Research progress regarding endocannabinoid system involvement in pain modulation and electroacupuncture analgesia

被引:0
|
作者
Qin, Renjie [1 ]
Wu, Yisong [1 ]
Jin, Nuo [1 ]
Xu, Xingzhi [1 ]
Lan, Yuye [1 ]
Jing, Xianghong [2 ]
Li, Man [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Sch Basic Med, Key Lab Anesthesiol & Resuscitat,Minist Educ, Wuhan, Peoples R China
[2] China Acad Chinese Med Sci, Inst Acupuncture & Moxibust, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
Electroacupuncture; Endocannabinoid receptors; Inflammatory pain; Neuropathic pain; BONE CANCER PAIN; CANNABINOID RECEPTOR; INFLAMMATORY PAIN; SPINAL-CORD; MURINE MODEL; CB1; RECEPTOR; ACTIVATION; MECHANISMS; EXPRESSION; PHARMACOLOGY;
D O I
10.1097/HM9.0000000000000142
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Pain is a subjective and unpleasant sensation that significantly impacts the daily lives of individuals. Chronic pain represents one of the most challenging public health issues, and ensuring effective pain management is a fundamental right of individuals and a sacred duty of healthcare providers. Cannabis, one of the earliest recognized medicinal plants, contains cannabinoids, which are non-opioid substances that modulate nociceptive responses. Electroacupuncture (EA), characterized by its low-risk and well-tolerated nature, is pivotal in pain management. The endocannabinoid system consists of endocannabinoids, cannabinoid receptors, and enzymes involved in endocannabinoid synthesis, degradation, and transport. Recently, the role of the endocannabinoid system in pain development and EA analgesia has attracted considerable research attention. Studies have highlighted the role of the endocannabinoid system in various types of pain, including inflammatory pain, neuropathic pain, and cancer-related pain, as well as in EA analgesia. This study aims to review the mechanisms of endocannabinoid system involvement in pain modulation and EA analgesia to provide insights to inform clinical approaches to pain management.
引用
收藏
页码:36 / 45
页数:10
相关论文
empty
未找到相关数据