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CCKB受体激活可降低大鼠大脑皮层切片中谷氨酸诱导的去极化。

CCKB receptor activation reduces glutamate-induced depolarization in slices of rat cerebral cortex.

作者信息

Harro J, Westerling P, Oreland L

机构信息

Department of Medical Pharmacology, Uppsala University, Sweden.

出版信息

J Neural Transm Gen Sect. 1993;93(1):61-6. doi: 10.1007/BF01244938.

Abstract

Recent studies on cell cultures have indicated that the neuropeptide cholecystokinin (CCK) can prevent glutamate-induced cytotoxicity. In a preparation of rat cortical tissue placed into a two-compartment bath, the cortical tissue could be depolarized, relative to the corpus callosum, by superfusions of KCl or glutamate (1.25-10 mM). Caerulein (1-100 nM), a CCK receptor agonist, caused a rightward shift of the glutamate dose-response curve. The effect of caerulein was abolished by adding L365,260 (1 microM), a selective CCKB receptor antagonist. These findings suggest that CCK may be a physiological antagonist of glutamate-mediated neurotransmission in the rat brain.

摘要

近期关于细胞培养的研究表明,神经肽胆囊收缩素(CCK)可预防谷氨酸诱导的细胞毒性。在置于两室浴槽中的大鼠皮质组织制剂中,相对于胼胝体,通过氯化钾或谷氨酸(1.25 - 10 mM)的灌注可使皮质组织去极化。CCK受体激动剂蛙皮素(1 - 100 nM)使谷氨酸剂量反应曲线向右移动。添加选择性CCKB受体拮抗剂L365,260(1 microM)可消除蛙皮素的作用。这些发现表明,CCK可能是大鼠脑中谷氨酸介导的神经传递的生理性拮抗剂。

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