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促肾上腺皮质激素释放因子受体被阻断后,下丘脑阿片肽和促黄体生成素释放激素的体外和体内释放的伴随变化。

Concomitant changes in the in vitro and in vivo release of opioid peptides and luteinizing hormone-releasing hormone from the hypothalamus following blockade of receptors for corticotropin-releasing factor.

作者信息

Nikolarakis K E, Almeida O F, Sirinathsinghji D J, Herz A

机构信息

Department of Neuropharmacology, Max-Planck-Institut für Psychiatrie, Planegg-Martinsried, FRG.

出版信息

Neuroendocrinology. 1988 Jun;47(6):545-50. doi: 10.1159/000124967.

Abstract

In vitro and in vivo perfusion techniques were used to examine the changes in the release of beta-endorphin, methionine-enkephalin (met-enkephalin), dynorphin and luteinizing hormone releasing hormone (LHRH) in response to the corticotropin releasing factor (CRF) receptor antagonist, alpha-helical CRF9-41. All four peptides were measured in the same sample collected at each time interval by specific radioimmunoassay methods. In vitro release experiments were conducted using slices of hypothalami obtained from male rats whereas the in vivo release of these peptides was assessed in push-pull perfusates of the arcuate-median eminence (ARC-ME) region of the medial basal hypothalamus of chloral hydrate-anaesthetized male rats. Treatment of rat hypothalamic slices in vitro with alpha-helical CRF9-41 (10(-6) M) resulted in a significant suppression of the release of beta-endorphin and met-enkephalin within 10 min of application of the antagonist and a coincident significant increase in the release of LHRH. The levels of dynorphin were reduced but these changes were not significant. Within 10 min of withdrawal of the receptor antagonist and perfusion with normal (antagonist-free) medium the levels of these peptides returned to pretreatment values, i.e. the levels of beta-endorphin, met-enkephalin and dynorphin rose while those of LHRH fell. Comparable results were obtained in vivo during push-pull perfusion of the ARC-ME region with alpha-helical CRF9-41.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

采用体外和体内灌注技术,研究了促肾上腺皮质激素释放因子(CRF)受体拮抗剂α-螺旋CRF9-41作用下,β-内啡肽、甲硫氨酸脑啡肽(甲硫脑啡肽)、强啡肽和促黄体生成素释放激素(LHRH)释放的变化。通过特异性放射免疫测定法,在每个时间间隔采集的同一样本中测定这四种肽。体外释放实验使用从雄性大鼠获取的下丘脑切片进行,而这些肽的体内释放则在水合氯醛麻醉的雄性大鼠内侧基底下丘脑弓状-正中隆起(ARC-ME)区域的推挽灌注液中进行评估。用α-螺旋CRF9-41(10(-6) M)体外处理大鼠下丘脑切片,在应用拮抗剂后10分钟内,β-内啡肽和甲硫脑啡肽的释放受到显著抑制,同时LHRH的释放显著增加。强啡肽水平降低,但这些变化不显著。在撤去受体拮抗剂并用正常(无拮抗剂)培养基灌注10分钟内,这些肽的水平恢复到预处理值,即β-内啡肽、甲硫脑啡肽和强啡肽的水平上升,而LHRH的水平下降。在用α-螺旋CRF9-41对ARC-ME区域进行推挽灌注的体内实验中,也得到了类似的结果。(摘要截短至250字)

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