Modulatory effect of Prosopis juliflora leaves on hepatic fibrogenic and fibrolytic alterations induced in rats by thioacetamide - 09/06/19


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Graphical abstract |
Highlights |
• | PJEL extract is rich in polyphenolic flavones and alkaloids. |
• | PJEL showed strong free radical activity. |
• | PJEL possessed cytotoxic activity against HepG2 cell line (IC50 = 11.1 μg/ml). |
• | PJEL enhanced extracellular matrix removal. |
• | PJEL stimulates hepatic regeneration to decrease hepatic necrosis. |
Abstract |
This study investigated the antifibrotic effect of Prosopis juliflora leaves crude methanolic extract (PJEL) against thioacetamide (TAA)-induced liver fibrosis. The phytochemical analysis of PJEL was performed via HPLC/MS in association with evaluating its free radical scavenging and cytotoxic activities. The antifibrotic activity of PJEL was assessed by dividing Wistar rats into 8 groups: normal control, PJEL1-administered rats (2 mg/ Kg b.w.), PJEL2-administered rats (4 mg/ Kg b.w.), PJEL3-administered rats (8 mg/Kg b.w.), TAA-induced hepatic fibrosis, TTA + PJEL1, TAA + PJEL2, and TAA + PJEL3. Results indicated that PJEL crude methanolic extract is rich in polyphenolic compounds and alkaloids. PJEL exerted free radical scavenging activity with IC50 of 123.5 μg/mL and cytotoxic activity against a well-differentiated hepatocellular cell line (IC50 = 11.1 μg/mL). PJEL at a dose of 4 mg/Kg b.w. ameliorated serum ALT activity and improved serum albumin level and hepatic hydroxyproline content in association with a reduction in the fibrosis stage. PJEL elevated hepatic tumor necrosis factor-α and interleukin-6 contents with less necrosis grade. PJEL post-therapy ameliorated the relative expression of Bcl-2, Col1A1, Mmp-9, and Mmp-2 genes in liver.
Conclusion |
PJEL possesses a good therapeutic activity against TAA-induced liver fibrosis via enhancing extracellular matrix removal and stimulating hepatic regeneration to decrease hepatic necrosis.
Le texte complet de cet article est disponible en PDF.Keywords : Fibrosis, Necrosis, Extracellular matrix removal, Regeneration
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Vol 115
Article 108788- juillet 2019 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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