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Effect of Olea oleaster and Juniperus procera leaves extracts on thioacetamide induced hepatic cirrhosis in male albino mice

机译:油橄榄和刺柏叶提取物对硫代乙酰胺诱导的雄性白化病小鼠肝硬化的影响

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摘要

The effect of Olea oleaster and Juniperus procera leaves extracts and their combination on thioacetamide (TAA)-induced hepatic cirrhosis were investigated in male albino mice. One hundred sixty mice were used in this study and were randomly distributed into eight groups of 20 each. Mice of group 1 served as controls. Mice of group 2 were treated with TAA. Mice of group 3 were exposed to TAA and supplemented with O. oleaster leaves extracts. Mice of group 4 were treated with TAA and supplemented with J. procera leaves extracts. Mice of group 5 were subjected to TAA and supplemented with O. oleaster and J. procera leaves extracts. Mice of groups 6, 7 and 8 were supplemented with O. oleaster, J. procera, and O. oleaster and J. procera leaves extracts respectively. Administration of TAA for six and twelve weeks resulted in a decline in body weight gain and increased the levels of serum alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase and total bilirubin. Histopathological evaluations of hepatic sections from mice treated with TAA showed severe alterations including increase of fibrogenesis processes with structural damage. Treatment of mice with these extracts showed a pronounced attenuation in TAA induced hepatic cirrhosis associated with physiological and histopathological alterations. Finally, this study suggests that the supplementation of these extracts may act as antioxidant agents and could be an excellent adjuvant support in the therapy of hepatic cirrhosis.
机译:在雄性白化病小鼠中,研究了油橄榄(Olea oleaster)和杜鹃(Juniperus procera)叶提取物及其组合对硫代乙酰胺(TAA)诱导的肝硬化的影响。这项研究使用了一百六十只小鼠,随机分为八组,每组二十只。第1组的小鼠用作对照。组2的小鼠用TAA治疗。将第3组的小鼠暴露于TAA并补充O.oleaster叶提取物。用TAA处理第4组的小鼠,并补充J.procera叶提取物。对第5组的小鼠进行TAA,并补充O.oleaster和J.procera叶提取物。第6、7和8组的小鼠补充了O. oleaster,J。procera,O。oleaster和 J procera 分别提取提取物。服用TAA 6周和12周会导致体重增加减少,并增加血清丙氨酸氨基转移酶,天冬氨酸氨基转移酶,碱性磷酸酶和总胆红素的水平。用TAA处理的小鼠肝脏切片的组织病理学评估显示,严重的改变包括纤维化过程的增加以及结构性损伤。用这些提取物治疗小鼠后,TAA诱发的肝硬化明显减弱,并伴有生理和组织病理学改变。最后,这项研究表明,这些提取物的补充可作为抗氧化剂,并可能在肝硬化的治疗中提供出色的佐剂支持。

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