Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9014903 | Pharmacological Research | 2005 | 7 Pages |
Abstract
The activity of short porcine galanin (Gal) analogues was tested in vitro using rat jejunal and colonic smooth muscle strips. Peptides evoked concentration-dependent tissue contractions yielding typical response curves in concentration range from 0.3 nM to 300 μM, with a characteristic fall-down effect at the supramaximal concentrations. Gal(1-15) was less potent than Gal(1-29). Furthermore, [d-Trp2]Gal(1-15), [endo-Trp2,Cle4]Gal(1-15), [d-Leu4]Gal(1-15), [des-Leu4]Gal(1-15), [Hse6]Gal(1-15), [Dab14]Gal(1-15), [Dpr14]Gal(1-15) or [Arg14]Gal(1-15) showed a considerable decrease in potency compared to Gal(1-15) in jejunal and/or colonic smooth muscle cells. Functional evidence confirmed that the integrity of both N- and C-terminals must be preserved in order to preserve a full excitatory myogenic potential of the peptide in rat jejunum and colon. Besides, amino acids located in positions 2, 4, 6 and 14 play a crucial role in recognition and activation of molecular domains responsible for Gal action in the intestinal smooth muscle.
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Authors
A. Umer, H. Åugowska, J. Sein-Anand, P. Rekowski, J. RuczyÅski, J. Petrusewicz, R.P. Korolkiewicz,