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5-羟色胺1A受体拮抗剂对大鼠强迫游泳试验中8-羟基二丙胺、丁螺环酮和地昔帕明抗抑郁样作用的阻断。

Blockade of the antidepressant-like effects of 8-OH-DPAT, buspirone and desipramine in the rat forced swim test by 5HT1A receptor antagonists.

作者信息

Detke M J, Wieland S, Lucki I

机构信息

Department of Psychology, University of Pennsylvania, Philadelphia 19104-6196, USA.

出版信息

Psychopharmacology (Berl). 1995 May;119(1):47-54. doi: 10.1007/BF02246053.

Abstract

This study examined whether the antidepressant-like effect of serotonin (5-HT)1A receptor agonists in the forced swim test (FST) is mediated by 5-HT1A receptors. The 5-HT1A receptor agonists 8-hydroxy-2-(di-n-propylamino) tetralin (8-OH-DPAT) and buspirone decreased immobility in the FST. The effect of 8-OH-DPAT was blocked by the 5-HT1A receptor antagonists NAN 190, BMY 7378 and pindolol. The effect of buspirone was blocked by NAN 190 and pindolol. The antagonists produced no effects on their own. The norepinephrine (NE) uptake inhibitor desipramine (DMI) also reduced immobility, and this was also blocked by NAN 190, BMY 7378 and pindolol. The alpha 1, beta 1 and beta 2 adrenergic antagonists prazosin, betaxolol and ICI 118,551 did not block either 8-OH-DPAT or DMI, and produced no effects on their own. These results provide evidence that the antidepressant-like effects of 5-HT1A receptor agonists in the FST are mediated through 5-HT1A receptors, probably located postsynaptically. The finding that the 5-HT1A receptor antagonists blocked the effect of DMI suggests that the NE and 5-HT systems interact in the FST.

摘要

本研究检测了血清素(5-羟色胺,5-HT)1A受体激动剂在强迫游泳试验(FST)中的抗抑郁样效应是否由5-HT1A受体介导。5-HT1A受体激动剂8-羟基-2-(二正丙基氨基)四氢萘(8-OH-DPAT)和丁螺环酮可减少FST中的不动时间。8-OH-DPAT的效应被5-HT1A受体拮抗剂NAN 190、BMY 7378和吲哚洛尔阻断。丁螺环酮的效应被NAN 190和吲哚洛尔阻断。这些拮抗剂自身无作用。去甲肾上腺素(NE)摄取抑制剂地昔帕明(DMI)也可减少不动时间,且同样被NAN 190、BMY 7378和吲哚洛尔阻断。α1、β1和β2肾上腺素能拮抗剂哌唑嗪、倍他洛尔和ICI 118,551既不阻断8-OH-DPAT也不阻断DMI,且自身无作用。这些结果证明,5-HT1A受体激动剂在FST中的抗抑郁样效应是通过可能位于突触后的5-HT1A受体介导的。5-HT1A受体拮抗剂阻断DMI效应这一发现表明,NE和5-HT系统在FST中相互作用。

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