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Title: Design, Synthesis and Pharmacological Characterization of Endomorphin Analogues with Non-Cyclic Amino Acid Residues in Position 2
Authors: Perlikowska, Renata ×
Fichna, Jakub
Wyrebska, Anna
Poels, Jeroen
Vanden Broeck, Jozef
Toth, Geza
Storr, Martin
do Rego, Jean-Claude
Janecka, Anna #
Issue Date: Feb-2010
Publisher: Nordic Pharmacological Society
Series Title: Basic & Clinical Pharmacology & Toxicology vol:106 issue:2 pages:106-113
Abstract: A series of endomorphin-1 (EM-1) and endomorphin-2 (EM-2) analogues, containing non-cyclic amino acids (Ala, d-Ala, β-Ala, NMeAla, d-NMeAla or Sar) instead of Pro in position 2 was synthesized, where NMeAla = N-methylalanine and Sar = N-methylglycine, sarcosine. The opioid activity profiles of these peptides were determined in μ and δ opioid receptor (MOR and DOR)-representative binding assays and bioassays in vitro, as well as in the mouse hot-plate test in vivo. Finally, the degradation rates of all analogues in the presence of either rat brain homogenate or selected proteolytic enzymes were determined. Analogues of EM-2 were generally more potent than the respective analogues of EM-1. EM-2 analogues with d-Ala or d-NMeAla were about twofold more potent than the parent peptide and were least prone to degradation by brain homogenate, dipeptydyl peptidase IV and aminopeptidase M. In the in vivo test, [d-Ala2]EM-2 and [d-NMeAla2]EM-2 showed much higher analgesic potency than EM-2 which confirmed the usefulness of structural modifications in obtaining new leads for pain-relief therapeutics.
ISSN: 1742-7835
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Animal Physiology and Neurobiology Section - miscellaneous
× corresponding author
# (joint) last author

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