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大鼠使用抗精神病药物和多潘立酮诱导高泌乳素血症后垂体对促性腺激素释放激素的敏感性

Pituitary sensitivity to gonadotrophin releasing hormone after hyperprolactinaemia induced with neuroleptics and domperidone in the rat.

作者信息

Carter D A, Whitehead S A

出版信息

J Endocrinol. 1981 Dec;91(3):439-46. doi: 10.1677/joe.0.0910439.

Abstract

The effect of hyperprolactinaemia induced by dopamine-antagonist drugs on pituitary responsiveness to gonadotrophin releasing hormone (Gn-RH) and on plasma LH levels has been investigated in intact and ovariectomized rats. The animals were pretreated with haloperidol, pimozide or domperidone and the sensitivity of isolated pituitary glands to pulses of Gn-RH were tested using a perifusion system. Trunk blood, collected at the time of killing, was assayed for plasma LH and prolactin. In addition, a direct effect of the drugs on pituitary responsiveness to Gn-RH was investigated by perfusing pituitary glands taken from untreated, pro-oestrous rats in medium containing the dopamine antagonists. The pituitary responsiveness was significantly impaired in intact rats after treatment with each of the drugs whereas no effect was observed in pretreated ovariectomized rats. None of the drug treatments altered levels of circulating LH. High concentrations of the drugs present in the perifusion medium also inhibited pituitary responsiveness although it is not known whether the concentrations of the drugs present in the pretreated animals would exert a similar effect. The results suggest that short-term hyperprolactinaemia impairs pituitary responsiveness through a modulation of ovarian steroid secretion and that Gn-RH release is not altered. Treatment with domperidone exhibited similar effects on the parameters measured here to those caused by the two neuroleptics, indicating that this novel anti-dopaminergic drug is acting in a similar manner.

摘要

在完整大鼠和去卵巢大鼠中,研究了多巴胺拮抗剂药物诱导的高催乳素血症对垂体促性腺激素释放激素(Gn-RH)反应性及血浆促黄体生成素(LH)水平的影响。给动物预先使用氟哌啶醇、匹莫齐特或多潘立酮,然后使用灌流系统测试分离的垂体对Gn-RH脉冲的敏感性。处死动物时采集躯干血,检测血浆LH和催乳素。此外,通过在含有多巴胺拮抗剂的培养基中灌流取自未处理的动情前期大鼠的垂体,研究药物对垂体Gn-RH反应性的直接影响。用每种药物处理后,完整大鼠的垂体反应性显著受损,而预先处理的去卵巢大鼠未观察到影响。药物处理均未改变循环LH水平。灌流培养基中高浓度的药物也抑制垂体反应性,尽管尚不清楚预先处理动物体内的药物浓度是否会产生类似作用。结果表明,短期高催乳素血症通过调节卵巢类固醇分泌损害垂体反应性,且Gn-RH释放未改变。多潘立酮处理对这里测量的参数产生的影响与两种抗精神病药物引起的影响相似,表明这种新型抗多巴胺能药物的作用方式类似。

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