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微量氨基酸相关受体激活剂在隔离的透气小鼠脏中的血管收缩作用
Dina Jragh1, Mariam H M Yousif1, Mabayoje A Oriowo1
1Department of Pharmacology and Toxicology, College of Medicine, Kuwait University, Kuwait City, Kuwait.
概括
微量胺相关受体 (TAARs) 的激活会通过细胞外流入和敏感化引起脏血管收缩. 在自发高血压的老鼠中,反应性氧物种也对这种TAAR介导的效应作出了贡献.
科学领域:
- 药理学 药理学是指药理学的学科.
- 腎臟病學 (nephrology) 是一種醫學專業.
- 身体生理学 身体生理学
背景情况:
- 内源性微量胺,如胺和3-氨胺 (T1AM),存在于哺乳动物组织中.
- 这些胺通过激活微量胺相关受体 (TAARs) 产生作用,这些受体是G蛋白结合的受体.
研究的目的:
- 为了研究三胺,T1AM和选择性TAAR1激动剂 (RO5263397) 的血管收缩作用,在孤立的透的老鼠脏中.
- 阐明TAAR介导的血管收缩的潜在机制.
主要方法:
- 使用Wistar Kyoto (WKY) 和自发高血压大鼠 (SHRs) 隔离的透过的老鼠模型.
- 用激动剂和抗剂进行剂量反应实验 (EPPTB).
- 评估通道,Rho-酶,蛋白酶C (PKC) 和活性氧物种 (ROS) 的参与.
主要成果:
- 三胺,T1AM和RO5263397诱导了WKY和SHR脏的输液压的剂量依赖性增加.
- 通过对抗剂EPPTB.的TAAR1激活得到证实.
- 血管收缩涉及细胞外流入,增强敏感性和ROS (在SHR中).
结论:
- TAAR的激活导致脏血管收缩.
- 这些机制涉及细胞外,敏感化和ROS,特别是在SHR中.
- TAARs在调节血管度方面发挥着重要作用.
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