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长期锂治疗通过大鼠脑中的血清素能突触前膜导致血清素受体下调。

Long-term lithium treatment causes serotonin receptor down-regulation via serotonergic presynapses in rat brain.

作者信息

Hotta I, Yamawaki S, Segawa T

出版信息

Neuropsychobiology. 1986;16(1):19-26. doi: 10.1159/000118292.

Abstract

The effects of lithium treatment on serotonin (5-HT) receptors in rat frontal cortex and hippocampus were investigated. Long-term lithium treatment strongly blocked 5-hydroxytryptophan-induced head twitches, while acute lithium administration by itself induced head twitches in rats, and ketanserin blocked this acute lithium action. Long-term administration of lithium decreased the number of not only 5-HT2 receptors in the frontal cortex but also 5-HT1 and 5-HT2 receptors in the hippocampus in rats. Decreases in 3H-5-HT binding to hippocampal 5-HT1 receptors and 3H-spiperone binding to frontal cortical 5-HT2 receptors, caused by chronic lithium treatment, were abolished by co-administration of p-chlorophenylalanine, and were enhanced by co-administration with methiothepin. The turnover of 5-HT in either frontal cortex or hippocampus was facilitated by lithium, and co-administered methiothepin enhanced this facilitation. These results suggest that long-term lithium treatment causes the down-regulation of postsynaptic 5-HT1 and 5-HT2 receptors, in part probably through its action on presynaptic nerve terminals.

摘要

研究了锂治疗对大鼠额叶皮质和海马中5-羟色胺(5-HT)受体的影响。长期锂治疗强烈阻断5-羟色氨酸诱导的头部抽搐,而急性给予锂本身会在大鼠中诱导头部抽搐,酮色林可阻断这种急性锂作用。长期给予锂不仅会减少大鼠额叶皮质中5-HT2受体的数量,还会减少海马中5-HT1和5-HT2受体的数量。慢性锂治疗导致的海马5-HT1受体的3H-5-HT结合以及额叶皮质5-HT2受体的3H-螺哌隆结合的减少,通过联合给予对氯苯丙氨酸而被消除,并通过与甲硫噻平联合给药而增强。锂促进额叶皮质或海马中5-HT的周转,联合给予的甲硫噻平增强了这种促进作用。这些结果表明,长期锂治疗会导致突触后5-HT1和5-HT2受体的下调,部分原因可能是其对突触前神经末梢的作用。

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