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血清素能受体在雄性大鼠促性腺激素分泌中的作用。

Role of serotoninergic receptors in gonadotropin secretion in male rats.

作者信息

Pinilla L, Tena-Sempere M, Aguilar E

机构信息

Department of Physiology, Faculty of Medicine, Córdoba University, Spain.

出版信息

J Endocrinol Invest. 1997 Jul-Aug;20(7):410-6. doi: 10.1007/BF03347993.

Abstract

Experimental data concerning the role of serotonin (5-HT) in the control of gonadotropins secretion remain controversial: different receptors subtypes should mediate the serotoninergic action. In the present work we analyzed in prepubertal and adult male rats the FSH and LH responses after administration of the following drugs: 5-hydroxy-L-tryptophan (5-HTP), precursor of 5-HT synthesis, the 5-HT1 receptor agonist 8-hydroxy-2-(di-n-propylamino) tetralin (8-OH-DPAT), the 5-HT2 receptor agonists alpha-methylserotonin maleate (alpha-CH3-HT) and (+/-)-DOI hydrochloride (DOI), the 5-HT3 agonists, quipazine-N-methyldimaleate (QUIP), 2 methyl-serotonin maleate (2-CH3-HT), trimethylserotonin iodide (5-HTQ) and 1-phenylbiguanide (PHE). We found that: a) FSH secretion in adult males was stimulated by 5-HTP, inhibited by 5-HT2 agonists and unaffected by 5-HT3 agonists; b) LH secretion in adult males was stimulated by 5-HTP and alpha-CH3-HT, while DOI and 5-HT3 agonists were ineffective; c) in prepubertal males, 5-HT2 and 5-HT3 agonists inhibited LH release. All these results taken together suggest that: (1) 5-HT2 and 5-HT3 receptors are involved in the control of gonadotropin secretion; (2) FSH and LH secretion are differently modulated by agonists of 5-HT2 and 5-HT3 receptors; (3) the 5-HT2 agonists alpha-CH3-HT and DOI elicit different responses; and (4) the responses obtained vary with animal age, since the inhibitory effect of 5-HT2 and 5-HT3 agonists on LH secretion was observed only in prepubertal males.

摘要

关于血清素(5-羟色胺,5-HT)在促性腺激素分泌调控中作用的实验数据仍存在争议:不同的受体亚型可能介导血清素能作用。在本研究中,我们分析了青春期前和成年雄性大鼠在给予以下药物后的促卵泡生成素(FSH)和促黄体生成素(LH)反应:5-羟色胺合成前体5-羟-L-色氨酸(5-HTP)、5-HT1受体激动剂8-羟基-2-(二正丙基氨基)四氢萘(8-OH-DPAT)、5-HT2受体激动剂马来酸α-甲基血清素(α-CH3-HT)和盐酸(+/-)-DOI(DOI)、5-HT3激动剂马来酸喹哌嗪-N-甲基二酯(QUIP)、马来酸2-甲基血清素(2-CH3-HT)、碘化三甲基血清素(5-HTQ)和1-苯基双胍(PHE)。我们发现:a)成年雄性大鼠的FSH分泌受到5-HTP刺激,受到5-HT2激动剂抑制,不受5-HT3激动剂影响;b)成年雄性大鼠的LH分泌受到5-HTP和α-CH3-HT刺激,而DOI和5-HT3激动剂无效;c)在青春期前雄性大鼠中,5-HT2和5-HT3激动剂抑制LH释放。综合所有这些结果表明:(1)5-HT2和5-HT3受体参与促性腺激素分泌的调控;(2)FSH和LH分泌受到5-HT2和5-HT3受体激动剂的不同调节;(3)5-HT2激动剂α-CH3-HT和DOI引发不同反应;(4)所获得的反应因动物年龄而异,因为仅在青春期前雄性大鼠中观察到5-HT2和5-HT3激动剂对LH分泌的抑制作用。

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