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Dissociation Between the Aversive and Pharmacokinetic Effects of Ethanol in Female Fischer and Lewis Rats

机译:乙醇对雌性Fischer和Lewis大鼠的厌恶和药代动力学作用之间的关系

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摘要

In humans and laboratory animal models, vulnerability to alcohol abuse is influenced by endogenous factors such as genotype. Using the inbred Fischer and Lewis rat strains, we previously reported stronger conditioned taste aversions (CTA) in male Fischer rats that could not be predicted by genotypic differences in alcohol absorption []. The present study made similar assessments in Fischer and Lewis females via four-trial CTA induced by 1 or 1.5 g/kg intraperitoneal (IP) ethanol (n = 10-12/strain/dose) as well as measures of blood alcohol concentrations (BAC) at 15, 60 and 180 min post-injection with 1.5 g/kg IP ethanol or saline (n = 7-8/strain/dose). Dose-dependent CTAs were produced, but the strains did not differ from each other in these measures; however, BACs in the Lewis females were significantly higher than Fischer at all three time points. As with males of the Fischer and Lewis genotypes, a dissociation between BACs and the aversive effects of alcohol was observed. These data are the first assessments of these particular phenotypes in Fischer and Lewis females, and when considered with the historical data, suggest a Genotype × Sex interaction in the centrally-mediated sensitivity to alcohol's aversive effects.
机译:在人类和实验动物模型中,酒精滥用的易受性受内在因素(例如基因型)的影响。使用近交Fischer和Lewis大鼠品系,我们先前报道了雄性Fischer大鼠中较强的条件味厌恶(CTA),这不能通过酒精吸收的基因型差异来预测[]。本研究通过1或1.5 g / kg腹膜内(IP)乙醇(n = 10-12 /株/剂量)诱导的四次CTA对Fischer和Lewis女性进行了类似的评估,并测量了血液中的酒精浓度(BAC) ),在注射后15、60和180分钟加入1.5 g / kg IP乙醇或盐水(n = 7-8 /株/剂量)。产生了剂量依赖性的CTA,但是这些菌株在这些措施上没有差异。然而,在所有三个时间点,路易斯女性的BAC均显着高于菲舍尔。与费歇尔和刘易斯基因型的雄性一样,观察到BAC之间的解离和酒精的厌恶作用。这些数据是对费舍尔和刘易斯雌性中这些特定表型的首次评估,并且与历史数据一起考虑时,表明基因型×性别相互作用在对酒精的厌恶作用的中央介导敏感性中。

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