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Modulation of the Pharmacological Activities of Secretory Phospholipase A2 from Crotalus durissus cascavella Induced by Naringin

In this work we have characterized the action of the naringin, a flavonoid found in grapefruit and known for its various pharmacological effects, which include antioxidant, blood lipid lowering and anticancer activity, on the structure and biochemical activities of a secretory phospholipase A (sPLA2...

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Autores principales: Santos, Marcelo L., Toyama, Daniela O., Oliveira, Simone C. B., Cotrim, Camila A., Diz-Filho, Eduardo B. S., Fagundes, Fábio H. R., Soares, Veronica C. G., Aparicio, Ricardo, Toyama, Marcos H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259155/
https://www.ncbi.nlm.nih.gov/pubmed/21245808
http://dx.doi.org/10.3390/molecules16010738
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author Santos, Marcelo L.
Toyama, Daniela O.
Oliveira, Simone C. B.
Cotrim, Camila A.
Diz-Filho, Eduardo B. S.
Fagundes, Fábio H. R.
Soares, Veronica C. G.
Aparicio, Ricardo
Toyama, Marcos H.
author_facet Santos, Marcelo L.
Toyama, Daniela O.
Oliveira, Simone C. B.
Cotrim, Camila A.
Diz-Filho, Eduardo B. S.
Fagundes, Fábio H. R.
Soares, Veronica C. G.
Aparicio, Ricardo
Toyama, Marcos H.
author_sort Santos, Marcelo L.
collection PubMed
description In this work we have characterized the action of the naringin, a flavonoid found in grapefruit and known for its various pharmacological effects, which include antioxidant, blood lipid lowering and anticancer activity, on the structure and biochemical activities of a secretory phospholipase A (sPLA2) from Crotalus durissus cascavella, an important protein involved in the releasinge of arachidonic acid in phospholipid membranes. sPLA2 was incubated with naringin (mol:mol) at 37 °C and a discrete reduction in the UV scanning signal and a modification of the circular dichroism spectra were observed after treatment with naringin, suggesting modifications of the secondary structure of the protein. This flavonoid was able to decrease enzymatic activity and some pharmacological effects, such as myonecrosis, platelet aggregation, and neurotoxic activity caused by sPLA2, however, the inflammatory effect was not affected by naringin. In addition, small angle X-ray scattering (SAXS) data were collected for sPLA2 and naringin-treated sPLA2 to evaluate possible modifications of the protein structure. These structural investigations have shown that sPLA2 is an elongated dimer in solution and after treatment with naringin a conformational change in the dimeric configuration was observed. Our results suggest that structural modification may be correlated with the loss of enzymatic activity and alterations in pharmacological properties.
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spelling pubmed-62591552018-12-07 Modulation of the Pharmacological Activities of Secretory Phospholipase A2 from Crotalus durissus cascavella Induced by Naringin Santos, Marcelo L. Toyama, Daniela O. Oliveira, Simone C. B. Cotrim, Camila A. Diz-Filho, Eduardo B. S. Fagundes, Fábio H. R. Soares, Veronica C. G. Aparicio, Ricardo Toyama, Marcos H. Molecules Article In this work we have characterized the action of the naringin, a flavonoid found in grapefruit and known for its various pharmacological effects, which include antioxidant, blood lipid lowering and anticancer activity, on the structure and biochemical activities of a secretory phospholipase A (sPLA2) from Crotalus durissus cascavella, an important protein involved in the releasinge of arachidonic acid in phospholipid membranes. sPLA2 was incubated with naringin (mol:mol) at 37 °C and a discrete reduction in the UV scanning signal and a modification of the circular dichroism spectra were observed after treatment with naringin, suggesting modifications of the secondary structure of the protein. This flavonoid was able to decrease enzymatic activity and some pharmacological effects, such as myonecrosis, platelet aggregation, and neurotoxic activity caused by sPLA2, however, the inflammatory effect was not affected by naringin. In addition, small angle X-ray scattering (SAXS) data were collected for sPLA2 and naringin-treated sPLA2 to evaluate possible modifications of the protein structure. These structural investigations have shown that sPLA2 is an elongated dimer in solution and after treatment with naringin a conformational change in the dimeric configuration was observed. Our results suggest that structural modification may be correlated with the loss of enzymatic activity and alterations in pharmacological properties. MDPI 2011-01-18 /pmc/articles/PMC6259155/ /pubmed/21245808 http://dx.doi.org/10.3390/molecules16010738 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Santos, Marcelo L.
Toyama, Daniela O.
Oliveira, Simone C. B.
Cotrim, Camila A.
Diz-Filho, Eduardo B. S.
Fagundes, Fábio H. R.
Soares, Veronica C. G.
Aparicio, Ricardo
Toyama, Marcos H.
Modulation of the Pharmacological Activities of Secretory Phospholipase A2 from Crotalus durissus cascavella Induced by Naringin
title Modulation of the Pharmacological Activities of Secretory Phospholipase A2 from Crotalus durissus cascavella Induced by Naringin
title_full Modulation of the Pharmacological Activities of Secretory Phospholipase A2 from Crotalus durissus cascavella Induced by Naringin
title_fullStr Modulation of the Pharmacological Activities of Secretory Phospholipase A2 from Crotalus durissus cascavella Induced by Naringin
title_full_unstemmed Modulation of the Pharmacological Activities of Secretory Phospholipase A2 from Crotalus durissus cascavella Induced by Naringin
title_short Modulation of the Pharmacological Activities of Secretory Phospholipase A2 from Crotalus durissus cascavella Induced by Naringin
title_sort modulation of the pharmacological activities of secretory phospholipase a2 from crotalus durissus cascavella induced by naringin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259155/
https://www.ncbi.nlm.nih.gov/pubmed/21245808
http://dx.doi.org/10.3390/molecules16010738
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