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. 2024 Dec 12;22(4):15593258241308998. doi: 10.1177/15593258241308998

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© The Author(s) 2024

This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).

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Figure 3. — The rats (n = 6) were treated with 250 and 500 mg/kg of n-hexane extract of A. nilotica pods (ANPH) and methanol extract of A. nilotica (ANPM) for 2 weeks followed by administration of a toxic dose of paracetamol (PCM). The hepatoprotective potential of both extracts was assessed by monitoring the (A) bilirubin, (B) ALP, (C) ALT and (D) AST levels. The data are presented as mean ± SD and evaluated by one-way ANOVA followed by Tukey’s test. The *P < 0.05, **P < 0.01, ***P < 0.001 and ****P < 0.0001 were considered statistically significant in comparison with the PCM-treated rats while ns shows non-significant outcomes. ALP: alkaline phosphatase; ALT: alanine transaminase also known as SGPT: serum glutamate pyruvate transaminase; AST: aspartate aminotransferase also known as SGOT: glutamic-oxaloacetic transaminase.