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首页> 外文期刊>American Journal of Physiology >Reduced release of nitric oxide to shear stress in mesenteric arteries of aged rats.
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Reduced release of nitric oxide to shear stress in mesenteric arteries of aged rats.

机译:减少老年大鼠肠系膜动脉中一氧化氮释放至切应力的作用。

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We hypothesized that aging is characterized by a reduced release of nitric oxide (NO) in response to shear stress in resistance vessels. Mesenteric arterioles and arteries of young (6 mo) and aged (24 mo) male Fischer 344 rats were isolated and cannulated. Shear stress (15 dyn/cm(2))-induced dilation was significantly reduced and shear stress (1, 5, 10, and 15 dyn/cm(2))-induced increases in perfusate nitrite were significantly smaller at all shear stress levels in vessels of aged rats. Inhibition of NO synthesis abolished shear stress-induced release of nitrite. Furthermore, shear stress (15 dyn/cm(2))-induced release of nitrate was significantly higher and total nitrite (nitrite plus nitrate) was significantly lower in vessels of aged rats. Tiron or SOD significantly increased nitrite released from vessels of aged rats, but this was still significantly less than that in young rats. Superoxide production was increased and the activity of SOD was decreased in vessels of aged rats. There were no differences in endothelial NO synthase (eNOS) protein and basal activity or in Cu/Zn-SOD and Mn-SOD proteins in vessels of the two groups, but extracellular SOD was significantly reduced in vessels of aged rats. Maximal release of NO induced by shear stress plus ACh (10(-5) M) was comparable in the two groups, but phospho-eNOS in response to shear stress (15 dyn/cm(2)) was significantly reduced in vessels of aged rats. These data suggest that an increased production of superoxide, a reduced activity of SOD, and an impaired shear stress-induced activation of eNOS are the causes of the decreased shear stress-induced release of NO in vessels of aged rats.
机译:我们假设老化的特征是响应阻力容器中的剪切应力而减少的一氧化氮(NO)释放。分离并插管幼年(6 mo)和老年(24 mo)Fischer 344大鼠的肠系膜小动脉和动脉。在所有剪切应力水平下,剪切应力(15 dyn / cm(2))引起的膨胀都显着降低,剪切应力(1、5、10、15 dyn / cm(2))引起的灌注液亚硝酸盐增加显着减小在老年大鼠的血管中。 NO合成的抑制消除了剪切应力引起的亚硝酸盐释放。此外,在老年大鼠的血管中,剪应力(15 dyn / cm(2))诱导的硝酸盐释放明显更高,总亚硝酸盐(亚硝酸盐加硝酸盐)明显更低。 Tiron或SOD显着增加了老年大鼠血管中释放的亚硝酸盐,但仍显着低于年轻大鼠。老龄大鼠血管中超氧化物的产生增加,SOD活性降低。两组血管内皮NO合酶(eNOS)蛋白和基础活性或Cu / Zn-SOD和Mn-SOD蛋白无差异,但老年大鼠血管中细胞外SOD明显降低。剪切应力加ACh(10(-5)M)诱导的NO的最大释放在两组中相当,但是在衰老的血管中,磷-eNOS响应剪切应力(15 dyn / cm(2))明显降低大鼠。这些数据表明,超氧化物的产生增加,SOD活性降低以及剪切应力诱导的eNOS活化受损是衰老大鼠血管中剪切应力诱导的NO释放减少的原因。

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