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谷氨酸通过α受体诱导促黄体生成素释放激素释放。

Glutamic acid induces luteinizing hormone releasing hormone release via alpha receptors.

作者信息

Kamat A, Yu W H, Rettori V, McCann S M

机构信息

Department of Physiology, University of Texas Southwestern Medical Center at Dallas 75235-8873, USA.

出版信息

Brain Res Bull. 1995;37(3):233-5. doi: 10.1016/0361-9230(94)00280-e.

Abstract

Glutamic acid (GA) and norepinephrine (NE) stimulate luteinizing hormone-releasing hormone (LHRH) release via release of nitric oxide (NO) from NOergic neurons in the arcuate-median eminence region. To determine if GA releases LHRH via direct stimulation of NOergic neurons, or via stimulation of noradrenergic terminals, arcuate median eminence explants from male rats were incubated with various compounds, and the LHRH release into the medium was measured. GA-induced release of LHRH was completely blocked by phentolamine (1 microM), an alpha receptor blocker, which, by itself, had no effect on the release. Nitroprusside (NP), which spontaneously releases NO, more than doubled LHRH release. To determine if alpha receptors on the LHRH neuron are required for the action of NP, the tissue was incubated with phentolamine, plus NP. Phentolamine had no effect on the LHRH-releasing action of NP. The results are interpreted to mean that GA activates the release of NE from the noradrenergic terminals. This acts on alpha receptors on the NOergic neuron to produce the release of NO. This NO diffuses to the LHRH terminals and induces release of LHRH.

摘要

谷氨酸(GA)和去甲肾上腺素(NE)通过弓状正中隆起区域的一氧化氮(NO)能神经元释放一氧化氮(NO)来刺激促黄体生成素释放激素(LHRH)的释放。为了确定GA是通过直接刺激NO能神经元还是通过刺激去甲肾上腺素能终末来释放LHRH,将雄性大鼠的弓状正中隆起外植体与各种化合物一起孵育,并测量释放到培养基中的LHRH。GA诱导的LHRH释放被α受体阻滞剂酚妥拉明(1 microM)完全阻断,而酚妥拉明本身对释放没有影响。自发释放NO的硝普钠(NP)使LHRH释放增加了一倍多。为了确定NP的作用是否需要LHRH神经元上的α受体,将组织与酚妥拉明和NP一起孵育。酚妥拉明对NP的LHRH释放作用没有影响。结果表明,GA激活去甲肾上腺素能终末释放NE。这作用于NO能神经元上的α受体以产生NO的释放。这种NO扩散到LHRH终末并诱导LHRH的释放。

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