Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2007311 | Peptides | 2008 | 6 Pages |
Abstract
The morphiceptin-derived peptide [Dmt1, d-1-Nal3]morphiceptin, labeled μ-opioid receptor (MOP) with very high affinity and selectivity in the receptor binding assays. In the mouse hot plate test, [Dmt1, d-1-Nal3]morphiceptin given intracerebroventricularly (i.c.v.) produced profound supraspinal analgesia, being approximately 100-fold more potent than the endogenous MOP receptor ligand, endomorphin-2. The antinociceptive effect of this new analog lasted up to 120 min. Thus, [Dmt1, d-1-Nal3]morphiceptin is an interesting and extraordinarily potent analgesic, raising the possibility of novel approaches in the design of clinically useful drugs for pain treatment.
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Authors
Jakub Fichna, Jean-Claude do-Rego, Nga N. Chung, Jean Costentin, Peter W. Schiller, Anna Janecka,