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[通过改变个体发育早期的儿茶酚胺代谢来纠正遗传性高血压大鼠的动脉血压]

[Correction of arterial pressure in rats with hereditary hypertension by altering catecholamine metabolism in early ontogeny].

作者信息

Naumenko E V, Maslova L N, Markel' A L, Gordienko N I

出版信息

Biull Eksp Biol Med. 1987 Oct;104(10):464-6.

PMID:3676471
Abstract

In a newly developed rat strain with inherited stress-sensitive arterial hypertension (ISSAH) an attempt was made to reduce arterial blood pressure by L-DOPA injections during a short time period of the early ontogenesis. It was shown that L-DOPA injections to rats on days 7-9 or 14-16 of life had no effect. The same procedure performed on 21-23 or 21-25-day-old rats was followed by a decrease in the basal and stress-induced arterial blood pressure levels, measured in adulthood. Injections of dopamine-beta-hydroxylase inhibitor (FLA-59) with parallel L-DOPA administration completely blocked the blood pressure decreasing effect. It can be suggested that injections of L-DOPA in the 4th week of post-natal life reduce the blood pressure level in ISSAH rats by enhancing the rate of brain noradrenaline biosynthesis.

摘要

在一种新培育的具有遗传性应激敏感性动脉高血压(ISSAH)的大鼠品系中,尝试在个体发育早期的短时间内通过注射左旋多巴来降低动脉血压。结果表明,在出生后第7 - 9天或14 - 16天给大鼠注射左旋多巴没有效果。而在21 - 23日龄或21 - 25日龄大鼠上进行相同操作后,成年期测量的基础血压和应激诱导的动脉血压水平均有所下降。同时注射多巴胺 - β - 羟化酶抑制剂(FLA - 59)与左旋多巴完全阻断了血压降低的效果。可以推测,出生后第4周注射左旋多巴可通过提高脑去甲肾上腺素的生物合成速率来降低ISSAH大鼠的血压水平。

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