Maija Haanpää, Rolf-Detlef Treede
Department of Neurosurgery, Helsinki University Central Hospital, Töölö Hospital, Helsinki, Finland.
European neurology 2012Capsaicin has long been used as a traditional medicine to treat pain and, recently, its mechanism of analgesic action has been discovered. This review article documents the clinical development of capsaicin to demonstrate that pharmacognosy still has a profound influence on modern-day drug development programs. Capsaicin is a highly selective agonist for the transient receptor potential channel vanilloid-receptor type 1 (TRPV1), which is expressed on central and peripheral terminals of nociceptive primary sensory neurons. Knockout studies have revealed the importance of TRPV1 as a molecular pain integrator and target for novel analgesic agents. Topical application of capsaicin at the peripheral terminal of TRPV1-expressing neurons superficially denervates the epidermis in humans in a highly selective manner and results in hypoalgesia. In three recent randomized controlled trials, a patch containing high-concentration capsaicin demonstrated meaningful efficacy and tolerability relative to a low-concentration capsaicin control patch in patients with peripheral neuropathic pain. Data from clinical practice will determine if the high-concentration capsaicin patch is effective in real-world settings. Copyright © 2012 S. Karger AG, Basel.
Maija Haanpää, Rolf-Detlef Treede. Capsaicin for neuropathic pain: linking traditional medicine and molecular biology. European neurology. 2012;68(5):264-75
PMID: 23037991
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