Department of Physiology and Comprehensive Alcohol-HIV/AIDS Research Center, LSU Health Sciences Center, New Orleans, LA, 70112, USA.
Department of Physiology and Comprehensive Alcohol-HIV/AIDS Research Center, LSU Health Sciences Center, New Orleans, LA, 70112, USA.
Neuropharmacology. 2020 Sep 1;174:108153. doi: 10.1016/j.neuropharm.2020.108153. Epub 2020 May 26.
Substance use disorders (SUDs) are frequently accompanied by affective symptoms that promote negative reinforcement mechanisms contributing to SUD maintenance or progression. Despite their widespread use as analgesics, chronic or excessive exposure to alcohol, opioids, and nicotine produces heightened nociceptive sensitivity, termed hyperalgesia. This review focuses on the contributions of neuropeptide (CRF, melanocortin, opioid peptide) and cytokine (IL-1β, TNF-α, chemokine) systems in the development and maintenance of substance-induced hyperalgesia. Few effective therapies exist for either chronic pain or SUD, and the common interaction of these disease states likely complicates their effective treatment. Here we highlight promising new discoveries as well as identify gaps in research that could lead to more effective and even simultaneous treatment of SUDs and co-morbid hyperalgesia symptoms.
物质使用障碍(SUD)通常伴随着情感症状,这些症状促进了负强化机制,从而导致 SUD 的维持或进展。尽管它们被广泛用作镇痛药,但长期或过量接触酒精、阿片类药物和尼古丁会导致痛觉敏感性增加,称为痛觉过敏。本综述重点介绍了神经肽(CRF、黑色素皮质素、阿片肽)和细胞因子(IL-1β、TNF-α、趋化因子)系统在物质诱导的痛觉过敏发展和维持中的作用。目前,针对慢性疼痛或 SUD 的有效治疗方法很少,而这些疾病状态的常见相互作用可能使它们的有效治疗变得更加复杂。在这里,我们强调了有前途的新发现,并确定了研究中的差距,这些差距可能会导致更有效甚至同时治疗 SUD 和共病性痛觉过敏症状。