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证据表明,RF 酰胺相关肽-3 不是心理社会应激对去卵巢绵羊促性腺激素分泌抑制作用的介质。

Evidence that RF-amide related peptide-3 is not a mediator of the inhibitory effects of psychosocial stress on gonadotrophin secretion in ovariectomised ewes.

机构信息

Department of Physiology, Monash University, Victoria, Australia.

出版信息

J Neuroendocrinol. 2011 Mar;23(3):208-15. doi: 10.1111/j.1365-2826.2010.02094.x.

DOI:10.1111/j.1365-2826.2010.02094.x
PMID:21073555
Abstract

It is well known that stress inhibits normal reproductive function, including gonadotrophin secretion; however, the mechanisms and mediators involved are largely unknown. Stress impairs the secretion of luteinising hormone (LH), and it has been suggested that the RF-amide gonadotrophin-inhibitory hormone (GnIH), known as RF-amide related peptide-3 (RFRP-3) in mammalian species, may mediate this inhibitory effect of stress. If this is the case, the GnIH/RFRP system would likely be up-regulated during stress. We tested this hypothesis in ovariectomised ewes using a psychosocial stressor: isolation/restraint. Ewes were randomly allocated to control or stress (n=5 per group). Isolation/restraint stress was imposed for 90 min after control sampling for 4 h, whereas control ewes were sampled continuously for 5.5 h. All ewes were then euthanased and brains were collected. As expected, plasma concentrations of cortisol were increased significantly (P<0.05) by stress and plasma concentrations of LH were significantly (P<0.05) reduced. Immunohistochemistry and in situ hybridisation were conducted for RFRP-3 peptide and RFRP mRNA expression, respectively, in the paraventricular nucleus/dorsal medial hypothalamus region of the hypothalamus. There was no significant effect of stress on RFRP-3 peptide or mRNA levels, with no differences between control or stress ewes. Furthermore, there was no difference in the number of RFRP-3 cells double-labelled for Fos between control and stress ewes and there was no difference in the cellular expression of RFRP mRNA between groups. These results indicate that the GnIH/RFRP system is not activated by psychosocial stress in ewes, suggesting that it is an unlikely mediator of the effects of stress on LH secretion.

摘要

众所周知,压力会抑制正常的生殖功能,包括促性腺激素的分泌;然而,其中涉及的机制和介质在很大程度上仍是未知的。压力会损害黄体生成素 (LH) 的分泌,有人认为,促性腺激素抑制激素 (GnIH),即哺乳动物中的 RF 酰胺相关肽-3 (RFRP-3),可能介导了这种应激对 LH 分泌的抑制作用。如果是这样,GnIH/RFRP 系统在应激期间可能会被上调。我们使用一种心理社会应激源——隔离/束缚,在去卵巢绵羊中测试了这一假说。将绵羊随机分配到对照组或应激组(每组 5 只)。在对照组连续采样 5.5 小时后,对隔离/束缚应激组施加 90 分钟的应激。然后所有绵羊被安乐死并采集大脑。正如预期的那样,应激显著增加了皮质醇的血浆浓度(P<0.05),而 LH 的血浆浓度则显著降低(P<0.05)。分别进行了 RFRP-3 肽和 RFRP mRNA 表达的免疫组织化学和原位杂交,在下丘脑的室旁核/背内侧下丘脑区域。应激对 RFRP-3 肽或 mRNA 水平没有显著影响,对照组和应激组之间没有差异。此外,在对照组和应激组的绵羊中,Fos 双标记的 RFRP-3 细胞数量没有差异,且两组之间 RFRP mRNA 的细胞表达也没有差异。这些结果表明,GnIH/RFRP 系统不会被绵羊的心理社会应激激活,这表明它不太可能是应激对 LH 分泌影响的介导物。

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