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促肾上腺皮质激素释放因子拮抗剂可抑制大鼠大脑局灶性脑缺血或N-甲基-D-天冬氨酸受体激活所诱导的神经元损伤。

Corticotrophin-releasing factor antagonist inhibits neuronal damage induced by focal cerebral ischaemia or activation of NMDA receptors in the rat brain.

作者信息

Strijbos P J, Relton J K, Rothwell N J

机构信息

Department of Physiological Sciences, University of Manchester, UK.

出版信息

Brain Res. 1994 Sep 12;656(2):405-8. doi: 10.1016/0006-8993(94)91485-0.

Abstract

This study investigated the involvement of corticotrophin-releasing factor (CRF) in acute neuronal damage induced by focal cerebral ischaemia or pharmacological activation of NMDA receptors in the rat brain. Intracerebroventricular injection of a CRF receptor antagonist (alpha-helical CRF9-41), markedly inhibited ischaemic (61%) and excitotoxic (41%) brain damage. Peripheral injection of a glucocorticoid antagonist (RU38486) did not affect ischaemic damage. Ischaemic and excitotoxic damage caused increased hypothalamic concentrations of CRF. These data indicate that CRF mediates ischaemic and excitotoxic neuronal damage in the rat, but that this effect is not dependent on glucocorticoids.

摘要

本研究调查了促肾上腺皮质激素释放因子(CRF)在大鼠脑局灶性脑缺血或NMDA受体药理学激活诱导的急性神经元损伤中的作用。脑室内注射CRF受体拮抗剂(α-螺旋CRF9-41)可显著抑制缺血性(61%)和兴奋性毒性(41%)脑损伤。外周注射糖皮质激素拮抗剂(RU38486)不影响缺血性损伤。缺血性和兴奋性毒性损伤导致下丘脑CRF浓度升高。这些数据表明,CRF介导大鼠的缺血性和兴奋性毒性神经元损伤,但这种作用不依赖于糖皮质激素。

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