Advances in the Treatment of Chronic Pain by Targeting GPCRs

被引:13
作者
Che, Tao [1 ,2 ,3 ]
机构
[1] Washington Univ, Sch Med, Dept Anesthesiol, St Louis, MO 63110 USA
[2] St Louis Coll Pharmacol, Ctr Clin Pharmacol, St Louis, MO 63110 USA
[3] Washington Univ, St Louis, MO 63110 USA
关键词
DELTA-OPIOID RECEPTOR; PROTEIN-COUPLED RECEPTOR; DORSAL-ROOT GANGLIA; NEUROPATHIC PAIN; BETA-ARRESTIN; GLUTAMATE RECEPTORS; CRYSTAL-STRUCTURE; INTRAMUSCULAR INJECTION; CANNABINOID RECEPTORS; MOLECULAR-MECHANISMS;
D O I
10.1021/acs.biochem.0c00644
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pain is an essential protective mechanism that the body uses to alert or prevent further damage. Pain sensation is a complex event involving perception, transmission, processing, and response. Neurons at different levels (peripheral, spinal cord, and brain) are responsible for these pro- or antinociceptive activities to ensure an appropriate response to external stimuli. The terminals of these neurons, both in the peripheral endings and in the synapses, are equipped with G protein-coupled receptors (GPCRs), voltage- and ligand-gated ion channels that sense structurally diverse stimuli and inhibitors of neuronal activity. This review will focus on the largest class of sensory proteins, the GPCRs, as they are distributed throughout ascending and descending neurons and regulate activity at each step during pain transmission. GPCR activation also directly or indirectly controls the function of co-localized ion channels. The levels and types of some GPCRs are significantly altered in different pain models, especially chronic pain states, emphasizing that these molecules could be new targets for therapeutic intervention in chronic pain.
引用
收藏
页码:1401 / 1412
页数:12
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