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Environmental stressors and alcoholism development: Focus on molecular targets and their epigenetic regulation

机译:环境压力源和酗酒发展:专注于分子靶点及其表观遗传调控

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摘要

Alcohol exposure and stressful events in life can induce long-lasting changes in physiology, behavior and gene expression patterns, eventually facilitating the development of psychiatric diseases like alcohol use disorders (AUD). Epigenetic mechanisms have been recently proposed to play a role in the cellular actions of alcohol via chromatin remodeling. Here we discuss interactions between stress and the pharmacological effects of alcohol, including the possibility that early exposure to, or withdrawal of, alcohol might induce stressful effects of their own. A specific aim is to describe novel molecular mechanisms by which stress, alcohol or their combined presentation impact on the epigenome. A key question is why only a fraction of the population progresses from regular, non-problematic, alcohol use to AUD, despite suffering from similar alcohol exposure. It is important to analyze how environmental factors, most notably stress, interact with the epigenetic machinery to increase vulnerability for AUD. The knowledge derived from this endeavor will be critical for the development of preventive strategies and new, drug- or gene-based, therapies.
机译:酒精暴露和生命中的压力事件可以诱导生理学,行为和基因表达模式的长期变化,最终促进饮酒障碍等精神疾病的发展(AUD)。最近已经提出了表观遗传机制在通过染色质重塑的醇细胞作用中发挥作用。在这里,我们讨论压力与酒精的药理作用之间的相互作用,包括早期暴露或戒断的可能性可能会引起自己的压力影响。特定目的是描述一种新的分子机制,通过这种分子机制,压力,酒精或其对外形组的影响。尽管患有类似的酒精曝光,但只有一小部分人口才能从常规,非问题,酒精用途中进展到澳元,为什么患有类似的酒精曝光。重要的是要分析环境因素如何,最符合的压力,与表观遗传机制互动以增加澳元的脆弱性。源于这一努力的知识对于制定预防策略和新的药物或基因,疗法至关重要。

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