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抗抑郁药对大鼠大脑皮层去甲肾上腺素摄取和释放的影响。

Effects of antidepressants on the uptake and release of norepinephrine from rat cerebral cortex.

作者信息

Rubinstein-Kawamoto J, Davis J M, Pandey G N

出版信息

Psychopharmacology (Berl). 1984;84(2):155-7. doi: 10.1007/BF00427438.

Abstract

The effects of several antidepressants on the release of (3H)-norepinephrine (NE) from homogenates of rat cerebral cortex were studied. A continuous superfusion collection system was used in order to differentiate these effects from effects on reuptake. Amitriptyline, maprotiline, mianserin, and trazodone produced a statistically significant decrease in spontaneous tritium efflux when present in the superfusion medium at a concentration of 1.0 microM. The other antidepressants studied had no effect. We used a buffer with the K+ concentration raised to 56 mM as a model of depolarization-induced release. Desipramine, fluoxetine, and iprindole (again at 1.0 microM) caused a significant decrease in this measure. These results indicate that some of both the tricyclic and atypical antidepressants may alter spontaneous or depolarization-induced release of NE.

摘要

研究了几种抗抑郁药对大鼠大脑皮层匀浆中(3H)-去甲肾上腺素(NE)释放的影响。为了将这些影响与对再摄取的影响区分开来,使用了连续超灌注收集系统。当阿米替林、马普替林、米安色林和曲唑酮以1.0微摩尔/升的浓度存在于超灌注培养基中时,它们会使自发氚流出量出现统计学上的显著下降。所研究的其他抗抑郁药则没有效果。我们使用钾离子浓度提高到56毫摩尔/升的缓冲液作为去极化诱导释放的模型。地昔帕明、氟西汀和茚满二氮卓(同样为1.0微摩尔/升)使这一指标显著下降。这些结果表明,一些三环类和非典型抗抑郁药可能会改变NE的自发或去极化诱导释放。

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