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一种强效血管升压素拮抗剂对精氨酸加压素诱导的运动障碍的预防作用。

Prevention of arginine-vasopressin-induced motor disturbances by a potent vasopressor antagonist.

作者信息

Burnard D M, Veale W L, Pittman Q J

出版信息

Brain Res. 1986 Jan 1;362(1):40-6. doi: 10.1016/0006-8993(86)91396-x.

Abstract

The antivasopressor analog d(CH2)5Tyr(Me) arginine-vasopressin completely blocked the convulsive-like behavior and other severe motor disturbances which are normally observed following a second central arginine-vasopressin injection. This vasopressor antagonist appears to be selective for arginine-vasopressin-induced motor disturbances, in that the convulsive and motor effects of pentylenetetrazol and somatostatin were not altered significantly by pretreatment with the central antagonist. Results suggest that arginine-vasopressin-induced motor disturbances are mediated via central receptors. The classic antidiuretic (V2) type of arginine-vasopressin receptor does not appear to be involved, since the agonist 1-desamino-8-D-arginine-vasopressin did not elicit convulsive-like behavior or other severe motor disturbances 2 days following a first ('priming') injection of arginine-vasopressin.

摘要

抗血管升压素类似物d(CH2)5Tyr(Me)精氨酸血管加压素完全阻断了惊厥样行为和其他严重的运动障碍,这些通常在第二次中枢注射精氨酸血管加压素后观察到。这种血管升压素拮抗剂似乎对精氨酸血管加压素诱导的运动障碍具有选择性,因为用中枢拮抗剂预处理后,戊四氮和生长抑素的惊厥和运动效应没有显著改变。结果表明,精氨酸血管加压素诱导的运动障碍是通过中枢受体介导的。经典的抗利尿(V2)型精氨酸血管加压素受体似乎不参与其中,因为激动剂1-去氨基-8-D-精氨酸血管加压素在首次(“预充”)注射精氨酸血管加压素2天后没有引发惊厥样行为或其他严重的运动障碍。

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