Briley M, Chopin P, Moret C
Centre de Recherche Pierre Fabre, Castres, France.
Psychopharmacology (Berl). 1990;101(2):187-9. doi: 10.1007/BF02244124.
5,7-Dihydroxytryptamine (250 micrograms) was administered intracerebroventricularly to rats to lesion central serotonergic neurones. Fourteen days later the rats were tested in the elevated plus-maze "anxiety" model in comparison to sham lesioned animals. Twenty-four hours later, the rats were killed and serotonin levels and [3H]paroxetine binding measured in cortical and hippocampal membranes. The lesion destroyed 81% of the serotonergic innervation in the cortex and 99% in the hippocampus as determined by endogenous serotonin levels. Lesioned rats had an increased ratio of open/total arm entries in the elevated plus-maze, reflecting a decreased level of "anxiety". These results are compatible with the implication of serotonin in the control of anxiety and suggest that an anxiolytic effect may be induced by lowering the level of serotonergic activation.
向大鼠脑室内注射5,7 - 二羟基色胺(250微克)以损伤中枢5-羟色胺能神经元。14天后,与假损伤动物相比,在高架十字迷宫“焦虑”模型中对大鼠进行测试。24小时后,处死大鼠并测量皮质和海马膜中的5-羟色胺水平以及[3H]帕罗西汀结合情况。根据内源性5-羟色胺水平测定,损伤破坏了皮质中81%的5-羟色胺能神经支配和海马中99%的5-羟色胺能神经支配。损伤大鼠在高架十字迷宫中开放臂/总臂进入次数的比例增加,反映出“焦虑”水平降低。这些结果与5-羟色胺在焦虑控制中的作用相符,并表明降低5-羟色胺能激活水平可能诱导抗焦虑作用。