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Arg-Phe-amide 相关肽影响促性腺激素释放激素神经元。

Arg-Phe-amide-related peptides influence gonadotropin-releasing hormone neurons.

机构信息

Department of Physiology, Medical School, Firat University, Elazig, Turkey.

Department of Biochemistry, Medical School, Karadeniz Technical University, Elazig, Turkey.

出版信息

Neural Regen Res. 2013 Jun 25;8(18):1714-20. doi: 10.3969/j.issn.1673-5374.2013.18.009.

Abstract

The hypothalamic Arg-Phe-amide-related peptides, gonadotropin-inhibitory hormone and orthologous mammalian peptides of Arg-Phe-amide, may be important regulators of the hypothalamus-pituitary-gonadal reproductive axis. These peptides may modulate the effects of kisspeptins because they are presently recognized as the most potent activators of the hypothalamus-pituitary-gonadal axis. However, their effects on gonadotropin-releasing hormone neurons have not been investigated. In the current study, the GT1-7 cell line-expressing gonadotropin-releasing hormone was used as a model to explore the effects of Arg-Pheamide-related peptides on kisspeptin activation. Intracellular calcium concentration was quantified using the calcium-sensitive dye, fura-2 acetoxymethyl ester. Gonadotropin-releasing hormone released into the medium was detected via enzyme-linked immunosorbent assay. Results showed that 100 nmol/L kisspeptin-10 significantly increased gonadotropin-releasing hormone levels (at 120 minutes of exposure) and intracellular calcium concentrations. Co-treatment of kisspeptin with 1 μmol/L gonadotropin-inhibitory hormone or 1 μmol/L Arg-Phe-amide-related peptide-1 significantly attenuated levels of kisspeptin-induced gonadotropin-releasing hormone but did not affect kisspeptin-induced elevations of intracellular calcium concentration. Overall, the results suggest that gonadotropin-inhibitory hormone and Arg-Phe-amide-related peptide-1 may have inhibitory effects on kisspeptin-activated gonadotropin-releasing hormone neurons independent of the calcium signaling pathway.

摘要

下丘脑的 Arg-Phe-amide 相关肽、促性腺激素抑制激素和 Arg-Phe-amide 的同源哺乳动物肽可能是下丘脑-垂体-性腺生殖轴的重要调节因子。这些肽可能调节 kisspeptin 的作用,因为它们目前被认为是下丘脑-垂体-性腺轴的最有效激活剂。然而,它们对促性腺激素释放激素神经元的影响尚未得到研究。在当前的研究中,表达促性腺激素释放激素的 GT1-7 细胞系被用作模型,以探讨 Arg-Phe-amide 相关肽对 kisspeptin 激活的影响。使用钙敏感染料 fura-2 乙氧基甲酯定量测量细胞内钙浓度。通过酶联免疫吸附试验检测到释放到培养基中的促性腺激素释放激素。结果表明,100 nmol/L kisspeptin-10 显著增加了促性腺激素释放激素水平(在暴露 120 分钟时)和细胞内钙浓度。 kisspeptin 与 1 μmol/L 促性腺激素抑制激素或 1 μmol/L Arg-Phe-amide 相关肽-1 共同处理显著减弱了 kisspeptin 诱导的促性腺激素释放激素水平,但不影响 kisspeptin 诱导的细胞内钙浓度升高。总体而言,这些结果表明,促性腺激素抑制激素和 Arg-Phe-amide 相关肽-1 可能对 kisspeptin 激活的促性腺激素释放激素神经元具有抑制作用,而不依赖于钙信号通路。

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