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突触前α2肾上腺素能受体介导的去甲肾上腺素释放调节在青年和成年自发性高血压大鼠灌注肠系膜血管中的作用

Presynaptic alpha 2-adrenoceptor mediated regulation of norepinephrine release in perfused mesenteric vasculatures in young and adult spontaneously hypertensive rats.

作者信息

Tsuda K, Kuchii M, Nishio I, Masuyama Y

出版信息

Jpn Circ J. 1987 Jan;51(1):25-32. doi: 10.1253/jcj.51.25.

Abstract

The present study was designed to evaluate the role of the presynaptic alpha 2-adrenoceptor in the pathogenesis of hypertension. Norepinephrine overflow during sympathetic nerve stimulation and its changes by presynaptic alpha 2-adrenoceptor inhibition were examined in the perfused mesenteric vasculatures of young and adult spontaneously hypertensive rats (SHR) compared with age-matched Wistar Kyoto rats (WKY). Electrical sympathetic nerve stimulation caused significantly greater overflow of endogenous norepinephrine from the adrenergic nerve terminals in young SHR than in age-matched WKY. Yohimbine, an alpha 2-adrenoceptor blocking agent, facilitated norepinephrine overflow from the adrenergic nerve terminals. The effects of yohimbine on norepinephrine overflow and pressor responses to electrical nerve stimulation were less in young SHR than in age-matched WKY. Norepinephrine overflow in adult SHR was similar to that in adult WKY, and differences in the effect of yohimbine on norepinephrine overflow between SHR and WKY were not marked at this chronic stage. These results suggest that enhanced norepinephrine overflow in the mesenteric vasculatures can be observed only in young SHR; this may be due in part to an impaired negative feed-back mechanism on the nerve terminals by presynaptic alpha 2-adrenoceptors.

摘要

本研究旨在评估突触前α₂肾上腺素能受体在高血压发病机制中的作用。在年轻和成年自发性高血压大鼠(SHR)的灌注肠系膜血管系统中,检测交感神经刺激期间去甲肾上腺素的溢出情况以及突触前α₂肾上腺素能受体抑制对其的影响,并与年龄匹配的Wistar Kyoto大鼠(WKY)进行比较。电刺激交感神经时,年轻SHR肾上腺素能神经末梢内源性去甲肾上腺素的溢出量显著高于年龄匹配的WKY。α₂肾上腺素能受体阻断剂育亨宾可促进肾上腺素能神经末梢释放去甲肾上腺素。育亨宾对年轻SHR去甲肾上腺素溢出和电刺激神经引起的升压反应的影响小于年龄匹配的WKY。成年SHR的去甲肾上腺素溢出与成年WKY相似,在这个慢性阶段,SHR和WKY之间育亨宾对去甲肾上腺素溢出影响的差异并不明显。这些结果表明,仅在年轻SHR的肠系膜血管系统中可观察到去甲肾上腺素溢出增强;这可能部分归因于突触前α₂肾上腺素能受体对神经末梢的负反馈机制受损。

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