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纳洛酮可抑制氨基甲酸乙酯麻醉的雄性大鼠体内精氨酸加压催产素(AVT)诱导的催乳素释放。

Naloxone inhibits arginine vasotocin- (AVT) induced prolactin release in urethane-anesthetized male rats in vivo.

作者信息

Blask D E, Vaughan M K

出版信息

Neurosci Lett. 1980 Jun;18(2):181-4. doi: 10.1016/0304-3940(80)90323-7.

Abstract

Arginine vasotocin (AVT) (1 microgram) elicited a two-fold increase in serum prolactin (Prl) levels 10 min following its i.v. injection into urethane-anesthetized adult male rats. At 20 min after AVT administration serum Prl concentrations had essentially returned to preinjection levels. Prior treatment of the animals with 0.2 mg/kg body weight of naloxone (Nal), an opiate antagonist, completely blocked the Prl response to a single injection of AVT. Nal itself did not alter the titers of Prl at any time point. The results suggest that the in vivo Prl-releasing effect of AVT is mediated via an interaction with opiate receptors.

摘要

将精氨酸血管加压素(AVT)(1微克)静脉注射到氨基甲酸乙酯麻醉的成年雄性大鼠体内10分钟后,血清催乳素(Prl)水平增加了两倍。在AVT给药后20分钟,血清Prl浓度基本恢复到注射前水平。用0.2毫克/千克体重的阿片拮抗剂纳洛酮(Nal)对动物进行预处理,可完全阻断单次注射AVT引起的Prl反应。Nal本身在任何时间点都不会改变Prl的滴度。结果表明,AVT在体内释放Prl的作用是通过与阿片受体相互作用介导的。

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