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儿茶酚胺通过与α-和β-肾上腺素能受体相互作用,刺激未成熟金黄仓鼠睾丸释放睾酮。

Catecholamines stimulate testicular testosterone release of the immature golden hamster via interaction with alpha- and beta-adrenergic receptors.

作者信息

Mayerhofer A, Steger R W, Gow G, Bartke A

机构信息

Department of Physiology, School of Medicine, Southern Illinois University, Carbondale.

出版信息

Acta Endocrinol (Copenh). 1992 Dec;127(6):526-30. doi: 10.1530/acta.0.1270526.

Abstract

Several lines of evidence suggest that catecholamines are involved in the regulation of the development of the testis. We have therefore investigated the ability of testicular parenchyma (decapsulated pieces of testes) from 18 to 20-day-old golden hamsters to respond to catecholaminergic stimuli in vitro. Norepinephrine and epinephrine, as well as the beta-receptor agonist isoproterenol and the alpha-adrenoreceptor agonist phenylephrine were able to significantly stimulate testicular testosterone production. Dopamine and serotonin were not effective. The stimulatory action of norepinephrine on testosterone production was dependent on the concentration. In incubations of testes with human chorionic gonadotropin (hCG) and norepinephrine, no synergistic effects on testosterone release were observed. The stimulatory effect of norepinephrine could be partially blocked by incubation with beta-receptor antagonist propranolol, or with alpha-receptor antagonist prazosin, while a combination of propranolol and prazosin completely inhibited the norepinephrine-induced testosterone production. Moreover, isoproterenol and phenylephrine in combination stimulated testosterone more than either drug did alone. Measurements of concentrations of norepinephrine and epinephrine in testicular homogenates revealed higher values for these catecholamines than in the plasma, implying that catecholamine levels in the interstitial spaces of the testis might be in the range of concentrations effectively stimulating testosterone production in vitro. This suggests that in the immature testis of the golden hamster, catecholamines acting through both alpha- and beta-adrenergic receptors may be potent physiological stimulators of testosterone production.

摘要

多项证据表明,儿茶酚胺参与睾丸发育的调节。因此,我们研究了18至20日龄金黄地鼠的睾丸实质(去除被膜的睾丸组织块)在体外对儿茶酚胺能刺激的反应能力。去甲肾上腺素、肾上腺素、β受体激动剂异丙肾上腺素和α肾上腺素能受体激动剂去氧肾上腺素均能显著刺激睾丸睾酮的产生。多巴胺和5-羟色胺无效。去甲肾上腺素对睾酮产生的刺激作用取决于浓度。在睾丸与人绒毛膜促性腺激素(hCG)和去甲肾上腺素共同孵育时,未观察到对睾酮释放的协同作用。去甲肾上腺素的刺激作用可被与β受体拮抗剂普萘洛尔或α受体拮抗剂哌唑嗪共同孵育部分阻断,而普萘洛尔和哌唑嗪联合使用则完全抑制去甲肾上腺素诱导的睾酮产生。此外,异丙肾上腺素和去氧肾上腺素联合使用比单独使用任何一种药物对睾酮的刺激作用更强。对睾丸匀浆中去甲肾上腺素和肾上腺素浓度的测量显示,这些儿茶酚胺在睾丸中的浓度高于血浆中的浓度,这意味着睾丸间质空间中的儿茶酚胺水平可能处于体外有效刺激睾酮产生的浓度范围内。这表明,在金黄地鼠未成熟的睾丸中,通过α和β肾上腺素能受体起作用的儿茶酚胺可能是睾酮产生的有效生理刺激物。

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