Vascular effects of egg white-derived peptides in resistance arteries from rats. Structure-activity relationships
BACKGROUND: The vasodilator properties of several peptide sequences derived from egg white proteins were screened in mesenteric resistance arteries from Wistar-Kyoto rats. For this, third-order branches of themesenteric arteries from6-month-old male rats were used. The vasodilator responses, with or without endothelium, to several peptides (0.1mmol L-1)wereanalysed in an isometric myograph. Moreover, the effect of nitric oxide (NO) synthase (L-NAME, 100 μmol L-1) and cyclooxygenase (indomethacin, 10 μmol L-1) inhibitors on the vasodilator response was tested. RESULTS: The peptides Arg-Ala-Asp-His-Pro-Phe-Leu, Arg-Ala-Asp-His-Pro-Phe, Arg-Ala-Asp-His-Pro, Tyr-Arg-Gly-Gly-Leu-Glu-Pro-Ile-Asn-Phe, Arg-Asp-Ile-Leu-Asn-Gln and Val-Pro-Pro showed a high endothelium-dependent vasorelaxation, whereas Phe-Arg-Ala-Asp-His-Pro-Phe-Leu was only partially endothelium-dependent. The relaxation induced by Arg-Ala-Asp-His-Pro-Phe-Leu, Arg-Ala-Asp-His-Pro-Phe, Arg-Ala-Asp-His-Pro, Arg-Asp-Ile-Leu-Asn-Gln and Val-Pro-Pro wasmainlymediated by NO, since the response was inhibited only by L-NAME, while both L-NAME and indomethacin inhibited the vasodilator response induced by Phe-Arg-Ala-Asp-His-Pro-Phe-Leu and Tyr-Arg-Gly-Gly-Leu-Glu-Pro-Ile-Asn-Phe. The presence of Arg or Tyr at the N-terminal position could be related to the vasodilator activity of these compounds in this vascular bed. The well-known angiotensin-converting enzyme inhibitor captopril showed only a slight vasodilator effect. CONCLUSION: These peptides could reduce the vascular resistance and be used as functional ingredients in the prevention and/or treatment of hypertension and other associated disorders.
Main Authors: | , , , , |
---|---|
Format: | artículo biblioteca |
Language: | English |
Published: |
Wiley-Blackwell
2010
|
Online Access: | http://hdl.handle.net/10261/50334 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
id |
dig-cial-es-10261-50334 |
---|---|
record_format |
koha |
spelling |
dig-cial-es-10261-503342018-09-19T11:29:07Z Vascular effects of egg white-derived peptides in resistance arteries from rats. Structure-activity relationships García-Redondo, Ana B. Roque, F. R. Miguel, Marta López-Fandiño, Rosina Salaices, M. BACKGROUND: The vasodilator properties of several peptide sequences derived from egg white proteins were screened in mesenteric resistance arteries from Wistar-Kyoto rats. For this, third-order branches of themesenteric arteries from6-month-old male rats were used. The vasodilator responses, with or without endothelium, to several peptides (0.1mmol L-1)wereanalysed in an isometric myograph. Moreover, the effect of nitric oxide (NO) synthase (L-NAME, 100 μmol L-1) and cyclooxygenase (indomethacin, 10 μmol L-1) inhibitors on the vasodilator response was tested. RESULTS: The peptides Arg-Ala-Asp-His-Pro-Phe-Leu, Arg-Ala-Asp-His-Pro-Phe, Arg-Ala-Asp-His-Pro, Tyr-Arg-Gly-Gly-Leu-Glu-Pro-Ile-Asn-Phe, Arg-Asp-Ile-Leu-Asn-Gln and Val-Pro-Pro showed a high endothelium-dependent vasorelaxation, whereas Phe-Arg-Ala-Asp-His-Pro-Phe-Leu was only partially endothelium-dependent. The relaxation induced by Arg-Ala-Asp-His-Pro-Phe-Leu, Arg-Ala-Asp-His-Pro-Phe, Arg-Ala-Asp-His-Pro, Arg-Asp-Ile-Leu-Asn-Gln and Val-Pro-Pro wasmainlymediated by NO, since the response was inhibited only by L-NAME, while both L-NAME and indomethacin inhibited the vasodilator response induced by Phe-Arg-Ala-Asp-His-Pro-Phe-Leu and Tyr-Arg-Gly-Gly-Leu-Glu-Pro-Ile-Asn-Phe. The presence of Arg or Tyr at the N-terminal position could be related to the vasodilator activity of these compounds in this vascular bed. The well-known angiotensin-converting enzyme inhibitor captopril showed only a slight vasodilator effect. CONCLUSION: These peptides could reduce the vascular resistance and be used as functional ingredients in the prevention and/or treatment of hypertension and other associated disorders. Peer Reviewed 2012-05-29T09:54:00Z 2012-05-29T09:54:00Z 2010 2012-05-29T09:54:00Z artículo http://purl.org/coar/resource_type/c_6501 doi: 10.1002/jsfa.4037 issn: 0022-5142 Journal of the Science of Food and Agriculture 90: 1988-1993 (2010) http://hdl.handle.net/10261/50334 10.1002/jsfa.4037 en none Wiley-Blackwell |
institution |
CIAL ES |
collection |
DSpace |
country |
España |
countrycode |
ES |
component |
Bibliográfico |
access |
En linea |
databasecode |
dig-cial-es |
tag |
biblioteca |
region |
Europa del Sur |
libraryname |
Biblioteca del CIAL España |
language |
English |
description |
BACKGROUND: The vasodilator properties of several peptide sequences derived from egg white proteins were screened in mesenteric resistance arteries from Wistar-Kyoto rats. For this, third-order branches of themesenteric arteries from6-month-old male rats were used. The vasodilator responses, with or without endothelium, to several peptides (0.1mmol L-1)wereanalysed in an isometric myograph. Moreover, the effect of nitric oxide (NO) synthase (L-NAME, 100 μmol L-1) and cyclooxygenase (indomethacin, 10 μmol L-1) inhibitors on the vasodilator response was tested. RESULTS: The peptides Arg-Ala-Asp-His-Pro-Phe-Leu, Arg-Ala-Asp-His-Pro-Phe, Arg-Ala-Asp-His-Pro, Tyr-Arg-Gly-Gly-Leu-Glu-Pro-Ile-Asn-Phe, Arg-Asp-Ile-Leu-Asn-Gln and Val-Pro-Pro showed a high endothelium-dependent vasorelaxation, whereas Phe-Arg-Ala-Asp-His-Pro-Phe-Leu was only partially endothelium-dependent. The relaxation induced by Arg-Ala-Asp-His-Pro-Phe-Leu, Arg-Ala-Asp-His-Pro-Phe, Arg-Ala-Asp-His-Pro, Arg-Asp-Ile-Leu-Asn-Gln and Val-Pro-Pro wasmainlymediated by NO, since the response was inhibited only by L-NAME, while both L-NAME and indomethacin inhibited the vasodilator response induced by Phe-Arg-Ala-Asp-His-Pro-Phe-Leu and Tyr-Arg-Gly-Gly-Leu-Glu-Pro-Ile-Asn-Phe. The presence of Arg or Tyr at the N-terminal position could be related to the vasodilator activity of these compounds in this vascular bed. The well-known angiotensin-converting enzyme inhibitor captopril showed only a slight vasodilator effect. CONCLUSION: These peptides could reduce the vascular resistance and be used as functional ingredients in the prevention and/or treatment of hypertension and other associated disorders. |
format |
artículo |
author |
García-Redondo, Ana B. Roque, F. R. Miguel, Marta López-Fandiño, Rosina Salaices, M. |
spellingShingle |
García-Redondo, Ana B. Roque, F. R. Miguel, Marta López-Fandiño, Rosina Salaices, M. Vascular effects of egg white-derived peptides in resistance arteries from rats. Structure-activity relationships |
author_facet |
García-Redondo, Ana B. Roque, F. R. Miguel, Marta López-Fandiño, Rosina Salaices, M. |
author_sort |
García-Redondo, Ana B. |
title |
Vascular effects of egg white-derived peptides in resistance arteries from rats. Structure-activity relationships |
title_short |
Vascular effects of egg white-derived peptides in resistance arteries from rats. Structure-activity relationships |
title_full |
Vascular effects of egg white-derived peptides in resistance arteries from rats. Structure-activity relationships |
title_fullStr |
Vascular effects of egg white-derived peptides in resistance arteries from rats. Structure-activity relationships |
title_full_unstemmed |
Vascular effects of egg white-derived peptides in resistance arteries from rats. Structure-activity relationships |
title_sort |
vascular effects of egg white-derived peptides in resistance arteries from rats. structure-activity relationships |
publisher |
Wiley-Blackwell |
publishDate |
2010 |
url |
http://hdl.handle.net/10261/50334 |
work_keys_str_mv |
AT garciaredondoanab vasculareffectsofeggwhitederivedpeptidesinresistancearteriesfromratsstructureactivityrelationships AT roquefr vasculareffectsofeggwhitederivedpeptidesinresistancearteriesfromratsstructureactivityrelationships AT miguelmarta vasculareffectsofeggwhitederivedpeptidesinresistancearteriesfromratsstructureactivityrelationships AT lopezfandinorosina vasculareffectsofeggwhitederivedpeptidesinresistancearteriesfromratsstructureactivityrelationships AT salaicesm vasculareffectsofeggwhitederivedpeptidesinresistancearteriesfromratsstructureactivityrelationships |
_version_ |
1777671099627077632 |