A Genetically Modified Skin Graft for Treating Alcohol Use Disorder and/or Polysubstance Abuse With Cocaine.

Advances in drug and alcohol research Pub Date : 2021-06-18 eCollection Date: 2021-01-01 DOI:10.3389/adar.2021.10007
Qingyao Kong, Xiaoyang Wu, Ming Xu
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Abstract

Alcohol use disorder (AUD) is one of the foremost public health problems. Alcohol is also frequently co-abused with cocaine. There is a huge unmet need for the treatment of AUD and/or cocaine co-abuse. We have developed and used a skin stem cell-based gene delivery platform and found that production of the glucagon-like peptide-1 (GLP1) from the grafted genetically modified skin reduced development and reinstatement of alcohol-induced drug-taking and seeking, voluntary oral alcohol consumption and alcohol-induced increase in dopamine (DA) levels in the nucleus accumbens (NAc). Moreover, we have developed a novel co-grafting procedure for both modified human butyrylcholinesterase (hBChE)- and GLP1-expressing cells. Skin grafts-derived hBChE and GLP1 reduced acquisition of drug-taking and toxicity induced by concurrent alcohol and cocaine injections. These results imply that gene delivery through skin transplants may add a new option to treat drug abuse and co-abuse.

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一种用于治疗可卡因酒精使用障碍和/或多物质滥用的转基因皮肤移植物
酒精使用障碍(AUD)是最重要的公共卫生问题之一。酒精也经常与可卡因一起被滥用。对澳元和/或可卡因共同滥用的治疗存在巨大的未满足需求。我们开发并使用了一种基于皮肤干细胞的基因传递平台,发现从移植的转基因皮肤中产生胰高血糖素样肽-1 (GLP1)减少了酒精诱导的药物摄入和寻求的发展和恢复,自愿口服酒精摄入和酒精诱导的伏隔核(NAc)多巴胺(DA)水平的增加。此外,我们已经开发了一种新的共嫁接方法,用于修饰的人丁基胆碱酯酶(hBChE)-和表达glp1的细胞。皮肤移植物衍生的hBChE和GLP1减少了酒精和可卡因同时注射引起的药物摄取和毒性。这些结果表明,通过皮肤移植的基因传递可能为治疗药物滥用和共同滥用提供了一种新的选择。
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