TRPV1-FAAH-COX: The Couples Game in Pain Treatment

被引:23
作者
Aiello, Francesca [2 ]
Carullo, Gabriele [2 ]
Badolato, Mariateresa [2 ]
Brizzi, Antonella [1 ]
机构
[1] Univ Siena, Dipartimento Biotecnol Chim & Farm, Polo Sci S Miniato, I-53100 Siena, Italy
[2] Univ Calabria, Dipartimento Farm & Sci Salute & Nutr, Edificio Polifunz, I-87036 Arcavacata Di Rende, Italy
关键词
drug discovery; dual inhibitors; enzymes; pain treatment; receptors; ACID AMIDE HYDROLASE; REDUCES NEUROPATHIC PAIN; VANILLOID RECEPTOR TRPV1; CANNABINOID RECEPTORS; INHIBITOR URB597; RAT MODEL; CYCLOOXYGENASE; FAAH; MECHANISM; ANALGESIA;
D O I
10.1002/cmdc.201600111
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
Pain is a complex sensation involving the perception and transduction of diverse environmental pain stimuli with cognitive and emotional processing by the central nervous system. It can manifest as acute or chronic pain. Pain is controlled by a series of enzymes and receptors, implicated in a variety of interconnected mechanisms and pathways. In fact, several studies have shown the cannabinoid receptor1 and the transient receptor potential vanilloid channel1 to be new players in modulating the sophisticated pain transduction system at the central level. At the peripheral level, the perception of pain involves cyclooxygenases and fatty acid amide hydrolase, as recent studies demonstrate. This Minireview describes the physiological aspects of the receptors and enzymes mentioned above and focuses on the consideration of dual mechanisms as a new therapeutic approach in the treatment of pain.
引用
收藏
页码:1686 / 1694
页数:9
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