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慢性锂治疗对大鼠脑内5-羟色胺结合位点的影响。

Effects of chronic lithium treatment on serotonin binding sites in rat brain.

作者信息

Odagaki Y, Koyama T, Matsubara S, Matsubara R, Yamashita I

机构信息

Department of Psychiatry and Neurology, Hokkaido University School of Medicine, Sapporo, Japan.

出版信息

J Psychiatr Res. 1990;24(3):271-7. doi: 10.1016/0022-3956(90)90016-j.

Abstract

The effects of lithium treatment on serotonin (5-HT) binding sites in the rat brain were investigated. Oral administration of lithium carbonate for 3 weeks did not influence 5-HT2 binding sites in the cerebral cortex. On the other hand, the number of 5-HT1 binding sites labeled with [3H]5-HT was decreased significantly in the hippocampus, but not in the cerebral cortex. While non-5-HT1A sites, defined as specific [3H]5-HT binding in the presence of 100 nM 8-hydroxy-2-(di-n-propylamino) tetralin (8-OH-DPAT), were not affected by lithium treatment in either brain region, chronic lithium administration reduced significantly the density of 5-HT1A sites labeled with [3H]8-OH-DPAT only in the hippocampus, but not in the cerebral cortex. These results suggest that 5-HT1A components are responsible for lithium-induced down-regulation of 5-HT1 binding sites in the hippocampus and that 5-HT1A sites in the hippocampus might be connected with the therapeutic efficacy of lithium.

摘要

研究了锂治疗对大鼠脑内5-羟色胺(5-HT)结合位点的影响。口服碳酸锂3周对大脑皮质中的5-HT2结合位点没有影响。另一方面,用[3H]5-HT标记的5-HT1结合位点数量在海马体中显著减少,但在大脑皮质中未减少。虽然在100 nM 8-羟基-2-(二正丙基氨基)四氢萘(8-OH-DPAT)存在下定义为特异性[3H]5-HT结合的非5-HT1A位点在两个脑区均不受锂治疗的影响,但长期给予锂仅显著降低了海马体中用[3H]8-OH-DPAT标记的5-HT1A位点的密度,而大脑皮质中未降低。这些结果表明,5-HT1A成分是锂诱导海马体中5-HT1结合位点下调的原因,并且海马体中的5-HT1A位点可能与锂的治疗效果有关。

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