在去卵巢大鼠中,补充雌二醇或诱导高血压可能会减弱血管紧张素II型受体拮抗剂促进肾血流对血管紧张素II分级给药的反应。

IF 2.1 4区 医学 Q3 PERIPHERAL VASCULAR DISEASE
Journal of the Renin-Angiotensin-Aldosterone System Pub Date : 2022-07-01 eCollection Date: 2022-01-01 DOI:10.1155/2022/3223008
Samira Choopani, Mehdi Nematbakhsh
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引用次数: 1

摘要

背景:雌激素替代疗法(ERT)和高血压可能影响女性肾素-血管紧张素系统(RAS)及其组分。血管紧张素II (Ang II) 1型受体(AT1R)拮抗剂(氯沙坦)可促进肾血流量(RBF),在临床上被广泛用于控制高血压。本研究的主要目的是雌二醇或诱导高血压对氯沙坦治疗的去卵巢(OVX)大鼠RBF对Ang II反应的影响。方法:两组OVX大鼠分别给予安慰剂(1组)和雌二醇(2组)治疗4周,另一组OVX大鼠采用两肾一clip (2K1C)模型诱导高血压(3组)。所有组均在麻醉下进行手术,并用氯沙坦阻断AT1R。测定并比较Angⅱ给药后RBF和肾血管阻力(RVR)的反应。结果:3组平均动脉压(MAP)、肾灌注压(RPP)、2组子宫重(UT)均显著高于其他各组(P < 0.05)。Angⅱ输注导致剂量相关百分比变化,RBF增加,RVR降低。然而,ovx -雌二醇和ovx -高血压大鼠的这些反应明显低于ovx -对照组(P < 0.05)。例如,给药剂量为1000 ng/kg/min时,1 ~ 3组RBF变化百分比分别为45.1±10.4%、17.9±2.3%和16.7±4.7%。结论:氯沙坦在某些情况下如高血压或ERT会加重RBF和RVR对Angⅱ的反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Estradiol Supplement or Induced Hypertension May Attenuate the Angiotensin II Type 1 Receptor Antagonist-Promoted Renal Blood Flow Response to Graded Angiotensin II Administration in Ovariectomized Rats.

Estradiol Supplement or Induced Hypertension May Attenuate the Angiotensin II Type 1 Receptor Antagonist-Promoted Renal Blood Flow Response to Graded Angiotensin II Administration in Ovariectomized Rats.

Estradiol Supplement or Induced Hypertension May Attenuate the Angiotensin II Type 1 Receptor Antagonist-Promoted Renal Blood Flow Response to Graded Angiotensin II Administration in Ovariectomized Rats.

Estradiol Supplement or Induced Hypertension May Attenuate the Angiotensin II Type 1 Receptor Antagonist-Promoted Renal Blood Flow Response to Graded Angiotensin II Administration in Ovariectomized Rats.

Backgrounds: Estrogen replacement therapy (ERT) and hypertension may influence females' renin-angiotensin system (RAS) and its components. The angiotensin II (Ang II) type 1 receptor (AT1R) antagonist (losartan) may promote renal blood flow (RBF), and it is widely used in the clinic to control hypertension. The main objective of this study was the effects of estradiol or induced hypertension on RBF response to Ang II in losartan-treated ovariectomized (OVX) rats.

Methods: Two groups of OVX rats were treated with placebo (group 1) and estradiol (group 2) for period of four weeks, and another group of OVX rats was subjected to induce hypertension by two-kidney one clip (2K1C) model (group 3). All the groups were subjected to the surgical procedure under anesthesia, and AT1R was blocked by losartan. RBF and renal vascular resistance (RVR) responses to Ang II administration were determined and compared.

Results: Mean arterial (MAP) and renal perfusion (RPP) pressures in group 3 and uterus weight (UT) in group 2 were significantly more than other groups (P < 0.05). Ang II infusion resulted in dose-related percentage change increase in RBF and decrease in RVR. However, these responses in the OVX-estradiol and OVX-hypertensive rats were significantly lower than in the OVX-control group (P < 0.05). For instance, at the dose of 1000 ng/kg/min of Ang II administration, the percentage change of RBF was 45.1 ± 10.4%, 17.9 ± 2.3%, and 16.7 ± 4.7% in the groups of 1 to 3, respectively.

Conclusion: Losartan prescription in some conditions such as hypertension or ERT could worsen RBF and RVR responses to Ang II.

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来源期刊
CiteScore
6.20
自引率
0.00%
发文量
16
审稿时长
6-12 weeks
期刊介绍: JRAAS is a peer-reviewed, open access journal, serving as a resource for biomedical professionals, primarily with an active interest in the renin-angiotensin-aldosterone system in humans and other mammals. It publishes original research and reviews on the normal and abnormal function of this system and its pharmacology and therapeutics, mostly in a cardiovascular context but including research in all areas where this system is present, including the brain, lungs and gastro-intestinal tract.
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