首页> 外文期刊>Neurochemical research >18 beta-Glycyrrhetinic Acid, a Novel Naturally Derived Agent, Suppresses Prolactin Hyperactivity and Reduces Antipsychotic-Induced Hyperprolactinemia in In Vitro and In Vivo Models
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18 beta-Glycyrrhetinic Acid, a Novel Naturally Derived Agent, Suppresses Prolactin Hyperactivity and Reduces Antipsychotic-Induced Hyperprolactinemia in In Vitro and In Vivo Models

机译:18β-甘草次酸,一种新型的自然衍生药物,在体内和体外模型中抑制催乳激素过度活跃并减少抗精神病药物引起的催乳激素过多

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The purpose of this study was to examine the effects of 18 beta-glycyrrhetinic acid (GA), a novel naturally derived agent, in suppressing prolactin (PRL) hyperactivity and reducing antipsychotic-induced hyperprolactinemia (hyperPRL) and the underlying mechanisms in in vitro and in vivo models. GA treatment for 24 h inhibited PRL synthesis and secretion in MMQ cells and cultured pituitary cells in a dose-dependent fashion; but this effect was not reproduced in GH3 cells that lack the expression of functional dopamine D-2 receptors. GA suppressed elevated PRL level and growth hormone, and normalized several sex hormones in a rat model of hyperPRL, produced by repeated injection of the dopamine blocker metoclopramide. GA also modulated the expression 5-HT1A and 5-HT2A receptors in both in vivo and in vitro models. These results indicate that GA is effective in suppressing PRL hyperactivity caused by the blockade of dopamine D2 receptors. This suppressive effect of GA may be related to its modulation of the serotonergic system. This study provides additional evidence in support of GA as an adjunct for the treatment of hyperPRL.
机译:这项研究的目的是研究一种18β-甘草次酸(GA)(一种新型的天然来源药物)在抑制催乳激素(PRL)过度活跃和减少抗精神病药物引起的高催乳激素血症(hyperPRL)中的作用及其在体外和体内的潜在机制。体内模型。 GA处理24小时以剂量依赖的方式抑制MMQ细胞和垂体细胞中PRL的合成和分泌;但是这种作用在缺乏功能性多巴胺D-2受体表达的GH3细胞中没有再现。在通过反复注射多巴胺阻滞剂甲氧氯普胺产生的hyperPRL大鼠模型中,GA抑制了PRL水平和生长激素的升高,并使几种性激素正常化。 GA还可以在体内和体外模型中调节5-HT1A和5-HT2A受体的表达。这些结果表明,GA有效地抑制了由多巴胺D2受体的阻断引起的PRL过度活跃。 GA的这种抑制作用可能与其对血清素能系统的调节有关。这项研究提供了其他证据支持GA作为hyperPRL的辅助治疗。

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