[多巴胺能系统在大鼠卵巢中的作用]。

S Isobe
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引用次数: 3

摘要

虽然对多巴胺能系统的研究很多,但对卵巢中的多巴胺能系统知之甚少。本研究旨在探讨多巴胺(DA)系统在卵巢功能中的作用,特别是在大鼠卵巢类固醇生成中的作用。经前期综合征大鼠卵巢细胞加或不加DA或其他药物孵育1小时。DA、去甲肾上腺素(NE)和异丙肾上腺素(Iso)使培养基中孕酮(P4)和cAMP水平升高。D1激动剂(SKF38393, SKF82526-J, CY208-243)增加P4分泌,而溴隐亭(D2激动剂)对介质中P4水平没有任何影响。心得安可抑制NE和Iso对P4和cAMP水平的影响(Pro;-受体阻滞剂),而由DA或D1激动剂引起的P4和cAMP水平的升高被bulbocapnine抑制(Bul;D1拮抗剂)。心得安(β受体阻滞剂)或多潘立酮(D2拮抗剂)不影响P4和cAMP水平。动力学研究揭示了经前症候群大鼠卵巢中多巴胺D1受体的存在。卵巢D1受体的最大结合位点(Bmax)为1.33fmol/mg组织,Kd值为0.357nM。这些结果提示DA系统可能通过D1受体在卵巢甾体生成中发挥生理作用。
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[The role of the dopaminergic system in the rat ovary].

Although many studies have been carried out on the dopaminergic system, little is known about the dopaminergic system in the ovary. The present study was undertaken to investigate the role of the dopamine (DA) system in ovarian function especially in steroidogenesis using rat ovaries. Ovarian cells from PMS-treated rats were incubated for 1 hour with or without DA or other drugs. DA, norepinephrine (NE) and isoproterenol (Iso) increased the levels of progesterone (P4) and cAMP in the media. D1 agonists (SKF38393, SKF82526-J, CY208-243) increased P4 secretion, whereas bromocriptine (D2 agonists) did not show any effect on the P4 level in the media. The effect of NE and Iso on P4 and cAMP levels was inhibited by propranolol (Pro; beta-blocker), while the increase of P4 and cAMP levels caused by DA or D1 agonists was suppressed by bulbocapnine (Bul; D1 antagonists). Propranolol (beta-blocker) or domperidone (D2 antagonists) did not affect the levels of P4 and cAMP. The presence of dopamine D1 receptor in the PMS-treated rat ovary was revealed by a kinetic study. The maximal number of binding sites (Bmax) of ovarian D1 receptor was 1.33fmol/mg tissue and the Kd value was 0.357nM. These results suggest that the DA system may physiologically play a role in the steroidogenesis in the ovary through D1 receptor.

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