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首页|期刊导航|中国药理学通报|mmLDL对小鼠肠系膜动脉α1受体介导的血管收缩及相关蛋白表达影响的研究

mmLDL对小鼠肠系膜动脉α1受体介导的血管收缩及相关蛋白表达影响的研究

郭立军 江高峰 李海鹏 李琼 刘恩岐 李洁

中国药理学通报Issue(6):827-832,833,7.
中国药理学通报Issue(6):827-832,833,7.DOI:10.3969/j.issn.1001-1978.2015.06.018

mmLDL对小鼠肠系膜动脉α1受体介导的血管收缩及相关蛋白表达影响的研究

Study of α1 adrenoceptor-mediated vasoconstriction and protein expressions induced by mmLDL in mouse mesenteric artery

郭立军 1江高峰 2李海鹏 3李琼 1刘恩岐 1李洁4

作者信息

  • 1. 南华大学附属郴州市第一人民医院,湖南 郴州 423000
  • 2. 湘南学院,湖南 郴州 423000
  • 3. 南华大学药物药理研究所,湖南 衡阳 421001
  • 4. 西安交通大学医学院实验动物中心,陕西 西安 710061
  • 折叠

摘要

Abstract

Aim To investigate the effects of mmLDL on the up-regulation ofα1 receptors in moues mesenter- <br> ic arteries. Methods Mice tail intravenous injection of mmLDL was used . Vitro sensitive myograph was empl- <br> oyed to examine Noradrenaline ( NA) induced vascular contraction on mice mesenteric artery, and the mRNA and protein expressions ofα1 andα2 receptors were an-alyzed by real-time PCR and Western blot, respective-ly. Results mmLDL significantly increased NA in-duced concentration-contractile curve, and the data of Emax and pEC50 were from ( 122. 61 ± 9. 40 )% and (5. 65 ± 0. 05 ) in normal saline ( NS ) group to (161. 01 ± 6. 90 )% and ( 6. 20 ± 0. 08 ) in mmLDL group (P <0. 01, P <0. 01), respectively. The α1 adrenoceptor antagonist prazosin shifted the concentra- <br> tion-contractile curve induced by NA towards right. Af-ter using mmLDL, the mRNA and protein levels of α1 adrenoceptor were significantly increased, but the mR-NA and protein levels of α2 adrenoceptor were not changed. Conclusion Tail intravenous injection of mmLDL enhances the vascular expressions of α1 adre-noceptors and the contractile effects mediated byα1 ad-renoceptors.

关键词

mmLDL/肠系膜动脉/α1 受体/哌唑嗪/育亨宾/尾静脉注射

Key words

mmLDL/mesenteric artery/α1 adreno-ceptor/prazosin/yohimbine/tail intravenous injection

分类

医药卫生

引用本文复制引用

郭立军,江高峰,李海鹏,李琼,刘恩岐,李洁..mmLDL对小鼠肠系膜动脉α1受体介导的血管收缩及相关蛋白表达影响的研究[J].中国药理学通报,2015,(6):827-832,833,7.

基金项目

国家自然科学基金资助项目( No 81202535) ( No 81202535)

郴州市科技局资助项目(No CZ2014015) (No CZ2014015)

中国药理学通报

OA北大核心CSCDCSTPCD

1001-1978

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