首页> 美国卫生研究院文献>American Journal of Physiology - Regulatory Integrative and Comparative Physiology >Estrogen replacement restores flow-induced vasodilation in coronary arterioles of aged and ovariectomized rats
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Estrogen replacement restores flow-induced vasodilation in coronary arterioles of aged and ovariectomized rats

机译:雌激素替代可恢复衰老和去卵巢大鼠冠状动脉的血流诱导的血管舒张

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摘要

The risk for cardiovascular disease (CVD) increases with advancing age; however, the age at which CVD risk increases significantly is delayed by more than a decade in women compared with men. This cardioprotection, which women experience until menopause, is presumably due to the presence of ovarian hormones, in particular, estrogen. The purpose of this study was to determine how age and ovarian hormones affect flow-induced vasodilation in the coronary resistance vasculature. Coronary arterioles were isolated from young (6 mo), middle-aged (14 mo), and old (24 mo) intact, ovariectomized (OVX), and ovariectomized + estrogen replaced (OVE) female Fischer-344 rats to assess flow-induced vasodilation. Advancing age impaired flow-induced dilation of coronary arterioles (young: 50 ± 4 vs. old: 34 ± 6; % relaxation). Ovariectomy reduced flow-induced dilation in arterioles from young females, and estrogen replacement restored vasodilation to flow. In aged females, flow-induced vasodilation of arterioles was unaltered by OVX; however, estrogen replacement improved flow-induced dilation by ∼160%. The contribution of nitric oxide (NO) to flow-induced dilation, assessed by nitric oxide synthase (NOS) inhibition with NG-nitro-l-arginine methyl ester (l-NAME), declined with age. l-NAME did not alter flow-induced vasodilation in arterioles from OVX rats, regardless of age. In contrast, l-NAME reduced flow-induced vasodilation of arterioles from estrogen-replaced rats at all ages. These findings indicate that the age-induced decline of flow-induced, NO-mediated dilation in coronary arterioles of female rats is related, in part, to a loss of ovarian estrogen, and estrogen supplementation can improve flow-induced dilation, even at an advanced age.
机译:随着年龄的增长,心血管疾病(CVD)的风险增加;然而,与男性相比,女性心血管疾病风险显着增加的年龄被推迟了十多年。妇女直到更年期才经历的这种心脏保护作用可能是由于存在卵巢激素,尤其是雌激素。这项研究的目的是确定年龄和卵巢激素如何影响冠脉阻力血管系统中血流诱导的血管舒张。从完整的年轻(6 mo),中年(14 mo)和老年(24 mo),去卵巢(OVX)和去卵巢+雌激素替代(OVE)雌性Fischer-344大鼠中分离冠状小动脉,以评估血流诱导血管舒张。年龄增加会损害血流引起的冠状小动脉扩张(年轻:50±4 vs.老:34±6;%松弛)。卵巢切除术减少了年轻女性的小动脉血流诱发的扩张,雌激素替代使血管扩张恢复了血流。在老年女性中,OVX不会改变血流引起的小动脉血管舒张作用。然而,雌激素替代可将血流诱发的扩张改善约160%。 N G -硝基-1-精氨酸甲酯(l-NAME)对一氧化氮合酶(NOS)的抑制作用评估一氧化氮(NO)对流量诱导的扩张的贡献随着年龄的增长而下降。无论年龄大小,l-NAME都不会改变OVX大鼠小动脉的血流诱导性血管舒张作用。相反,l-NAME降低了所有年龄段的雌激素替代大鼠的血流诱导的小动脉血管舒张。这些发现表明,年龄引起的雌性大鼠冠状小动脉血流诱导的,NO介导的扩张的下降部分与卵巢雌激素的丢失有关,补充雌激素可以改善血流诱导的扩张,即使在高龄。

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