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- W2080498739 abstract "Neurogenic inflammation and ensuing pain can be modulated by inhibiting the function of primary afferent neurons. The best studied mechanism to accomplish such inhibition is the opioid system. Under inflammatory conditions, the anterograde axonal transport of opioid receptors from dorsal root ganglia toward the peripheral sensory nerve endings is augmented. The increased number of opioid receptors (among other mechanisms) leads to improved analgesic effects of exogenously administered ligands (eg, morphine) and of endogenous leukocyte-derived opioid peptides (eg, beta-endorphin). A current concept proposes that during inflammatory processes endogenous opioid peptides can be secreted from immunocytes, occupy peripheral opioid receptors on sensory nerve endings, and produce analgesia by inhibiting the excitability of these nerves or the release of proinflammatory neuropeptides. This article focuses on the role of peripheral opioid receptors in pain control and on novel pharmaceutical concepts for the treatment of patients who suffer from rheumatoid arthritis and other inflammatory pain." @default.
- W2080498739 created "2016-06-24" @default.
- W2080498739 creator A5024748471 @default.
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- W2080498739 date "2005-02-01" @default.
- W2080498739 modified "2023-10-11" @default.
- W2080498739 title "Controlling Pain by Influencing Neurogenic Pathways" @default.
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- W2080498739 doi "https://doi.org/10.1016/j.rdc.2004.09.001" @default.
- W2080498739 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/15639058" @default.
- W2080498739 hasPublicationYear "2005" @default.
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