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Growth hormone-releasing hormone activates sleep regulatory neurons of the rat preoptic hypothalamus

机译:生长激素释放激素激活大鼠视前下丘脑的睡眠调节神经元

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摘要

We examined whether growth hormone-releasing hormone (GHRH) may promote non-rapid eye movement (NREM) sleep via activation of GABAergic neurons in the preoptic area. Male Sprague-Dawley rats were implanted with EEG, EMG electrodes and a unilateral intracerebroventricular cannula. Groups of rats received injections (3 μl icv) with gonadotropin-releasing hormone (GHRH) (0.1 nmol/100 g body wt) or equal volume of physiological saline at the onset of the dark period and were permitted spontaneous sleep for 90 min. Separate groups of rats were sleep deprived by gentle handling for 90 min, beginning at the time of GHRH or saline injection, at the onset of the dark period. Other groups of rats received intracerebroventricular octreotide (somatostatin analog OCT) injections, intracerebroventricular injection of one of two doses of competitive GHRH antagonist, or intracerebroventricular saline injection at light onset and were then permitted 90 min spontaneous sleep-waking. Rats were killed immediately after the 90-min sleep/wake monitoring period. Brain tissue was processed for immunohistochemistry for c-Fos protein and glutamic acid decarboxylase (GAD). Single c-Fos and dual Fos-GAD cell counts were determined in the median preoptic nucleus (MnPN), and in the core and the extended parts of the ventrolateral preoptic nucleus (cVLPO and exVLPO). Intracerebroventricular GHRH elicited a significant increase in NREM sleep amount. Double-labeled Fos+GAD cell counts were significantly elevated after GHRH injection in the MnPN and VLPO in both undisturbed and sleep-deprived groups. OCT and GHRH antagonist significantly decreased NREM sleep amount compared with control rats. OCT injection increased single c-Fos-labeled cell counts in the MnPN, but not in the VLPO. Double-labeled cell counts were significantly reduced after OCT and the high dose of GHRH antagonist injection in all areas examined. These findings identify GABAergic neurons in the MnPN and VLPO as potential targets of the sleep-regulatory actions of GHRH.
机译:我们检查了生长激素释放激素(GHRH)是否可以通过激活视前区GABA能神经元来促进非快速眼动(NREM)睡眠。将雄性Sprague-Dawley大鼠植入EEG,EMG电极和单侧脑室插管。在黑暗期开始时,各组大鼠接受注射促性腺激素释放激素(GHRH)(0.1 nmol / 100 g体重)或等体积生理盐水的注射(3μlicv),并允许自发睡眠90分钟。从GHRH或生理盐水注射开始,在黑暗时期开始,通过温和的处理剥夺单独的大鼠组睡眠90分钟。其他组的大鼠在轻度发作时接受脑室内奥曲肽(somatostatin类似物OCT)注射,脑室内注射两种剂量的竞争性GHRH拮抗剂之一或脑室内盐水注射,然后允许90分钟自觉醒来。在90分钟的睡眠/觉醒监测期后立即杀死大鼠。对脑组织进行了c-Fos蛋白和谷氨酸脱羧酶(GAD)的免疫组织化学处理。在中位视前核(MnPN)以及腹侧前视核的核心和延伸部分(cVLPO和exVLPO)确定单c-Fos和双Fos-GAD细胞计数。脑室内GHRH引起NREM睡眠量显着增加。 GHPN注射后,未干扰组和睡眠剥夺组的MnPN和VLPO中双标记的Fos + GAD细胞计数均显着升高。与对照组相比,OCT和GHRH拮抗剂显着降低了NREM睡眠量。 OCT注射增加了MnPN中单个c-Fos标记的细胞计数,但VLPO中没有。在所有检查的区域中,OCT和高剂量的GHRH拮抗剂注射后,双标记细胞计数显着降低。这些发现确定了MnPN和VLPO中的GABA能神经元是GHRH睡眠调节作用的潜在靶标。

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