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LPS下调小鼠肝脏、肠道羧酸酯酶表达
  • 期刊名称:现代生物医学进展。2010,10(6):1030-33。
  • 时间:0
  • 分类:Q95-3[生物学—动物学] Q593[生物学—生物化学]
  • 作者机构:[1]南京医科大学药理学系,江苏南京210029
  • 相关基金:国家自然科学基金资助项目(No.30772616)
  • 相关项目:在对IL6的反应中DEC1负性调节肝脏药物代谢酶CYP3A4表达
中文摘要:

目的:研究细菌脂多糖(LPS)对小鼠肝脏、肠道羧酸酯酶表达及酶活性的影响。方法:小鼠经腹腔注射5.0mg/kg的LPS,对照组给予生理盐水。注射后24h处死小鼠,取肝脏和肠道组织。用qRT—PCR技术检测小鼠肝脏、肠道组织羧酸酯酶1和2(mCES1和mCES2)mRNA水平;Westernblot技术检测小鼠肝脏、肠道组织mCES1和mCES2蛋白表达水平。用分光光度计检测小鼠肝脏、肠道组织羧酸酯酶总活性。结果:LPS显著降低小鼠肝脏、肠道组织羧酸酯酶1和2的mRNA水平(P〈0.05),同时LPS也显著降低小鼠肝脏、肠道组织羧酸酯酶的蛋白表达水平及酶活性(P〈0.05)。结论:LPS造成的炎症状态可显著降低小鼠肝脏、肠道组织羧酸酯酶的表达及酶活性。

英文摘要:

Objective: To investigate the effects of lipopolysaccharide (LPS) on the expressions of carboxylesterasel and 2 in mouse liver and intestine. Methods: All mice except controls received an intraperitoneal injection ofLPS 5.0mg / kg. The mice were sacrificed at 24h aRer LPS treatment. Liver and Intestine carboxylesterasel and 2 mRNA were determined by real-time PCR. Carboxylesterase activities was measured by the para-nitrophenylacetate reagent. Liver and Intestine carboxylesterasel and 2 protein levels were determined by Western Blot. Results: LPS not only inhibited the expressions of liver carboxylesterasel and 2, but also down-regulated the levels of carboxylesterase 1 and 2 of intestine. Furthermore, LPS repressed the carboxylesterase catalytic activity in mice livers and intestines. Conclusions: LPS suppresses the expressions of carboxylesterase 1 and 2 in mouse liver and intestine.

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