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血管加压素对侏儒山羊血浆游离脂肪酸和甘油三酯水平影响的机制。

Mechanisms of the effects of vasopressin on plasma levels of free fatty acids and triglycerides in pygmy goats.

作者信息

Rossi R, Scharrer E

机构信息

Institut für Veterinär-Physiologie, Universität Zürich, Switzerland.

出版信息

Comp Biochem Physiol Comp Physiol. 1993 Feb;104(2):287-90. doi: 10.1016/0300-9629(93)90319-y.

Abstract
  1. Intraperitoneal injection of vasopressin (VP, 0.4 or 0.75 microgram/kg body wt) produced a decrease in plasma free fatty acids (FFA) and an increase in plasma triglyceride (TG) levels in pygmy goats. 2. These effects were not attenuated by prior or co-injection of a vasopressin antagonist with a selective affinity to V1-receptors. 3. A vasopressin antagonist with predominant affinity to V2-receptors prevented vasopressin's effect on plasma lipid levels whereas a V2-receptor agonist did not significantly influence plasma lipids. 4. The effect of vasopressin on plasma lipids in pygmy goats therefore seems to be mediated by receptors being neither identical with V1- or V2-receptors.
摘要
  1. 向侏儒山羊腹腔注射加压素(VP,0.4或0.75微克/千克体重)会导致血浆游离脂肪酸(FFA)减少,血浆甘油三酯(TG)水平升高。2. 预先注射或同时注射对V1受体具有选择性亲和力的加压素拮抗剂并不能减弱这些作用。3. 对V2受体具有主要亲和力的加压素拮抗剂可阻止加压素对血浆脂质水平的影响,而V2受体激动剂对血浆脂质没有显著影响。4. 因此,加压素对侏儒山羊血浆脂质的作用似乎是由既不同于V1受体也不同于V2受体的受体介导的。

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