Ion channels involved in inflammation and pain in osteoarthritis and related musculoskeletal disorders

被引:10
作者
Matta, Csaba [1 ]
Takacs, Roland [1 ]
Ducza, Laszlo [1 ]
Ebeid, Rana Abdelsattar [1 ]
Choi, Heonsik [2 ]
Mobasheri, Ali [3 ,4 ,5 ,6 ,7 ,8 ]
机构
[1] Univ Debrecen, Fac Med, Dept Anat Histol & Embryol, Debrecen, Hungary
[2] Kolon Ind Inc, Healthcare Res Inst, Kolon Adv Res Ctr, Seoul, South Korea
[3] Univ Oulu, Fac Med, Res Unit Med Imaging Phys & Technol, Oulu, Finland
[4] State Res Inst Ctr Innovat Med, Dept Regenerat Med, Vilnius, Lithuania
[5] Univ Med Ctr Utrecht, Dept Orthoped, Utrecht, Netherlands
[6] Univ Med Ctr Utrecht, Dept Rheumatol & Clin Immunol, Utrecht, Netherlands
[7] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Joint Surg, Guangzhou, Guangdong, Peoples R China
[8] Univ Liege, World Hlth Org Collaborating Ctr Publ Hlth Aspects, Liege, Belgium
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2023年 / 325卷 / 01期
基金
芬兰科学院;
关键词
analgesics; channelome; ion channels; nociception; osteoarthritis; HYDROGEN-SULFIDE; GLUTAMATE RECEPTORS; THERAPEUTIC TARGETS; KNEE OSTEOARTHRITIS; POTASSIUM CHANNELS; GANGLION NEURONS; PERIPHERAL PAIN; SKELETAL-MUSCLE; SYNOVIAL-FLUID; POTENTIAL ROLE;
D O I
10.1152/ajpcell.00040.2023
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Osteoarthritis (OA) is a currently incurable, chronic, progressive, and debilitating musculoskeletal (MSK) condition. One of its hall -mark symptoms is chronic nociceptive and neuropathic pain, which significantly reduces the quality of life of patients with OA. Although research into the pathomechanisms of OA pain is ongoing and several pain pathways are well understood, the true source of OA pain remains unclear. Ion channels and transporters are key mediators of nociceptive pain. In this narrative review article, we summarize the state-of-the-art in relation to the distribution and function of ion channels in all major synovial joint tis-sues in the context of pain generation. We provide an update on the ion channels likely involved in mediating peripheral and central nociceptive pathways in the nervous system in OA pain, including voltage-gated sodium and potassium channels, mem-bers of the transient receptor potential (TRP) channel family, and purinergic receptor complexes. We focus on ion channels and transporters that have the potential to be candidate drug targets for pain management in patients with OA. We propose that ion channels expressed by the cells of constituent tissues of OA-afflicted synovial joints including cartilage, bone, synovium, liga-ment, and muscle, should be more thoroughly investigated and targeted in the context of OA pain. Based on key findings from recent basic research articles as well as clinical trials, we propose novel directions for the development of future analgesic thera-pies to improve the quality of life of patients with OA.
引用
收藏
页码:C257 / C271
页数:15
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