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Alterations in Ethanol Seeking and Self-Administration Following Yohimbine in Selectively Bred Alcohol-Preferring (P) and High Alcohol Drinking (HAD-2) Rats

机译:在选择性地培养育醇偏好(P)和高级酒精(HAD-2)大鼠中乙醇寻求和自我管理改变

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摘要

Evidence suggests that stress increases alcohol drinking and promotes relapse in humans. Animal models that assess related behaviors include the sipper tube ethanol self-administration and the stress-induced reinstatement paradigms. While selectively bred for the same high-ethanol-drinking behavior, alcohol-preferring P rats appear to show greater sensitivity to ethanol reinforcement than high-alcohol-drinking HAD rats. The present experiment tested the effects of the pharmacological stressor, yohimbine, on the motivation to seek and consume ethanol implementing a combined sipper tube/reinstatement model using male P and HAD-2 rats. Following training to self-administer ethanol using the sipper tube procedure, rats were tested for the effects of yohimbine (0.625-2.5 mg/kg) on ethanol drinking. Subsequently, rats were tested for the effects of 1.25 mg/kg yohimbine on reinstatement of ethanol seeking. Yohimbine (0.625 and 1.25 mg/kg) increased ethanol self-administration, and the latter dose also decreased latency to complete the response requirement. Yohimbine elicited reinstatement of ethanol seeking in both lines. HAD-2 rats drank more ethanol, but showed similar responding on the ethanol-associated lever compared to P rats. These findings extend both the reinstatement and sipper tube models and justify further exploration of this unique combined paradigm. Despite prior evidence suggesting that P rats are more motivated to seek and consume ethanol, differences in these behaviors between P and HAD-2 rats were not systematic in the present experiment. Further investigation may elucidate whether either selected line may be more sensitive than other selectively bred or outbred rats to stress-related changes in ethanol's reinforcing effects.
机译:有证据表明,压力会增加饮酒量并促进人类复发。评估相关行为的动物模型包括吸管乙醇自我管理和应激诱导的恢复范例。尽管针对相同的高乙醇饮用行为进行了选择性繁殖,但偏爱酒精的P大鼠似乎对乙醇强化的敏感性高于高喝酒精的HAD大鼠。本实验使用雄性P和HAD-2大鼠,通过组合吸管/修复模型,测试了药理应激源育亨宾对寻求和消耗乙醇的动机的影响。在使用吸管程序自我训练乙醇训练后,测试了大鼠育亨宾(0.625-2.5 mg / kg)对饮酒的影响。随后,测试了大鼠1.25 mg / kg育亨宾对恢复寻找乙醇的作用。育亨宾(0.625和1.25 mg / kg)增加了乙醇的自我给药,而后者的剂量也减少了潜伏期以完成反应要求。育亨宾引发了这两种品系中乙醇寻找的恢复。 HAD-2大鼠喝更多的乙醇,但与P大鼠相比,在乙醇相关的杠杆上显示出相似的反应。这些发现扩展了修复和吸管模型,并证明了对该独特组合范例的进一步探索。尽管已有证据表明,P大鼠更容易寻求和消耗乙醇,但在本实验中,P和HAD-2大鼠之间的这些行为差异并不系统。进一步的研究可以阐明,任一选择的品系是否可能比其他选择性繁殖或近交的大鼠对乙醇增强作用中与应激相关的变化更为敏感。

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