Canonical Transient Receptor Potential (TRPC) Channels in Nociception and Pathological Pain.
Zhi-Chuan SunSui-Bin MaWen-Guang ChuDong JiaCeng LuoPublished in: Neural plasticity (2020)
Chronic pathological pain is one of the most intractable clinical problems faced by clinicians and can be devastating for patients. Despite much progress we have made in understanding chronic pain in the last decades, its underlying mechanisms remain elusive. It is assumed that abnormal increase of calcium levels in the cells is a key determinant in the transition from acute to chronic pain. Exploring molecular players mediating Ca2+ entry into cells and molecular mechanisms underlying activity-dependent changes in Ca2+ signaling in the somatosensory pain pathway is therefore helpful towards understanding the development of chronic, pathological pain. Canonical transient receptor potential (TRPC) channels form a subfamily of nonselective cation channels, which permit the permeability of Ca2+ and Na+ into the cells. Initiation of Ca2+ entry pathways by these channels triggers the development of many physiological and pathological functions. In this review, we will focus on the functional implication of TRPC channels in nociception with the elucidation of their role in the detection of external stimuli and nociceptive hypersensitivity.
Keyphrases
- chronic pain
- induced apoptosis
- pain management
- neuropathic pain
- cell cycle arrest
- end stage renal disease
- endoplasmic reticulum stress
- chronic kidney disease
- ejection fraction
- mental health
- newly diagnosed
- prognostic factors
- spinal cord injury
- vascular smooth muscle cells
- risk assessment
- cell death
- protein kinase
- single molecule
- cell proliferation
- spinal cord
- respiratory failure
- endothelial cells
- climate change
- human health
- patient reported outcomes
- brain injury
- binding protein
- label free