Peptide Inhibitor of Morphine- and β -Endorphin-Induced Analgesia

The synthetic β -endorphin analogs with the omission of the NH2-terminal [Met]enkephalin segment [β -endorphin-(6-31) and β -endorphin-(20-31)] are shown to inhibit morphine- or β -endorphin-induced analgesia in mice by the tail-flick test, whereas the synthetic NH2-terminal pentadecapeptide β -endo...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 1980-09, Vol.77 (9), p.5525-5526
Hauptverfasser: Lee, Nancy M., Friedman, Howard J., Leybin, Leonid, Cho, Tae Mook, Loh, Horace H., Li, Choh Hao
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Sprache:eng
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Zusammenfassung:The synthetic β -endorphin analogs with the omission of the NH2-terminal [Met]enkephalin segment [β -endorphin-(6-31) and β -endorphin-(20-31)] are shown to inhibit morphine- or β -endorphin-induced analgesia in mice by the tail-flick test, whereas the synthetic NH2-terminal pentadecapeptide β -endorphin-(1-15) has no inhibitory activity. This study raises the possibility that endogenous inhibiting peptides exist in the brain which play a role in the regulation of endorphin actions.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.77.9.5525