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氢溴酸槟榔碱体内对大鼠肝肾转运体表达的影响
引用本文:翟婷,黄祥涛,王俊俊,陈勇.氢溴酸槟榔碱体内对大鼠肝肾转运体表达的影响[J].中草药,2017,48(13):2711-2716.
作者姓名:翟婷  黄祥涛  王俊俊  陈勇
作者单位:湖北大学 中药生物技术省重点实验室, 湖北大学生物资源绿色转化协同创新中心, 湖北 武汉 430062;湖北大学 中药生物技术省重点实验室, 湖北大学生物资源绿色转化协同创新中心, 湖北 武汉 430062;湖北大学 中药生物技术省重点实验室, 湖北大学生物资源绿色转化协同创新中心, 湖北 武汉 430062;湖北大学 中药生物技术省重点实验室, 湖北大学生物资源绿色转化协同创新中心, 湖北 武汉 430062
基金项目:教育部大学生创新创业训练计划项目(201410512010)
摘    要:目的探究氢溴酸槟榔碱对大鼠肝肾转运体表达的影响。方法通过给雄性Wistar大鼠ig氢溴酸槟榔碱(0.8、4、20 mg/kg)21 d,应用荧光RT-PCR检测肝、肾组织中13种转运体m RNA的表达量,考察氢溴酸槟榔碱对大鼠肝、肾转运体m RNA表达的影响。结果氢溴酸槟榔碱低剂量时显著抑制了肝脏MRP2和MDR1A m RNA表达,但显著诱导了肾脏MRP5 m RNA表达。氢溴酸槟榔碱高剂量时显著抑制了肝脏OCT2、OAT2、OCTN2、OATP1A1、OATP1A4、OATP2B1、MRP2和MDR1A,以及肾脏MRP2、BCRP、MDR1A的m RNA表达水平,但显著上调了肾脏OCTN2、OATP1A1、OATP1A4及MRP5的m RNA表达量,且对上述转运体m RNA表达的影响有一定剂量依赖性。结论由于肝肾转运体表达与功能的改变会引起药物相互作用,临床上应给予槟榔嗜好者更多关注,以避免发生不良药物相互作用。

关 键 词:氢溴酸槟榔碱  药物转运体  药物相互作用  MRP2  MDR1A  OATP1A4  OCTN2
收稿时间:2016/12/19 0:00:00

Effect of arecoline hydrobromide on mRNA expression of hepatic and renal transporters in vivo
ZHAI Ting,HUANG Xiang-tao,WANG Jun-jun and CHEN Yong.Effect of arecoline hydrobromide on mRNA expression of hepatic and renal transporters in vivo[J].Chinese Traditional and Herbal Drugs,2017,48(13):2711-2716.
Authors:ZHAI Ting  HUANG Xiang-tao  WANG Jun-jun and CHEN Yong
Institution:Hubei Province Key Laboratory of Biotechnology of Chinese Traditional Medicine, Hubei Collaborative Innovation Center for Green Transformation of Bio-resources, Hubei University, Wuhan 430062, China;Hubei Province Key Laboratory of Biotechnology of Chinese Traditional Medicine, Hubei Collaborative Innovation Center for Green Transformation of Bio-resources, Hubei University, Wuhan 430062, China;Hubei Province Key Laboratory of Biotechnology of Chinese Traditional Medicine, Hubei Collaborative Innovation Center for Green Transformation of Bio-resources, Hubei University, Wuhan 430062, China;Hubei Province Key Laboratory of Biotechnology of Chinese Traditional Medicine, Hubei Collaborative Innovation Center for Green Transformation of Bio-resources, Hubei University, Wuhan 430062, China
Abstract:Objective To investigate the protective effect of ginseng fruit anthocyanins (GFA) against acetaminophen (AP) induced liver damage in mice and its possible mechanism. Methods The model of AP induced liver injury was established, and the GFA protection for liver damage was observed. Thirty-two male ICR mice were randomly divided into normal group, AP group, GFA with 200 mg/kg dose group, and GFA with 400 mg/kg group. Colorimetric method was used to assay the contents of serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST), activity of glutathione (GSH) and malondialdehyde (MDA) content of liver homogenate in mice, and observe liver tissue pathological section. Results GFA obviously reduced the level of ALT in serum, inhibited the level of MDA, and enhanced activity of GSH in liver tissue. The H&E and Hoechst 33258 staining results indicated that GFA could obviously improve the degree of liver tissue necrosis and apoptosis, narrow the scope of necrosis, and relieve the inflammatory cell infiltration. By inflammatory factor of iNOS, COX-2 immunohistochemical staining and nitrification stress index of 3-NT immunofluorescence, GFA could inhibit nitration stress and the expression of inflammatory cytokines. Conclusion GFA has certain protective effect on AP-induced acute liver injury and its mechanism may relate to antioxidant effect, inhibition of nitrification stress, alleviation inflammation reaction and inhibiting apoptosis.
Keywords:arecoline hydrobromide  drug transporter  drug interaction  MRP2  MDR1A  OATP1A4  OCTN2
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