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慢性氯米帕明分别改变大鼠下丘脑和海马体中突触前5-羟色胺(5-HT)1B受体和突触后5-HT1A受体的敏感性。

Chronic clomipramine alters presynaptic 5-HT(1B) and postsynaptic 5-HT(1A) receptor sensitivity in rat hypothalamus and hippocampus, respectively.

作者信息

Newman M E, Gur E, Dremencov E, Garcia F, Lerer B, Van de Kar L D

机构信息

Biological Psychiatry Laboratory, Department of Psychiatry, Hadassah - Hebrew University Medical Center, PO Box 12000, 91120, Jerusalem, Israel.

出版信息

Neuropharmacology. 2000 Sep;39(12):2309-17. doi: 10.1016/s0028-3908(00)00077-0.

Abstract

Clomipramine is a tricyclic antidepressant drug with a high affinity for the serotonin (5-HT) uptake site or transporter. Electrophysiological experiments have provided evidence that repeated administration of clomipramine induces an increase in the sensitivity of postsynaptic 5-HT(1A) receptors in the hippocampus. We have studied the effects of clomipramine, administered to rats at a dose of 10mg/kg/day for 28 days by osmotic minipumps, on presynaptic 5-HT(1A) and 5-HT(1B) autoreceptors in the hypothalamus, and on postsynaptic 5-HT(1A) receptors in the hippocampus, by using in vivo microdialysis to measure 5-HT and cyclic adenosine monophosphate (cAMP) levels. Postsynaptic 5-HT(1A) receptor sensitivity in the hypothalamus was determined by means of a neuroendocrine challenge procedure. Although the sensitivity of presynaptic 5-HT(1A) autoreceptors, as measured by the effect of a subcutaneous (s.c.) injection of 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT, 0.2mg/kg or 50 microg/kg) to reduce 5-HT levels, did not change, there was a reduction in sensitivity of presynaptic 5-HT(1B) receptors, as measured by the effect of an injection of the 5-HT(1B/1D) antagonist GR 127935 (5mg/kg, s.c.) to increase 5-HT levels. This effect probably accounted for the increase in basal 5-HT levels observed in the hypothalamus after chronic clomipramine administration. Postsynaptic 5-HT(1A) receptor sensitivity in the hippocampus, measured by the effect of 8-OH-DPAT to increase cAMP levels in the dialysate, was increased after chronic clomipramine. Animals that had received daily intraperitoneal injections of 10mg/kg clomipramine for 28 days did not show a change in postsynaptic 5-HT(1A) receptor sensitivity in the hypothalamus as measured by the ability of 8-OH-DPAT (50 microg/kg, s.c.) to stimulate secretion of corticosterone. Taken together with the results of previous experiments involving the cerebral cortex, these in vivo results show that chronic clomipramine exerts effects on both pre- and postsynaptic serotonin receptors, but that these effects are highly region-specific.

摘要

氯米帕明是一种三环类抗抑郁药,对5-羟色胺(5-HT)摄取位点或转运体具有高亲和力。电生理实验已提供证据表明,重复给予氯米帕明会诱导海马体中突触后5-HT(1A)受体的敏感性增加。我们通过使用体内微透析来测量5-HT和环磷酸腺苷(cAMP)水平,研究了以10mg/kg/天的剂量通过渗透微型泵给大鼠连续注射28天氯米帕明后,其对下丘脑突触前5-HT(1A)和5-HT(1B)自身受体以及海马体中突触后5-HT(1A)受体的影响。通过神经内分泌激发程序确定下丘脑突触后5-HT(1A)受体的敏感性。尽管通过皮下(s.c.)注射8-羟基-2-(二正丙基氨基)四氢萘(8-OH-DPAT,0.2mg/kg或50μg/kg)降低5-HT水平所测得的突触前5-HT(1A)自身受体的敏感性未发生变化,但通过注射5-HT(1B/1D)拮抗剂GR 127935(5mg/kg,s.c.)增加5-HT水平所测得的突触前5-HT(1B)受体的敏感性降低。这种效应可能是慢性给予氯米帕明后下丘脑基础5-HT水平升高的原因。通过8-OH-DPAT增加透析液中cAMP水平所测得的慢性氯米帕明给药后海马体中突触后5-HT(1A)受体的敏感性增加。连续28天每天腹腔注射10mg/kg氯米帕明的动物,通过8-OH-DPAT(50μg/kg,s.c.)刺激皮质酮分泌的能力所测得的下丘脑突触后5-HT(1A)受体敏感性未发生变化。与先前涉及大脑皮层的实验结果一起,这些体内实验结果表明,慢性氯米帕明对突触前和突触后5-羟色胺受体均有影响,但这些影响具有高度的区域特异性。

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