Lawson D M, Gala R R
J Endocrinol. 1975 Aug;66(2):151-7. doi: 10.1677/joe.0.0660151.
Plasma levels of prolactin were determined, by radioimmunoassay, in ovariectomized, oestrogen-treated rats after administration of ether, sodium pentobarbitone, urethane, chloral hydrate or ketamine. These anaesthetics, when administered alone, induced sustained increases in the plasma level of prolactin (continuous ether inhalation), no change in prolactin secretion (urethane), or depressions in the level of prolactin (sodium pentobarbitone, chloral hydrate and ketamine). These same anaesthetics when given before perphenazine failed to alter the stimulatory effect of this phenothiazide on prolactin secretion. Sodium pentobarbitone did not alter the normal increase in prolactin concentration after intra-arterial administration of synthetic thyrotrophin releasing hormone (TRH). These results indicated that anaesthetics do not affect the response of either the central nervous system or the anterior pituitary to perphenazine or TRH although they affect prolactin secretion when administered alone. The site of action of anaesthetics must, therefore, be different from that of perphenazine or perphenazine must be capable of overcoming their influence by direct action on the pituitary.
采用放射免疫分析法,测定了经雌激素处理的去卵巢大鼠在给予乙醚、戊巴比妥钠、乌拉坦、水合氯醛或氯胺酮后血浆催乳素水平。这些麻醉剂单独使用时,可导致催乳素血浆水平持续升高(持续吸入乙醚)、催乳素分泌无变化(乌拉坦)或催乳素水平降低(戊巴比妥钠、水合氯醛和氯胺酮)。在给予奋乃静之前给予这些相同的麻醉剂,未能改变这种吩噻嗪对催乳素分泌的刺激作用。戊巴比妥钠未改变动脉内注射合成促甲状腺激素释放激素(TRH)后催乳素浓度的正常升高。这些结果表明,麻醉剂虽然单独使用时会影响催乳素分泌,但并不影响中枢神经系统或垂体前叶对奋乃静或TRH的反应。因此,麻醉剂的作用部位一定与奋乃静不同,或者奋乃静一定能够通过直接作用于垂体来克服它们的影响。