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大鼠海马切片中CB1大麻素受体的激活会抑制钾离子诱发的胆囊收缩素释放,这可能是大麻素导致空间记忆缺陷的一种机制。

Activation of CB1 cannabinoid receptors in rat hippocampal slices inhibits potassium-evoked cholecystokinin release, a possible mechanism contributing to the spatial memory defects produced by cannabinoids.

作者信息

Beinfeld M C, Connolly K

机构信息

Department of Pharmacology and Experimental Therapeutics, Tufts University School of Medicine, 136 Harrison Avenue, Boston, MA 02111, USA.

出版信息

Neurosci Lett. 2001 Mar 23;301(1):69-71. doi: 10.1016/s0304-3940(01)01591-9.

Abstract

Cannabinoid use is known to disrupt learning and memory in a number of species. cholecystokinin (CCK) release and CCK receptors have been implicated in spatial memory processes in rodents. Rat hippocampal CCK interneurons express cannabinoid 1 receptors (CB1). The CB1 agonist R(+)WIN 55,212-2 (WIN+), at 1 and 10 micromol, strongly inhibited potassium-evoked CCK release from rat hippocampal slices, while the inactive isomer S(-)WIN,55,212-3 (WIN-) had no effect. CCK release from cerebral cortical slices was not altered by WIN+.

摘要

已知使用大麻素会干扰多种物种的学习和记忆。胆囊收缩素(CCK)的释放及CCK受体与啮齿动物的空间记忆过程有关。大鼠海马体CCK中间神经元表达大麻素1型受体(CB1)。CB1激动剂R(+)WIN 55,212-2(WIN+),浓度为1和10微摩尔时,强烈抑制钾离子诱发的大鼠海马体切片中CCK的释放,而无活性的异构体S(-)WIN 55,212-3(WIN-)则无此作用。WIN+不会改变大脑皮质切片中CCK的释放。

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