Yi Shuyuan, Cao Hong, Zheng Weilei, Wang Yin, Li Peifeng, Wang Shoushi, Zhou Zhixia
Institute for Translational Medicine, The Affiliated Hospital of Qingdao University, College of Medicine, Qingdao University, Qingdao 266021, China; Department of Anaesthesiology, Affiliated Qingdao Central Hospital of Qingdao University, Qingdao Cancer Hospital, Qingdao 266042, China; School of Anesthesiology, Weifang Medical University, Weifang 261053, China.
Department of Anaesthesiology, Affiliated Qingdao Central Hospital of Qingdao University, Qingdao Cancer Hospital, Qingdao 266042, China.
Biomed Pharmacother. 2023 Nov;167:115472. doi: 10.1016/j.biopha.2023.115472. Epub 2023 Sep 15.
Opioids are widely used in clinical practice by activating opioid receptors (OPRs), but their clinical application is limited by a series of side effects. Researchers have been making tremendous efforts to promote the development and application of opioids. Fortunately, recent studies have identified the additional effects of opioids in addition to anesthesia and analgesia, particularly in terms of organ protection against ischemia-reperfusion (I/R) injury, with unique advantages. I/R injury in vital organs not only leads to cell dysfunction and structural damage but also induces acute and chronic organ failure, even death. Early prevention and appropriate therapeutic targets for I/R injury are crucial for organ protection. Opioids have shown cardioprotective effects for over 20 years, especially remifentanil, a derivative of fentanyl, which is a new ultra-short-acting opioid analgesic widely used in clinical anesthesia induction and maintenance. In this review, we provide current knowledge about the physiological effects related to OPR-mediated organ protection, focusing on the protective effect and mechanism of remifentanil on I/R injury in the heart and other vital organs. Herein, we also explored the potential application of remifentanil in clinical I/R injury. These findings provide a theoretical basis for the use of remifentanil to inhibit or alleviate organ I/R injury during the perioperative period and provide insights for opioid-induced human organ protection and drug development.
阿片类药物通过激活阿片受体(OPRs)在临床实践中广泛应用,但其临床应用受到一系列副作用的限制。研究人员一直在努力推动阿片类药物的开发和应用。幸运的是,最近的研究发现了阿片类药物除麻醉和镇痛作用外的其他作用,特别是在对器官缺血再灌注(I/R)损伤的保护方面,具有独特优势。重要器官的I/R损伤不仅会导致细胞功能障碍和结构损伤,还会引发急性和慢性器官衰竭,甚至死亡。I/R损伤的早期预防和合适的治疗靶点对于器官保护至关重要。二十多年来,阿片类药物已显示出心脏保护作用,尤其是瑞芬太尼,它是芬太尼的衍生物,是一种新型超短效阿片类镇痛药,广泛用于临床麻醉诱导和维持。在本综述中,我们提供了有关OPR介导的器官保护相关生理效应的现有知识,重点关注瑞芬太尼对心脏和其他重要器官I/R损伤的保护作用及机制。在此,我们还探讨了瑞芬太尼在临床I/R损伤中的潜在应用。这些发现为围手术期使用瑞芬太尼抑制或减轻器官I/R损伤提供了理论依据,并为阿片类药物诱导的人体器官保护和药物开发提供了见解。