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Reduced sensitivity to ethanol and excessive drinking in a mouse model of neuropathic pain

机译:降低对乙醇的敏感性,并在神经病疼痛的小鼠模型中过度饮用

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Abstract The co‐occurrence of chronic pain and alcohol use disorders (AUDs) involves complex interactions between genetic and neurophysiological aspects, and the research has reported mixed findings when they both co‐occur. There is also an indication of a gender‐dependent effect; males are more likely to use alcohol to cope with chronic pain problems than females. Recently, a new conceptualization has emerged, proposing that the negative affective component of pain drives and maintains alcohol‐related behaviors. We studied in a longitudinal fashion alterations in alcohol drinking patterns and pain thresholds in a mouse model of chronic neuropathic pain in a sex‐dependent manner. Following partial denervation (spared nerve injury [SNI]), stimulus‐evoked pain responses were measured before chronic alcohol consumption, during drinking, during a deprivation phase, and following an episode of excessive drinking. During the course of alcohol drinking, we observed pronounced sex differences in pain thresholds. Male mice showed a strong increase in pain thresholds, suggesting an analgesic effect induced by alcohol over time, an effect that was not observed in female mice. SNI mice did not differ from sham‐operated controls in baseline alcohol consumption. However, following a deprivation phase and the reintroduction of ethanol, male SNI mice but not female mice showed more pronounced excessive drinking than controls. Finally, we observed decreased central ethanol sensitivity in male SNI mice but not in females. Together with our finding, that ethanol is able to decrease a pain‐induced negative affective memory we come to following conclusion. We propose that a lower sensitivity to the intoxicating effects of alcohol together with the ability of alcohol to reduce the negative affective component of pain may explain the higher co‐occurrence of AUD in male chronic pain patients.
机译:摘要慢性疼痛和酒精使用障碍(AUDS)的共同发生涉及遗传和神经生理方面之间的复杂相互作用,并且研究既有共同发生时则报告了混合发现。还有一种性别依赖效果的指示;男性更有可能使用酒精来应对慢性疼痛问题而不是女性。最近,已经出现了一种新的概念化,提出疼痛驱动的负面情感成分并保持与酗酒有关的行为。我们以依赖性方式在小鼠慢性神经病疼痛的小鼠模型中纵向时尚改变的纵向时尚改变和疼痛阈值。部分假期(腐烂神经损伤[SNI]),在饮用期间,在剥夺阶段,饮用期间,在剥夺阶段进行饮用期间,并在过度饮用中的一集中测量刺激诱发的疼痛反应。在酒精饮用过程中,我们观察到疼痛阈值的明显性别差异。雄性小鼠表现出疼痛阈值的强烈增加,表明酒精随时间诱导的镇痛作用,雌性小鼠未观察到的效果。 SNI小鼠没有与基线酒精消耗中的假手术控制不同。然而,在剥夺阶段和乙醇的重新制定后,雄性小鼠但不是雌性小鼠比对照表现出更明显的过度饮用。最后,我们观察到雄性SNI小鼠中的中央乙醇敏感性降低,但不在女性中。与我们的发现一起,乙醇能够减少痛苦引起的负面情感记忆,我们得出结论。我们提出对酒精令人令人稳定的敏感性与酒精减少疼痛的负面情感成分的能力较低,可以解释男性慢性疼痛患者的患者的较高共同发生。

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