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内皮素在下丘脑内发挥作用诱导心房利钠肽释放和利钠作用的潜在机制。

Possible role of endothelin acting within the hypothalamus to induce the release of atrial natriuretic peptide and natriuresis.

作者信息

Antunes-Rodrigues J, Ramalho M J, Reis L C, Picanco-Diniz D W, Favaretto A L, Gutkowska J, McCann S M

机构信息

Department of Physiology, School of Medicine, University of Saõ Paulo, Ribeiraõ Preto, Brazil.

出版信息

Neuroendocrinology. 1993 Dec;58(6):701-8. doi: 10.1159/000126612.

Abstract

Since endothelin has been localized in neurons in areas involved in water and electrolyte metabolism, areas which also contain atrial natriuretic peptide (ANP) neurons, we determined whether endothelin would release ANP and induce natriuresis. Endothelin-3 (ET-3) in doses ranging from 38 to 760 pmol was microinjected into the third ventricle (3V) of conscious, water-loaded male rats, and the effect on natriuresis and plasma ANP was determined. ET-3 evoked a dose-related natriuresis beginning within 20 min of injection. Even the lowest dose tested (38 pmol) was effective. At a dose of 95 pmol, it produced a rapid increase of plasma ANP within 5 min peaking at 20 min. A slight kaliuresis and antidiuresis was observed at the 2 highest doses of 380 and 760 pmol. The urinary changes following 3V injection of ET-3 were similar to those evoked by ANP, except for the antidiuresis with increased sodium concentration which followed injection of the 2 higher doses. These results suggest that these 2 higher doses also released vasopressin. Alternatively, activation of the sympathetic nervous system by these higher doses may have decreased glomerular filtration rate and been in part responsible for the antidiuresis. The results with 3V injection of ET-3 contrasted sharply with those obtained following intravenous injection of the 95-pmol dose injected intraventricularly. This intravenous dose of ANP induced a transient decrease in sodium and potassium excretion and urine volume, maximal at 20 min, and had no effect on plasma ANP concentrations at 5 or 20 min after injection.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

由于内皮素已定位在参与水和电解质代谢的脑区神经元中,这些脑区也含有心房利钠肽(ANP)神经元,因此我们确定内皮素是否会释放ANP并诱导利钠作用。将剂量范围为38至760皮摩尔的内皮素-3(ET-3)微量注射到清醒、饮水负荷的雄性大鼠的第三脑室(3V)中,并测定其对利钠作用和血浆ANP的影响。ET-3注射后20分钟内即引起剂量相关的利钠作用。即使是测试的最低剂量(38皮摩尔)也有效。在95皮摩尔的剂量下,它在5分钟内使血浆ANP迅速升高,在20分钟时达到峰值。在380和760皮摩尔这两个最高剂量下观察到轻微的尿钾增多和抗利尿作用。3V注射ET-3后的尿液变化与ANP引起的变化相似,但在注射较高的两个剂量后出现了钠浓度升高的抗利尿作用。这些结果表明,这两个较高剂量也释放了血管加压素。或者,这些较高剂量激活交感神经系统可能降低了肾小球滤过率,部分导致了抗利尿作用。3V注射ET-3的结果与脑室内注射95皮摩尔剂量后静脉注射的结果形成鲜明对比。静脉注射该剂量的ANP可导致钠、钾排泄和尿量短暂减少,在20分钟时达到最大值,且在注射后5或20分钟对血浆ANP浓度无影响。(摘要截断于250字)

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