首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Inhibition by pentobarbitone and urethane of the in vitro response of the adenohypophysis to luteinising hormone-releasing hormone in male rats.
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Inhibition by pentobarbitone and urethane of the in vitro response of the adenohypophysis to luteinising hormone-releasing hormone in male rats.

机译:戊巴比妥和氨基甲酸酯抑制雄性大鼠垂体腺垂体对黄体生成激素释放激素的体外反应。

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摘要

1 The effect of urethane (ethyl carbamate) and sodium pentobarbitone on the luteinising hormone-releasing hormone (LH-RH)-stimulated secretion of luteinising hormone (LH) was investigated with hemipituitaries obtained from male rats and incubated in vitro. 2 Urethane and pentobarbitone were added to the incubation medium to provide final concentrations of 2.2 mg or 4 micrograms/ml and 100 micrograms or 0.1 microgram/ml respectively. The high doses of these anaesthetics blocked the LH-RH stimulated secretion of LH. The low doses significantly reduced the amounts of LH released in response to LH-RH but did not block the response completely. 3 Both concentrations of urethane reduced the basal release of LH. 4 The inhibitory action of the anaesthetics was reversible. 5 The results indicate that the two anaesthetics most commonly used in neuroendocrine experiments have a significant inhibitory action on the release of LH from the adenohypophysis.
机译:1用雄性大鼠的半垂体并进行了体外培养,研究了尿烷(氨基甲酸乙酯)和戊巴比妥钠对促黄体生成素释放激素(LH-RH)刺激的促黄体生成激素(LH)分泌的影响。将2种氨基甲酸酯和戊巴比妥分别添加到温育培养基中,以分别提供2.2毫克或4微克/毫升和100微克或0.1微克/毫升的最终浓度。这些高剂量的麻醉剂阻断了LH-RH刺激的LH分泌。低剂量显着降低了对LH-RH的应答释放的LH量,但并未完全阻断应答。 3两种浓度的氨基甲酸酯都降低了LH的基础释放。 4麻醉药的抑制作用是可逆的。 5结果表明,神经内分泌实验中最常用的两种麻醉剂对LH从腺垂体的释放具有明显的抑制作用。

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