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Pharmacologically relevant intake during chronic, free-choice drinking rhythms in selectively bred high alcohol-preferring mice

机译:选择性高酒精偏爱小鼠的慢性,自由选择的饮酒节律期间的药理学相关摄入

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Multiple lines of high alcohol-preferring (HAP) mice were selectively bred for their intake of 10% ethanol (v/v) during 24-hour daily access over a 4-week period, with the highest drinking lines exhibiting intakes in excess of 20 g/kg/day. We observed circadian drinking patterns and resulting blood ethanol concentrations (BECs) in the HAP lines. We also compared the drinking rhythms and corresponding BECs of the highest drinking HAP lines to those of the C57BL/6J (B6) inbred strain. Adult male and female crossed HAP (cHAP), HAP replicate lines 1, 2, 3 and B6 mice had free-choice access to 10% ethanol and water for 3 weeks prior to bi-hourly assessments of intake throughout the dark portion of the light-dark cycle. All HAP lines reached and maintained a rate of alcohol intake above the rate at which HAP1 mice metabolize alcohol, and BECs were consistent with this finding. Further, cHAP and HAP1 mice maintained an excessive level of intake throughout the dark portion of the cycle, accumulating mean BEC levels of 261.5 ± 18.09 and 217.9 ± 25.02 mg/dl, respectively. B6 mice drank comparatively modestly, and did not accumulate high BEC levels (53.63 + 8.15 mg/dl). Free-choice drinking demonstrated by the HAP1 and cHAP lines may provide a unique opportunity for modeling the excessive intake that often occurs in alcohol-dependent individuals, and allow for exploration of predisposing factors for excessive consumption, as well as the development of physiological, behavioral and toxicological outcomes following alcohol exposure.
机译:在4周的每日24小时访问期间,多头高酒精偏爱(HAP)小鼠系选择性繁殖了10%乙醇(v / v)的摄入量,其中最高饮水量的摄入量超过20克/千克/天。我们观察了HAP品系中的昼夜节律饮酒模式和所产生的血液乙醇浓度(BEC)。我们还比较了最高饮水HAP品系与C57BL / 6J(B6)自交系的饮水节奏和相应的BEC。成年雄性和雌性杂交HAP(cHAP),HAP复制品系1、2、3和B6小鼠可以自由选择10%的乙醇和水3周,然后每两小时评估整个黑暗部分的摄入量-黑暗的周期。所有HAP品系均达到并维持酒精摄入速率,高于HAP1小鼠代谢酒精的速率,而BEC与这一发现一致。此外,cHAP和HAP1小鼠在整个周期的黑暗部分都保持摄入过多水平,分别累积了平均BEC水平261.5±18.09和217.9±25.02 mg / dl。 B6小鼠喝适度,并且没有积累高BEC水平(53.63 + 8.15 mg / dl)。由HAP1和cHAP品系证明的自由选择饮酒可能提供了一个独特的机会来模拟酒精依赖型个体中经常发生的过量摄入,并允许探索过量摄入的诱发因素,以及生理,行为和行为的发展。和酒精接触后的毒理学结果。

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