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Effects of orexins A and B on expression of orexin receptors and progesterone release in luteal and granulosa ovarian cells

机译:食欲素A和B对黄体和颗粒性卵巢细胞食欲素受体表达和孕酮释放的影响

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Orexin-A and orexin-B are neuropeptides controlling sleep-wakefulness, feeding and neuroendocrine functions via their G protein-coupled receptors, orexin-1R and orexin-2R. They are synthesized in the lateral hypothalamus and project throughout the brain. Orexins and orexin receptors have also been described outside the brain. Previously we demonstrated the presence of both receptors in the ovary, their increased expression during proestrous afternoon and the dependence on the gonadotropins.Here we studied the effects of orexins on the mRNA expression of both receptors, by quantitative real-time PCR, on luteal cells from superovulated rat ovaries and granulosa cells from diethylstilbestrol-treated rat ovaries. Effects on progesterone secretion were also measured.In luteal cells, 1. nM of either orexin-A or orexin-B decreased progesterone secretion. Orexin-A treatment increased expression of both orexin-1R and orexin-2R mRNA. The effect on orexin-1R mRNA expression was abolished by an orexin-1R selective receptor antagonist SB-334867 and the effect on orexin-2R mRNA expression was abolished by a selective orexin-2R antagonist JNJ-10397049. Orexin-B did not modify orexin-1R mRNA expression, but increased orexin-2R mRNA expression. The effect of orexin-B on orexin-2R was abolished by a selective orexin-2R antagonist. Neither the expression of orexin receptors nor progesterone secretions by granulosa cells were affected by orexins. FSH, as positive control, increased both steroid hormones secretion, but did not induce the expression of OX receptors in granulosa cells isolated from late preantral/early antral follicles. Finally in ovaries obtained immediately after sacrifice, the expression of orexin-1R and orexin-2R was higher in superovulated rat ovaries compared to control or diethylstilbestrol treated rat ovaries.A selective presence and function of both orexinergic receptors in luteal and granulosa cells is described, suggesting that the orexinergic system may have a functional role in the ovary.
机译:Orexin-A和orexin-B是通过其G蛋白偶联受体orexin-1R和orexin-2R控制睡眠觉醒,进食和神经内分泌功能的神经肽。它们在下丘脑外侧合成并投射到整个大脑。食欲素和食欲素受体也已经在脑外被描述。以前我们证明了这两种受体在卵巢中的存在,在发情的下午它们的表达增加以及对促性腺激素的依赖性。在这里,我们通过定量实时PCR研究了orexins对这两种受体的mRNA表达对黄体细胞的影响。来自超排卵的大鼠卵巢和来自己烯雌酚处理的大鼠卵巢的颗粒细胞。还测量了对孕酮分泌的影响。在黄体细胞中,1. nM的orexin-A或orexin-B降低了孕酮的分泌。 Orexin-A处理可增加orexin-1R和orexin-2R mRNA的表达。 Orexin-1R选择性受体拮抗剂SB-334867消除了对orexin-1R mRNA表达的影响,而选择性Orexin-2R拮抗剂JNJ-10397049消除了对orexin-2R mRNA表达的影响。 Orexin-B不会修饰orexin-1R mRNA表达,但会增加orexin-2R mRNA表达。选择性的orexin-2R拮抗剂消除了orexin-B对orexin-2R的作用。食欲素不影响食欲素受体的表达或颗粒细胞的孕激素分泌。 FSH作为阳性对照,增加了两种类固醇激素的分泌,但并未诱导从早期窦前/早期肛门滤泡分离出的颗粒细胞中OX受体的表达。最后,在处死后立即获得的卵巢中,与对照或己烯雌酚处理的大鼠卵巢相比,超排卵大鼠卵巢中的orexin-1R和orexin-2R的表达更高。描述了黄体和颗粒细胞中两种orexinergic受体的选择性存在和功能,提示食欲能系统可能在卵巢中发挥功能作用。

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