Abstract
Endogenous palmitoylethanolamide (PEA) has a key role in pain modulation. Central or peripheral PEA can reduce nociceptive behavior, but no study has yet reported a descending inhibitory effect on the neuronal nociceptive activity of Aδ- and C-fibers. This study shows that intracisternal PEA inhibits the peripheral nociceptive responses of dorsal horn wide dynamic range cells (i.e., inhibition of Aδ- and C-fibers), an effect blocked by spinal methiothepin. These results suggest that a descending analgesic mechanism mediated by the serotonergic system could be activated by central PEA.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Action Potentials / drug effects*
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Amides
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Analgesics / pharmacology*
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Animals
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Electric Stimulation
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Ethanolamines / pharmacology*
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Laminectomy
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Male
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Methiothepin / pharmacology
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Nerve Fibers, Myelinated / drug effects
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Nerve Fibers, Myelinated / physiology
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Nociceptors / drug effects*
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Palmitic Acids / pharmacology*
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Patch-Clamp Techniques
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Rats
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Rats, Wistar
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Serotonin Antagonists / pharmacology
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Spinal Cord Dorsal Horn / cytology*
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Subarachnoid Space / drug effects
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Subarachnoid Space / physiology
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Time Factors
Substances
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Amides
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Analgesics
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Ethanolamines
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Palmitic Acids
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Serotonin Antagonists
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Methiothepin
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palmidrol