Fornasari Diego, Cuomo Arturo
Department of Medical Biotechnology and Translational Medicine, Università degli Studi di Milano, Milan, Italy.
Department of Anesthesia and Critical Care, Istituto Nazionale Tumori IRCCS Fondazione Pascale, Naples, Italy.
Pain Ther. 2025 Jun 22. doi: 10.1007/s40122-025-00753-3.
Buprenorphine has gained significant attention for its unique pharmacological properties, making it a valuable tool in chronic pain management. Unlike traditional opioids, buprenorphine's partial and biased agonist actions at the μ-opioid receptor provide potent analgesia while minimizing risks such as respiratory depression, tolerance, and dependence. Its favorable pharmacokinetic profile provides the potential for expanding its clinical use in different patient populations. A literature search was conducted in PubMed, Web of Science, and Google Scholar to identify peer-reviewed studies on recent developments in the pharmacological features and new clinical applications of buprenorphine, including original research, reviews, and consensus statements. This comprehensive review explores the expanding clinical applications of buprenorphine, emphasizing its role in managing chronic pain in elderly patients, individuals with cardiac conditions, and those with renal impairments. Emerging evidence highlights its utility in addressing chronic pain in younger adults and its potential in mitigating side effects associated with aromatase inhibitor therapy in patients with breast cancer. Additionally, buprenorphine's lower endocrine side-effect profile and antidepressant properties open new therapeutic avenues for pain-associated depression. With its unique pharmacodynamics, transdermal formulations for sustained drug release, and reduced adverse effects, buprenorphine represents a promising option for tailored, multimodal pain management strategies, especially in populations with complex medical needs. Further studies are warranted to confirm its broad therapeutic potential.
丁丙诺啡因其独特的药理特性而备受关注,使其成为慢性疼痛管理中的一种有价值的工具。与传统阿片类药物不同,丁丙诺啡对μ-阿片受体的部分激动和偏向激动作用可提供强效镇痛,同时将呼吸抑制、耐受性和依赖性等风险降至最低。其良好的药代动力学特征为扩大其在不同患者群体中的临床应用提供了潜力。在PubMed、科学网和谷歌学术上进行了文献检索,以确定关于丁丙诺啡药理特性最新进展和新临床应用的同行评审研究,包括原始研究、综述和共识声明。这篇综述探讨了丁丙诺啡不断扩大的临床应用,强调了其在管理老年患者、心脏病患者和肾功能损害患者慢性疼痛方面的作用。新出现的证据突出了其在解决年轻成年人慢性疼痛方面的效用,以及在减轻乳腺癌患者芳香化酶抑制剂治疗相关副作用方面的潜力。此外,丁丙诺啡较低的内分泌副作用特征和抗抑郁特性为疼痛相关性抑郁症开辟了新的治疗途径。凭借其独特的药效学、用于持续药物释放的透皮制剂以及减少的不良反应,丁丙诺啡是定制化多模式疼痛管理策略的一个有前景的选择,尤其是在有复杂医疗需求的人群中。有必要进行进一步研究以证实其广泛的治疗潜力。