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狂犬病病毒选择性地改变大鼠脑中的5-羟色胺1受体亚型。

Rabies virus selectively alters 5-HT1 receptor subtypes in rat brain.

作者信息

Ceccaldi P E, Fillion M P, Ermine A, Tsiang H, Fillion G

机构信息

Unité Rage, Institut Pasteur, Paris, France.

出版信息

Eur J Pharmacol. 1993 Apr 15;245(2):129-38. doi: 10.1016/0922-4106(93)90120-x.

Abstract

Rabies virus infection in man induces a series of clinical symptoms, some suggesting involvement of the central serotonergic system. The results of the present study show that, 5 days after rabies virus infection in rat, the total reversible high-affinity binding of [3H]5-HT in the hippocampus is not affected, suggesting that 5-HT1A binding is not altered. 5-HT1B sites identified by [125I]cyanopindolol binding are not affected in the cortex 3 and 5 days after the infection. Accordingly, the cellular inhibitory effect of trifluoromethylphenylpiperazine (TFMPP) on the [3H]acetylcholine-evoked release, presumably related to 5-HT1B receptor activity, is not modified 3 days after infection. In contrast, [3H]5-HT binding determined in the presence of drugs masking 5-HT1A, 5-HT1B and 5-HT1C receptors, is markedly (50%) reduced 3 days after the viral infection. These results suggest that 5-HT1D-like receptor subtypes may be affected specifically and at an early stage after rabies viral infection.

摘要

人类感染狂犬病病毒会引发一系列临床症状,其中一些症状表明中枢血清素能系统受到了影响。本研究结果显示,大鼠感染狂犬病病毒5天后,海马体中[3H]5-羟色胺的总可逆高亲和力结合不受影响,这表明5-羟色胺1A受体结合未发生改变。通过[125I]氰吲哚洛尔结合鉴定的5-羟色胺1B位点在感染后3天和5天的皮质中不受影响。因此,三氟甲基苯基哌嗪(TFMPP)对[3H]乙酰胆碱诱发释放的细胞抑制作用(可能与5-羟色胺1B受体活性有关)在感染后3天未发生改变。相比之下,在存在掩盖5-羟色胺1A、5-羟色胺1B和5-羟色胺1C受体的药物的情况下测定的[3H]5-羟色胺结合,在病毒感染后3天显著(50%)降低。这些结果表明,5-羟色胺1D样受体亚型可能在狂犬病病毒感染后早期受到特异性影响。

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