Suppr超能文献

中枢血管紧张素II受体介导对应激源的血流动力学反应变异性。

Central angiotensin II receptors mediate hemodynamic response variability to stressors.

作者信息

Rowe Kayla D, Schwartz Julie A, Lomax Lance L, Knuepfer Mark M

机构信息

Dept. of Pharmacological and Physiological Science, St. Louis University School of Medicine, St. Louis, MO 63104, USA.

出版信息

Am J Physiol Regul Integr Comp Physiol. 2006 Sep;291(3):R719-27. doi: 10.1152/ajpregu.00825.2005. Epub 2006 Apr 6.

Abstract

We examined whether ANG II receptors in the central nervous system mediate hemodynamic responses to pharmacological (cocaine) and behavioral (cold water) stressors. After administration of cocaine (5 mg/kg iv), rats were classified as vascular responders (VR) if their pressor response was due entirely to an increase in systemic vascular resistance (SVR) despite a decrease in cardiac output (CO). Cocaine elicited a pressor response in mixed responders (MR) that was dependent on small increases in both SVR and CO. ANG II (30 ng/5 microl icv, 5 min before cocaine) augmented the decrease in CO in VR and prevented the increase in CO in MR. Administration of [Sar(1),Thr(8)]ANG II (20 microg/5 microl icv; sarthran) before cocaine attenuated the decrease in CO and the large increase in SVR in VR so that they were no longer different from MR. Losartan (20 microg icv) or captopril (50 microg icv) preceding cocaine administration also attenuated the decrease in CO and the large increase in SVR seen in VR only. The role of angiotensin was not specific for cocaine, because ANG II (icv) pretreatment before startle with cold water (1 cm deep) enhanced the decrease in CO and the increase in SVR in both MR and VR, whereas losartan (icv) pretreatment before startle attenuated the decrease in CO and the increase in SVR in VR so that they were no longer different from MR. These data suggest that central ANG II receptors mediate the greater vascular and cardiac responsiveness in vascular responders to acute pharmacological and behavioral stressors.

摘要

我们研究了中枢神经系统中的血管紧张素II(ANG II)受体是否介导对药理学(可卡因)和行为学(冷水)应激源的血液动力学反应。静脉注射可卡因(5毫克/千克)后,若大鼠的升压反应完全归因于全身血管阻力(SVR)增加而心输出量(CO)减少,则将其归类为血管反应者(VR)。可卡因在混合反应者(MR)中引发的升压反应依赖于SVR和CO的小幅增加。ANG II(30纳克/5微升,脑室内注射,在注射可卡因前5分钟)增强了VR中CO的降低,并阻止了MR中CO的增加。在注射可卡因前给予[Sar(1),Thr(8)]ANG II(20微克/5微升;沙坦)减弱了VR中CO的降低和SVR的大幅增加,使其与MR不再有差异。在注射可卡因前给予氯沙坦(20微克,脑室内注射)或卡托普利(50微克,脑室内注射)也仅减弱了VR中可见的CO降低和SVR大幅增加。血管紧张素的作用并非可卡因所特有,因为在冷水(1厘米深)惊吓前进行ANG II(脑室内注射)预处理增强了MR和VR中CO的降低以及SVR的增加,而在惊吓前进行氯沙坦(脑室内注射)预处理减弱了VR中CO的降低和SVR的增加,使其与MR不再有差异。这些数据表明,中枢ANG II受体介导了血管反应者对急性药理学和行为学应激源的更大血管和心脏反应性。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验