The angiotensin II type 2 receptor attenuates aging-associated arterial stiffness in female mice.

IF 4.1 2区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Casey G Turner, Rachel Kenney, Jennifer Vorn, Seung Kyum Kim, Gregory Martin, Lakshmi Pulakat, Iris Z Jaffe, Jennifer J DuPont
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引用次数: 0

Abstract

Arterial stiffness is associated with overall and cardiovascular-specific mortality, and this association is exacerbated in women over 55-years-old. Recent literature supports that stimulation of the angiotensin II type 2 receptor (AT2R) can protect from arterial stiffening, and that AT2R has a greater role in female cardiovascular physiology relative to males. The current study aimed to investigate the role of the AT2R in sex differences in aging-associated arterial stiffness. In female mice, the aging-related increase in arterial stiffness is temporally associated with a loss of aortic AT2R mRNA expression, but this is not observed in males. Chronic AT2R inhibition in vivo increases arterial stiffening in young female and male mice, as well as middle-aged female mice. The inhibition of AT2R is associated with an increase in aortic integrinα5 mRNA expression in young males and an increase in collagen1α1 mRNA expression in middle-aged females. Overall, these findings identify a sex-specific mechanism of aging-associated arterial stiffening in mice involving AT2R attenuation and collagen upregulation in females.

血管紧张素II型2受体减轻雌性小鼠衰老相关的动脉僵硬。
动脉僵硬与总体死亡率和心血管特异性死亡率相关,这种关联在55岁以上的女性中更为明显。最近的文献支持刺激血管紧张素II型2受体(AT2R)可以防止动脉硬化,并且与男性相比,AT2R在女性心血管生理中具有更大的作用。目前的研究旨在探讨AT2R在与年龄相关的动脉硬度的性别差异中的作用。在雌性小鼠中,与衰老相关的动脉硬度增加与主动脉AT2R mRNA表达的缺失暂时相关,但在雄性小鼠中没有观察到这一点。体内慢性AT2R抑制增加了年轻雌性和雄性小鼠以及中年雌性小鼠的动脉硬化。AT2R的抑制与年轻男性主动脉整合素α5 mRNA表达增加和中年女性胶原1α1 mRNA表达增加有关。总的来说,这些发现确定了一种性别特异性的衰老相关动脉硬化机制,涉及雌性小鼠的AT2R衰减和胶原蛋白上调。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.60
自引率
10.40%
发文量
202
审稿时长
2-4 weeks
期刊介绍: The American Journal of Physiology-Heart and Circulatory Physiology publishes original investigations, reviews and perspectives on the physiology of the heart, vasculature, and lymphatics. These articles include experimental and theoretical studies of cardiovascular function at all levels of organization ranging from the intact and integrative animal and organ function to the cellular, subcellular, and molecular levels. The journal embraces new descriptions of these functions and their control systems, as well as their basis in biochemistry, biophysics, genetics, and cell biology. Preference is given to research that provides significant new mechanistic physiological insights that determine the performance of the normal and abnormal heart and circulation.
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