| Literature DB >> 30042091 |
Ya-Qun Zhou1, Dai-Qiang Liu1, Shu-Ping Chen1, Jia Sun1, Xiao-Mei Wang1, Yu-Ke Tian1, Wei Wu2, Da-Wei Ye3.
Abstract
Chronic pain remains to be a clinical challenge due to insufficient therapeutic strategies. Minocycline is a member of the tetracycline class of antibiotics, which has been used in clinic for decades. It is frequently reported that minocycline may has many non-antibiotic properties, among which is its anti-nociceptive effect. The results from our lab and others suggest that minocycline exerts strong analgesic effect in animal models of chronic pain including visceral pain, chemotherapy-induced periphery neuropathy, periphery injury induced neuropathic pain, diabetic neuropathic pain, spinal cord injury, inflammatory pain and bone cancer pain. In this review, we summarize the mechanisms underlying the analgesic effect of minocycline in preclinical studies. Due to a good safety record when used chronically, minocycline may become a promising therapeutic strategy for chronic pain in clinic.Entities:
Keywords: Arabinofuranosyl cytidine (PubChem CID: 6253); Astrocyte; Bee venom (PubChem CID: 133082063); Capsaicin (PubChem CID: 1548943); Carrageenan (PubChem CID: 6850766); Chronic pain; Cytokines; Microglia; Minocycline; Minocycline (PubChem CID: 54675783); Paclitaxel (PubChem CID: 36314); SB203580 (PubChem CID: 176155); Vincristine (PubChem CID: 5978)
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Year: 2018 PMID: 30042091 DOI: 10.1016/j.phrs.2018.07.002
Source DB: PubMed Journal: Pharmacol Res ISSN: 1043-6618 Impact factor: 7.658