Abstract
The hydrolytic stability of a range of cyclic tripeptides, including the therapeutically important dalargin and stemokin, as well as peptides modified by ibuprofen and aspirin, has been studied. The first two experimental systems used utilized purified enzymes (pepsin, trypsin, and chymotrypsin), while the second one utilized fragments of the stomach and small intestine of rats. The linear peptides containing only L-amino acid residues were shown to be hydrolyzed by stomach and intestine fragments, although some of these peptides were resistant to hydrolysis by individual enzymes. The peptides containing D-amino acid residues and cyclic peptides were stable under all of the conditions used, but the peptides modified by aspirin lost the acetyl group of the aspirin moiety in acidic media, this process being accelerated in the presence of pepsin.
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Abbreviations
- GIT:
-
gastrointestinal tract
- SSM:
-
artificial stomach salt mixture
- ISM:
-
artificial intestine salt mixture
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Original Russian Text © M.G. Akimov, I.V. Nazimov, N.M. Gretskaya, V.I. Deigin, V.V. Bezuglov, 2010, published in Bioorganicheskaya Khimiya, 2010, Vol. 36, No. 6, pp. 753–759.
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Akimov, M.G., Nazimov, I.V., Gretskaya, N.M. et al. Investigation of peptide stability upon hydrolysis by of fragments of the organs of the gastrointestinal tract of rats. Russ J Bioorg Chem 36, 690–695 (2010). https://doi.org/10.1134/S1068162010060038
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DOI: https://doi.org/10.1134/S1068162010060038