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MDL 73,147EF,一种5-羟色胺3拮抗剂,可促进大鼠的潜在抑制。

MDL 73,147EF, a 5-HT3 antagonist, facilitates latent inhibition in the rat.

作者信息

Moran P M, Moser P C

机构信息

Marion Merrell Dow Research Institute, Strasbourg, France.

出版信息

Pharmacol Biochem Behav. 1992 Jul;42(3):519-22. doi: 10.1016/0091-3057(92)90148-9.

Abstract

Latent inhibition (LI) is a behavioral model of selective attention that has been used to study the attentional deficits seen in schizophrenia. In the present study, we examined the effect of 5-hydroxytryptamine3 (5-HT3) receptor blockade on LI using the conditioned emotional response (CER) procedure. Prior exposure to 20, 30, or 40 stimulus presentations significantly, and almost completely, inhibited the CER to that stimulus. This LI effect was much weaker when only 10 preexposures were given. 1H-indole-3-carboxylic acid, trans-octahydro-3-oxo-2,6-methano-2H-quinolizin-8-yl ester methanesulfonate (MDL 73,147EF), a selective 5-HT3 receptor antagonist, significantly facilitated the LI effect observed after 10 preexposures at 0.1 mg/kg but not at 0.01 mg/kg. The magnitude of this effect was comparable to that observed with the classical neuroleptic haloperidol (0.1 mg/kg). Neither MDL 73,147EF nor haloperidol affected the CER in animals not preexposed to the stimulus. These results strongly corroborate suggestions that 5-HT3 receptor antagonists will be of use in the treatment of schizophrenia.

摘要

潜伏抑制(LI)是一种选择性注意的行为模型,已被用于研究精神分裂症中出现的注意力缺陷。在本研究中,我们使用条件性情绪反应(CER)程序研究了5-羟色胺3(5-HT3)受体阻断对LI的影响。事先接触20次、30次或40次刺激会显著且几乎完全抑制对该刺激的CER。当只进行10次预接触时,这种LI效应要弱得多。1H-吲哚-3-羧酸,反式八氢-3-氧代-2,6-亚甲基-2H-喹嗪-8-基酯甲磺酸盐(MDL 73,147EF),一种选择性5-HT3受体拮抗剂,在0.1mg/kg时能显著促进10次预接触后观察到的LI效应,但在0.01mg/kg时则不能。这种效应的程度与经典抗精神病药物氟哌啶醇(0.1mg/kg)观察到的相当。MDL 73,147EF和氟哌啶醇均未影响未事先接触该刺激的动物的CER。这些结果有力地证实了5-HT3受体拮抗剂将可用于治疗精神分裂症的观点。

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