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坎地沙坦与血管紧张素-(1-7)联合治疗对 (mREN2)27 大鼠血压和交感神经-迷走神经平衡的影响比较。

Comparison of Candesartan and Angiotensin-(1-7) Combination to Mito-TEMPO Treatment for Normalizing Blood Pressure and Sympathovagal Balance in (mREN2)27 Rats.

机构信息

Hypertension & Vascular Research, Cardiovascular Sciences Center, Wake Forest University School of Medicine, Winston-Salem, NC.

General Surgery, Wake Forest University School of Medicine, Winston-Salem, NC.

出版信息

J Cardiovasc Pharmacol. 2019 Mar;73(3):143-148. doi: 10.1097/FJC.0000000000000645.

Abstract

Hypertensive transgenic (mRen2)27 rats exhibit impaired baroreflex sensitivity (BRS) for control of heart rate (HR). Intracerebroventricular infusion of Ang-(1-7) improves indices of vagal BRS independent of lowering mean arterial pressure (MAP), whereas AT1 receptor blockade normalizes MAP and indices of sympathetic tone without correcting the vagal BRS. Scavenging cellular reactive oxygen species (ROS) with tempol in brain fails to correct either hypertension or sympathovagal balance in these animals, despite reports that mitochondrial ROS contributes to Ang II-infusion hypertension. To examine effects of a putative preferential mitochondrial ROS scavenger in the brain of (mRen2)27 rats, ICV infusions of Mito-TEMPO (3.2 μg/2.5 μL/h) were compared with artificial cerebrospinal fluid (aCSF; 2.5 μL/h) and combination AT1 receptor antagonist candesartan (CAN: 4 μg/2.5 μL/h) plus Ang-(1-7) (0.1 μg/2.5 μL/h) treatment. MAP was lower after CAN + Ang-(1-7) treatment, and both vagal and sympathetic components of BRS and sympathovagal balance were improved. By contrast, Mito-TEMPO improved sympathetic components of BRS and tended to improve overall sympathovagal balance but failed to alter MAP in this model of hypertension. Although further studies are required to determine whether Mito-TEMPO or CAN + Ang-(1-7) treatment at the doses used altered mitochondrial ROS, optimal therapeutic benefits are achieved by shifting the balance from Ang II toward Ang-(1-7) in this model of chronic RAS-dependent hypertension.

摘要

高血压转基因(mRen2)27 大鼠表现出心率(HR)控制的压力反射敏感性(BRS)受损。脑室内输注 Ang-(1-7)可改善迷走神经 BRS 的指数,而不降低平均动脉压(MAP),而 AT1 受体阻断可正常化 MAP 和交感神经张力指数,而不纠正迷走神经 BRS。用tempo 在大脑中清除细胞活性氧物质(ROS)并不能纠正这些动物的高血压或交感神经平衡,尽管有报道称线粒体 ROS 有助于 Ang II 输注性高血压。为了研究脑内一种假定的线粒体 ROS 清除剂对(mRen2)27 大鼠的影响,比较了脑室内输注 Mito-TEMPO(3.2 μg/2.5 μL/h)与人工脑脊液(aCSF;2.5 μL/h)以及组合 AT1 受体拮抗剂坎地沙坦(CAN:4 μg/2.5 μL/h)加 Ang-(1-7)(0.1 μg/2.5 μL/h)治疗的效果。CAN+Ang-(1-7)治疗后 MAP 降低,BRS 的迷走神经和交感神经成分以及交感神经平衡均得到改善。相比之下,Mito-TEMPO 改善了 BRS 的交感神经成分,并且倾向于改善整体交感神经平衡,但在这种高血压模型中不能改变 MAP。尽管需要进一步研究来确定在这种剂量下使用的 Mito-TEMPO 或 CAN+Ang-(1-7)治疗是否改变了线粒体 ROS,但在这种慢性 RAS 依赖性高血压模型中,通过将平衡从 Ang II 转移到 Ang-(1-7)可以实现最佳的治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf56/8427515/a4f2715a6031/nihms-1044223-f0001.jpg

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Evidence for a mitochondrial angiotensin-(1-7) system in the kidney.肾脏中线粒体血管紧张素 -(1 - 7)系统的证据。
Am J Physiol Renal Physiol. 2016 Apr 1;310(7):F637-F645. doi: 10.1152/ajprenal.00479.2015. Epub 2015 Dec 23.
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Genetic disorders coupled to ROS deficiency.与活性氧缺乏相关的遗传疾病。
Redox Biol. 2015 Dec;6:135-156. doi: 10.1016/j.redox.2015.07.009. Epub 2015 Jul 17.

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