Department of Surgery, Miller School of Medicine, University of Miami, Miami, FL, USA.
Sci Prog. 2024 Jul-Sep;107(3):368504241264994. doi: 10.1177/00368504241264994.
Millions of people suffer from opioid use disorder, because of the ongoing opioid epidemic. The aversive symptoms of withdrawal are a leading factor for drug relapses, yet there are limited therapeutic options to minimize or prevent withdrawal symptoms. The mechanism behind opioid withdrawal is still not fully understood, thus preventing the development of new therapeutics. This study is an extension of our previously proposed mechanism of a toll-like receptor 2 (TLR2) mediated withdrawal response as a result of morphine induced microbial change that occurs during morphine withdrawal. Transcriptome analysis of the pre-frontal cortex indicated that there was increased expression of genes related to TLR2 signaling in morphine withdrawal treated animals compared to placebo controls. Antibiotic treatment further altered TLR2 related genes, recovering some of the morphine induced effect and leading to additional suppression of some genes related to the TLR2 pathway. Morphine withdrawal induced gene expression was attenuated in a whole body TLR2 knockout model. These results provide more support that TLR2 plays an integral role in morphine withdrawal mechanisms and could be a potential therapeutic target to minimize opioid withdrawal associated co-morbidities.
数以百万计的人患有阿片类药物使用障碍,这是由于阿片类药物的持续流行。戒断的不良反应是导致药物复发的主要因素,但减轻或预防戒断症状的治疗方法有限。阿片类药物戒断的机制尚不完全清楚,从而阻止了新疗法的开发。这项研究是我们之前提出的吗啡诱导微生物变化引起的 Toll 样受体 2 (TLR2) 介导的戒断反应机制的延伸,该机制发生在吗啡戒断期间。前额叶皮层的转录组分析表明,与安慰剂对照组相比,吗啡戒断处理的动物中与 TLR2 信号相关的基因表达增加。抗生素治疗进一步改变了 TLR2 相关基因,恢复了一些吗啡诱导的效应,并导致一些与 TLR2 途径相关的基因受到额外抑制。全身 TLR2 基因敲除模型中,吗啡戒断诱导的基因表达减弱。这些结果进一步支持 TLR2 在吗啡戒断机制中发挥重要作用,并可能成为减轻阿片类药物戒断相关共病的潜在治疗靶点。