Institut de Chimie Moléculaire de Reims, UMR 7312-CNRS, UFR Pharmacie , Université de Reims Champagne-Ardenne , 51 rue Cognacq-Jay , 51096 Reims Cedex , France.
Structure Fédérative de Recherche-Champagne Ardenne Picardie Santé (SFR-CAP Santé) , 51095 Reims Cedex , France.
J Med Chem. 2018 Mar 8;61(5):1745-1766. doi: 10.1021/acs.jmedchem.7b00115. Epub 2017 Aug 22.
Alcohol use disorder (AUD) represents a serious public health issue, and discovery of new therapies is a pressing necessity. Alcohol exposure has been widely demonstrated to modulate epigenetic mechanisms, such as histone acetylation/deacetylation balance, in part via histone deacetylase (HDAC) inhibition. Epigenetic factors have been suggested to play a key role in AUD. To date, 18 different mammalian HDAC isoforms have been identified, and these have been divided into four classes. Since recent studies have suggested that both epigenetic mechanisms underlying AUD and the efficacy of HDAC inhibitors (HDACIs) in different animal models of AUD may involve class I HDACs, we herein report the development of class I HDACIs, including information regarding their structure, potency, and selectivity. More effort is required to improve the selectivity, pharmacokinetics, and toxicity profiles of HDACIs to achieve a better understanding of their efficacy in reducing addictive behavior.
酒精使用障碍(AUD)是一个严重的公共卫生问题,发现新的治疗方法迫在眉睫。广泛的研究表明,酒精暴露会调节表观遗传机制,如组蛋白乙酰化/去乙酰化平衡,部分通过组蛋白去乙酰化酶(HDAC)抑制。表观遗传因素被认为在 AUD 中发挥关键作用。迄今为止,已经鉴定出 18 种不同的哺乳动物 HDAC 同工酶,并将其分为四类。由于最近的研究表明,AUD 的表观遗传机制以及不同 AUD 动物模型中 HDAC 抑制剂(HDACIs)的疗效可能涉及 I 类 HDAC,因此我们在此报告 I 类 HDACIs 的开发情况,包括它们的结构、效力和选择性的信息。需要进一步努力提高 HDACIs 的选择性、药代动力学和毒性特征,以更好地了解它们在减少成瘾行为方面的疗效。