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[血管周围神经在胰岛素抵抗诱导的高血压中的作用]

[Function of Perivascular Nerves in Insulin Resistance-induced Hypertension].

作者信息

Takatori Shingo

机构信息

Department of Clinical Pharmaceutical Science, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University.

出版信息

Yakugaku Zasshi. 2017;137(11):1367-1371. doi: 10.1248/yakushi.17-00149.

Abstract

Many patients with type 2 diabetes mellitus develop hypertension, although the actual mechanism remains unknown. To clarify possible mechanisms of hypertension development in diabetes, this study investigated the acute or chronic influence of hyperinsulinemia and/or hyperglycemia on the function of perivascular nerves, which play a critical role in vascular tone regulation. Acute hyperinsulinemia in euglycemic pithed rats, which had no autonomic flow, significantly augmented adrenergic nerve-mediated pressor responses and inhibited calcitonin gene-related peptide (CGRP)-containing (CGRPergic) nerve-mediated depressor responses. To increase blood glucose levels without changing serum insulin levels, pithed rats were treated with octreotide. In this model, acute hyperglycemia produced only marked enhancement of adrenergic nerve-mediated vasoconstriction. Chronic hyperinsulinemia in insulin resistance model rats caused significant increases in the function and distribution of perivascular sympathetic nerves and decreases in those of perivascular CGRPergic nerves, resulting in the development of hypertension (insulin resistance-induced hypertension). Treatment with pioglitazone or functional foods with an insulin resistance-improving effect prevented the development of insulin resistance-induced hypertension. The present studies suggest that acute and chronic hyperinsulinemia reduces vasodilator function of perivascular CGRPergic nerves and enhances the vasoconstrictor function of perivascular adrenergic nerves, leading to the development of hypertension. The results also indicate that hyperinsulinemia and hyperglycemia may have a crucial role in the alteration of neuronal vascular tone regulation.

摘要

许多2型糖尿病患者会并发高血压,但其具体机制尚不清楚。为了阐明糖尿病患者高血压发生的可能机制,本研究调查了高胰岛素血症和/或高血糖对血管周围神经功能的急性或慢性影响,这些神经在血管张力调节中起关键作用。在无自主血流的去大脑大鼠中,急性高胰岛素血症显著增强了肾上腺素能神经介导的升压反应,并抑制了降钙素基因相关肽(CGRP)能神经介导的降压反应。为了在不改变血清胰岛素水平的情况下升高血糖水平,给去大脑大鼠注射了奥曲肽。在该模型中,急性高血糖仅显著增强了肾上腺素能神经介导的血管收缩。胰岛素抵抗模型大鼠的慢性高胰岛素血症导致血管周围交感神经的功能和分布显著增加,而血管周围CGRP能神经的功能和分布则减少,从而导致高血压(胰岛素抵抗性高血压)的发生。使用吡格列酮或具有改善胰岛素抵抗作用的功能性食品进行治疗可预防胰岛素抵抗性高血压的发生。本研究表明,急性和慢性高胰岛素血症均会降低血管周围CGRP能神经的舒张血管功能,并增强血管周围肾上腺素能神经的收缩血管功能,从而导致高血压的发生。研究结果还表明,高胰岛素血症和高血糖可能在神经元血管张力调节的改变中起关键作用。

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