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Targeting Pain-evoking Transient Receptor Potential Channels for the Treatment of Pain

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Date 2014 Jan 8
PMID 24396340
Citations 11
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Abstract

Chronic pain affects billions of lives globally and is a major public health problem in the United States. However, pain management is still a challenging task due to a lack of understanding of the fundamental mechanisms of pain. In the past decades transient receptor potential (TRP) channels have been identified as molecular sensors of tissue damage and inflammation. Activation/sensitization of TRP channels in peripheral nociceptors produces neurogenic inflammation and contributes to both somatic and visceral pain. Pharmacological and genetic studies have affirmed the role of TRP channels in multiple forms of inflammatory and neuropathic pain. Thus pain-evoking TRP channels emerge as promising therapeutic targets for a wide variety of pain and inflammatory conditions.

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References
1.
Xu G, Winston J, Shenoy M, Yin H, Pendyala S, Pasricha P . Transient receptor potential vanilloid 1 mediates hyperalgesia and is up-regulated in rats with chronic pancreatitis. Gastroenterology. 2007; 133(4):1282-92. DOI: 10.1053/j.gastro.2007.06.015. View

2.
Gavva N, Treanor J, Garami A, Fang L, Surapaneni S, Akrami A . Pharmacological blockade of the vanilloid receptor TRPV1 elicits marked hyperthermia in humans. Pain. 2008; 136(1-2):202-10. DOI: 10.1016/j.pain.2008.01.024. View

3.
Puopolo M, Binshtok A, Yao G, Oh S, Woolf C, Bean B . Permeation and block of TRPV1 channels by the cationic lidocaine derivative QX-314. J Neurophysiol. 2013; 109(7):1704-12. PMC: 3628012. DOI: 10.1152/jn.00012.2013. View

4.
Jaggi A, Singh N . Therapeutic targets for the management of peripheral nerve injury-induced neuropathic pain. CNS Neurol Disord Drug Targets. 2011; 10(5):589-609. DOI: 10.2174/187152711796235041. View

5.
Bautista D, Jordt S, Nikai T, Tsuruda P, Read A, Poblete J . TRPA1 mediates the inflammatory actions of environmental irritants and proalgesic agents. Cell. 2006; 124(6):1269-82. DOI: 10.1016/j.cell.2006.02.023. View