Department of Physiology, Neuroscience Program, Michigan State University, East Lansing, Michigan 48824, USA.
Cold Spring Harb Perspect Med. 2021 Feb 1;11(2):a039362. doi: 10.1101/cshperspect.a039362.
Opioid drugs are highly valued as potent analgesics; however, there are significant risks associated with long-term use because of their abuse liability. Opioids cause changes in ventral tegmental area (VTA) gene expression and cell activity that have been linked to addiction-related behaviors in rodent models. Here, we focus on VTA dopamine (DA) neurons and review the cellular, structural, and synaptic plasticity changes induced by acute and chronic opioid exposure. We also discuss many avenues for future research including determination of whether opioid neuroadaptations are specific for subpopulations of VTA DA neurons. A better understanding of the molecular adaptations within the cells and circuits that drive opioid abuse is crucial for the development of better treatments for substance use disorders and to create novel, safer pain-relieving therapeutics.
阿片类药物作为强效镇痛药而备受重视;然而,由于其滥用倾向,长期使用存在显著风险。阿片类药物会引起腹侧被盖区 (VTA) 基因表达和细胞活性的变化,这些变化与啮齿类动物模型中的成瘾相关行为有关。在这里,我们专注于 VTA 多巴胺 (DA) 神经元,并综述了急性和慢性阿片类药物暴露所诱导的细胞、结构和突触可塑性变化。我们还讨论了许多未来的研究途径,包括确定阿片类药物神经适应性是否特定于 VTA DA 神经元的亚群。更好地了解驱动阿片类药物滥用的细胞和回路中的分子适应性,对于开发更好的物质使用障碍治疗方法以及创造新型、更安全的止痛治疗方法至关重要。