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在成年早期而非青春期早期给予σ-1受体激动剂PRE-084,可减轻雌性大鼠乙醇诱导的条件性味觉厌恶。

Administration of the sigma-1 receptor agonist PRE-084 at emerging adulthood, but not at early adolescence, attenuated ethanol-induced conditioned taste aversion in female rats.

作者信息

Salguero Agustín, Marengo Leonardo, Portillo-Salido Enrique, Ruiz-Leyva Leandro, Cendán Cruz Miguel, Morón Ignacio, Marcos Pautassi Ricardo

机构信息

Instituto de Investigación Médica M. y M. Ferreyra (INIMEC-CONICET-Universidad Nacional de Córdoba), Córdoba C.P. 5000, Argentina.

WELAB Barcelona, Parc Científic de Barcelona, C/Baldiri Reixac 4-8, 08028 Barcelona, Spain.

出版信息

Neurosci Lett. 2022 May 1;778:136585. doi: 10.1016/j.neulet.2022.136585. Epub 2022 Mar 19.

Abstract

Ethanol-induced conditioned taste aversion (CTA) is greater in late adolescence or young adulthood than in early adolescence. The role of the sigma receptor system in this age-related difference has not been extensively explored, particularly in female rats. This study assessed the effects of the activation of sigma-1 receptors (S1-R), via the selective S1-R agonist PRE-084, on ethanol-induced CTA at early or at terminal adolescence/emerging adulthood (28 or 56 days-old at the beginning of the procedures, respectively) in female Wistar rats. The modulation of binge-like ethanol intake by PRE-084 was assessed at terminal adolescence. S1-R activation at the acquisition of ethanol-induced CTA attenuated such learning at terminal but not at early adolescence. PRE-084 did not significantly affect ethanol binge drinking in the terminal adolescents. These results highlight the role of S1-R in ethanol-induced CTA and suggest that differential functionality of this transmitter system may underlie age-specific sensitivities to the aversive effects of ethanol.

摘要

乙醇诱导的条件性味觉厌恶(CTA)在青春期末期或成年早期比青春期早期更强烈。西格玛受体系统在这种与年龄相关的差异中所起的作用尚未得到广泛研究,尤其是在雌性大鼠中。本研究评估了通过选择性西格玛-1受体(S1-R)激动剂PRE-084激活S1-R对雌性Wistar大鼠青春期早期或青春期末期/成年初期(实验开始时分别为28或56日龄)乙醇诱导的CTA的影响。在青春期末期评估PRE-084对类似暴饮暴食的乙醇摄入量的调节作用。在乙醇诱导的CTA习得时激活S1-R可在青春期末期而非青春期早期减弱这种学习。PRE-084对青春期末期大鼠的乙醇暴饮没有显著影响。这些结果突出了S1-R在乙醇诱导的CTA中的作用,并表明该递质系统的不同功能可能是对乙醇厌恶效应的年龄特异性敏感性的基础。

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