correspondence:- Godfrey Kweki Email: kweki.godfrey@delsu.edu.ng Tel:+234-7034331346
Received: 6 March 2025 Accepted: 22 May 2025 Published: 31 May 2025
Citation: Iwetan BB, Kweki GR, Onobrudu DA, Ugochukwu U, Andy OO, Ewhre LO, et al. Hepatorenal protection of Justicia carnea leaf aqueous extract on sheep red blood cell-induced immunotoxicity in mice. Trop J Pharm Res 2025; 24(5):667-676 doi: https://dx.doi.org/10.4314/tjpr.v24i5.5
© 2025 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..
Purpose: To evaluate the hepatorenal protective properties of Justicia carnea (Acanthaceae) aqueous leaf extract against Sheep Red Blood Cells (SRBC)-induced immunotoxicity in mice. Method: Thirty-six (36) male mice were randomly selected into six groups of six mice each. Group I (VEH control) was administered distilled water only, while Groups II – VI mice were immunized intraperitoneally with SRBC (0.2 mL/kg) on days 1 and 5. In addition, Groups III – V were given 125, 250 and 500 mg/kg of JC aqueous extract, respectively and Levamisole (LEV; 7.5 mg/kg) was administered to mice in Group VI. From days 3 to 9, the mice received daily oral doses of their assigned treatment agents. On day 10, the animals were sacrificed, and blood, liver, and kidney tissues were collected for biochemical analysis. Result: There were significant changes in Aspartate Transferase (AST), Alanine Transferase (ALT), Alkaline Phosphatase (ALP) and Albumin (ALB) levels of SRBC-induced mice (p < 0.05), which were reversed almost to the baseline value of VEH group. However, at JC 250 and 500 mg/kg, there was a significant increase in total protein (TP) level compared to VEH, LEV and SRBC groups (p < 0.05). Aqueous JC extract significantly reduced the increased urea concentration induced by SRBC, though not to baseline, compared to LEV (p < 0.05). Also, the extract significantly altered activities of oxidative enzymes such as aldehyde oxidase (AO), monoamine oxidase (MAO) and peroxidase (PO) compared to control (p < 0.05). Conclusion: Justicia carnea significantly restores liver and kidney functions in mice treated with SRBCs, comparable to levamisole. These findings unveil the potential of J. carnea leaf extract as an adjuvant in vaccine therapy
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