Proceedings of the National Academy of Sciences of the United States of America, 76(12), 6666-6670, 1979

Dynorphin-(1-13), an extraordinarily potent opioid peptide

Michael W. Hunkapiller , Andrew Goldstein , L Hood

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  • Stanford University ROR
DOI10.1073/pnas.76.12.6666 PMID230519
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Abstract

We describe the opioid properties of a tridecapeptide, the sequence of which corresponds to the NH2-terminal sequence of dynorphin, a novel porcine pituitary endorphin. It contains [Leu]enkephalin. In the guinea pig ileum longitudinal muscle preparation it is about 700 times more potent than [Leu]enkephalin. Its effects in this tissue are blocked completely by naloxone, but the apparent affinity of naloxone is 1/13th that for blockade of [Leu]enkephalin or normorphine. In the mouse vas deferens, this peptide is 3 times more potent than [Leu]enkephalin. Well-washed rat brain membranes degrade the peptide rapidly, suggesting the presence of a membrane-bound degradative enzyme. The peptide displays considerable immunoreactivity in assays with antisera that have been used for the immunohistochemical localization of [Leu]enkephalin. The remarkable enhancement of the potency of [Leu]enkephalin by the COOH-terminal extension -Arg-Arg-Ile-Arg-Pro-Lys-Leu-Lys-OH suggests new interpretations concerning the structure of opiate receptors and the function of the enkephalin pentapeptides.

Topics

dynorphin opioid peptide potency, Leu-enkephalin dynorphin, porcine pituitary endorphin, guinea pig ileum opioid assay, kappa opioid receptor peptide, endogenous opioid tridecapeptide, dynorphin vas deferens assay, opioid peptide pharmacology, naloxone antagonism dynorphin, neuroendocrine opioid peptide
PMID 230519 230519 DOI 10.1073/pnas.76.12.6666 10.1073/pnas.76.12.6666

Cite this article

Goldstein, A., Tachibana, S., Lowney, L. I., Hunkapiller, M., & Hood, L. (1979). Dynorphin-(1-13), an extraordinarily potent opioid peptide. *Proceedings of the National Academy of Sciences of the United States of America*, *76*(12), 6666-6670. https://doi.org/10.1073/pnas.76.12.6666

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