The potential remedy of melatonin on osteoarthritis.
Ko-Hsiu LuPeace Wun-Ang LuEric Wun-Hao LuChih-Hsin TangShih-Chi SuChiao-Wen LinChiao-Wen LinPublished in: Journal of pineal research (2021)
Osteoarthritis (OA), the most common arthritis worldwide, is a degenerative joint disease characterized by progressive cartilage breakdown, subchondral remodeling, and synovial inflammation. Although conventional pharmaceutical therapies aimed to prevent further cartilage loss and joint dysfunction, there are no ideal strategies that target the pathogenesis of OA. Melatonin exhibits a variety of regulatory properties by binding to specific receptors and downstream molecules and exerts a myriad of receptor-independent actions via intracellular targets as a chondrocyte protector, an anti-inflammation modulator, and a free radical scavenger. Melatonin also modulates cartilage regeneration and degradation by directly/indirectly regulating the expression of main circadian clock genes, such as transcriptional activators [brain and muscle aryl hydrocarbon receptor nuclear translocator-like protein (Bmal) and circadian locomotor output cycles kaput (Clock)], transcriptional repressors [period circadian regulator (Per)1/2, cryptochrome (Cry)1/2, and Dec2], and nuclear hormone receptors [Rev-Erbs and retinoid acid-related orphan receptors (Rors)]. Owing to its effects on cartilage homeostasis, we propose a potential role for melatonin in the prevention and therapy of OA via the modulation of circadian clock genes, mitigation of chondrocyte apoptosis, anti-inflammatory activity, and scavenging of free radicals.
Keyphrases
- oxidative stress
- knee osteoarthritis
- transcription factor
- extracellular matrix
- rheumatoid arthritis
- genome wide
- gene expression
- poor prognosis
- stem cells
- binding protein
- multiple sclerosis
- genome wide identification
- spinal cord injury
- climate change
- endoplasmic reticulum stress
- bioinformatics analysis
- white matter
- risk assessment
- dna methylation
- cell death
- brain injury
- signaling pathway
- blood brain barrier
- mesenchymal stem cells
- bone marrow
- genome wide analysis