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Complex interactions between the subject factors of biological sex and prior histories of binge-drinking and unpredictable stress influence behavioral sensitivity to alcohol and alcohol intake

机译:生物性别的主体因素与狂欢饮酒和不可预测的压力的现有历史之间的复杂相互作用会影响对酒精和酒精摄入量的行为敏感性

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Alcohol use disorders, affective disorders and their comorbidity are sexually dimorphic in humans. However, it is difficult to disentangle the interactions between subject factors influencing alcohol sensitivity in studies of humans. Herein, we combined murine models of unpredictable, chronic, mild stress (UCMS) and voluntary binge-drinking to examine for sex differences in the interactions between prior histories of excessive ethanol drinking and stress upon ethanol-induced changes in motor behavior and subsequent drinking. In Experiment 1, female mice were insensitive to the UCMS-induced increase in ethanol-induced locomotion and ethanol intake under continuous alcohol-access. Experiment 2 revealed interactions between ethanol dose and sex (females > males), binge-drinking history (water > ethanol), and UCMS history (UCMS > controls), with no additive effect of a sequential prior history of both binge drinking and UCMS observed. We also observed an interaction between UCMS history and sex for righting recovery. UCMS history potentiated subsequent binge drinking in water controls of both sexes and in male binge-drinking mice. Conversely, a prior binge-drinking history increased subsequent ethanol intake in females only, irrespective of prior UCMS history. In Experiment 3, a concurrent history of binge-drinking and UCMS did not alter ethanol intake, nor did it influence the ethanol dose-locomotor response function, but it did augment alcohol-induced sedation and reduced subsequent alcohol intake over that produced by binge-drinking alone. Thus, the subject factors of biological sex, prior stressor history and prior binge-drinking history interact in complex ways in mice to impact sensitivity to alcohol's motor-stimulating,-incoordinating and intoxicating effects, as well as to influence subsequent heavy drinking.
机译:酒精使用障碍,情感障碍及其合并症是人类的性二态。然而,难以解除影响人类研究中的酒精敏感性的受试者因素之间的相互作用。在此,我们将鼠模型联合不可预测,慢性,轻度(UCMS)和自愿狂犬病饮用的鼠模型,以检查现有乙醇饮用和乙醇诱导的运动行为变化和随后饮用后的过量乙醇饮用和胁迫之间的相互作用的性差异。在实验1中,雌性小鼠对连续醇类进入的乙醇诱导的运动诱导的运动诱导的运动和乙醇摄入不敏感。实验2揭示了乙醇剂量和性别(女性>雄性),泪流的历史(水>乙醇)和UCMS历史(UCMS>对照)之间的相互作用,没有任何夸张饮用和UCM的顺序历史的添加剂效应。我们还观察到UCMS历史和性别之间的互动,以便妥善恢复。 UCMS病史有助于随后的狂犬病饮用,在两性和雄性狂潮小鼠的水控制中饮用。相反,无论先前的UCMS历史如何,都会增加先前的狂犬病饮酒历史,随后只增加了女性的乙醇摄入量。在实验3中,泪流的饮用和ucms的并发历史并未改变乙醇摄入,也没有影响乙醇剂量 - 运动反应功能,但它确实增强了醇诱导的镇静并降低了由狂暴产生的随后的酒精摄入量减少 - 独自喝酒。因此,生物性别的主题因素,先前的压力源史和先前的泪流饮酒历史以大鼠的复杂方式相互作用,以影响醇的运动刺激, - 互动和令人陶醉的效果的敏感性,以及影响随后的重饮用。

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