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Phospholipase C{beta}3 in mouse and human dorsal root ganglia and spinal cord is a possible target for treatment of neuropathic pain

Shi, TJS (author)
Karolinska Institutet
Liu, SXL (author)
Hammarberg, H (author)
Karolinska Institutet
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Watanabe, M (author)
Xu, ZQD (author)
Karolinska Institutet
Hokfelt, T (author)
Karolinska Institutet
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 (creator_code:org_t)
2008-12-16
2008
English.
In: Proceedings of the National Academy of Sciences of the United States of America. - : Proceedings of the National Academy of Sciences. - 1091-6490. ; 105:50, s. 20004-20008
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Treatment of neuropathic pain is a major clinical problem. This study shows expression of phospholipase ß3 (PLCß3) in mouse and human DRG neurons, mainly in small ones and mostly with a nonpeptidergic phenotype. After spared nerve injury, the pain threshold was strongly reduced, and systemic treatment of such animals with the unselective PLC inhibitor U73122 caused a rapid and long-lasting (48-h) increase in pain threshold. Thus, inhibition of PLC may provide a way to treat neuropathic pain.

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