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多巴胺在自发性高血压发展中的作用。

Role of dopamine in the development of spontaneous hypertension.

作者信息

van den Buuse M, Versteeg D H, de Jong W

出版信息

Hypertension. 1984 Nov-Dec;6(6 Pt 1):899-905. doi: 10.1161/01.hyp.6.6.899.

Abstract

To investigate the role of brain catecholamines in the development of spontaneous hypertension, rats were treated with different doses of the neurotoxins 6-hydroxydopamine (6-OHDA) or DSP-4 (N-[2-chloroethyl]-N-ethyl-2-bromobenzylamine hydrochloride). Intracerebroventricular (i.c.v.) 6-OHDA attenuated the development of hypertension in spontaneously hypertensive rats (SHR) and also lowered the systolic blood pressure (BP) in Wistar-Kyoto (WKY) and stroke-prone spontaneously hypertensive rats (SHRSP). Norepinephrine was markedly and dose-dependently depleted in brain areas of all three substrains. Dopamine was affected also, although to a lesser extent. Pretreatment with the norepinephrine-uptake inhibitor desmethylimipramine (DMI) did not influence the effect of 6-OHDA on the development of hypertension in SHR. DMI largely antagonized the 6-OHDA-induced depletion of brain norepinephrine, while dopamine depletion was not affected. Specific depletion of brain norepinephrine by treatment with DSP-4 did not alter the rise in BP in SHR. These results suggest that the effect of 6-OHDA on the development of hypertension in SHR may not be mediated through destruction of brain norepinephrine neurons, but that interruption of brain dopaminergic mechanisms is a possibility in this respect.

摘要

为了研究脑内儿茶酚胺在自发性高血压发生发展中的作用,用不同剂量的神经毒素6-羟基多巴胺(6-OHDA)或DSP-4(N-[2-氯乙基]-N-乙基-2-溴苄胺盐酸盐)处理大鼠。脑室内注射6-OHDA可减轻自发性高血压大鼠(SHR)的高血压发展,并降低Wistar-Kyoto(WKY)大鼠和易卒中型自发性高血压大鼠(SHRSP)的收缩压。所有三个亚系脑区的去甲肾上腺素均明显且呈剂量依赖性地减少。多巴胺也受到影响,尽管程度较轻。用去甲肾上腺素摄取抑制剂去甲丙咪嗪(DMI)预处理并不影响6-OHDA对SHR高血压发展的作用。DMI在很大程度上拮抗了6-OHDA诱导的脑内去甲肾上腺素耗竭,而多巴胺耗竭不受影响。用DSP-4特异性耗竭脑内去甲肾上腺素并未改变SHR血压的升高。这些结果表明,6-OHDA对SHR高血压发展的作用可能不是通过破坏脑内去甲肾上腺素能神经元介导的,但在这方面脑内多巴胺能机制的中断是有可能的。

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