β-conglycinin combined with fenofibrate or rosuvastatin have exerted distinct hypocholesterolemic effects in rats
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
DOI: | 10.1186/1476-511X-11-11 |
Texto Completo: | http://dx.doi.org/10.1186/1476-511X-11-11 http://hdl.handle.net/11449/73170 |
Resumo: | Background: There is increasing interest in non-pharmacological control of cholesterol and triglyceride levels in the plasma and diet-drug association represent an important area of studies. The objective of this study was to observe the hypocholesterolemic effect of soybean β-conglycinin (7S protein) alone and combined with fenofibrate and rosuvastatin, two hypolipidemic drugs. Methods. The protein and drugs were administered orally once a day to rats and the effects were evaluated after 28 days. Wistar rats were divided into six groups (n = 9): hypercholesterolemic diet (HC), HC+7S protein (300 mg.kg-1 day-1) (HC-7S), HC+fenofibrate (30 mg.kg-1 day-1)(HC-FF), HC+rosuvastatin (10 mg.kg-1 day-1)(HC-RO), HC+7S+fenofibrate (HC-7S-FF) and HC+7S+rosuvastatin (HC-7S-RO). Results: Animals in HC-7S, HC-FF and HC-RO exhibited reductions of 22.9, 35.8 and 18.8% in total plasma cholesterol, respectively. In HC-7S-FF, animals did not show significant alteration of the level in HC+FF while the group HC-7S-RO showed a negative effect in comparison with groups taking only protein (HC-7S) or drug (HC-RO). The administration of the protein, fenofibrate and rosuvastatin alone caused increases in the plasma HDL-C of the animals, while the protein-drug combinations led to an increase compared to HC-FF and HC-RO. The plasma concentration of triacylgycerides was significantly reduced in the groups without association, while HC-7S-FF showed no alteration and HC-7S-RO a little reduction. Conclusion: The results of our study indicate that conglycinin has effects comparable to fenofibrate and rosuvastatin on the control of plasma cholesterol, HDL-C and triacylglycerides, when given to hypercholesterolemic rats, and suggests that the association of this protein with rosuvastatin alters the action of drug in the homeostasis of cholesterol. © 2012 Ferreira et al; licensee BioMed Central Ltd. |
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β-conglycinin combined with fenofibrate or rosuvastatin have exerted distinct hypocholesterolemic effects in ratsβ-conglycinincholesterol-lowering drugshypercholesterolemic dietrats.beta conglycininfenofibratehigh density lipoprotein cholesterolrosuvastatinsoybean proteintriacylglycerolunclassified drugbeta conglycinin protein, Glycine maxbeta-conglycinin protein, Glycine maxcholesterolfluorobenzeneglobulinhypocholesterolemic agentplant antigenpyrimidine derivativeseed storage proteinsulfonamideanimal experimentanimal modelcholesterol blood levelcontrolled studydiethypercholesterolemiahypocholesterolemiamalenonhumanrattriacylglycerol blood levelanimalblooddrug combinationdrug effectdrug potentiationheartheart muscleisolation and purificationlipid dietlivermetabolismorgan sizepathologyprotein intakesoybeanWistar ratAnimaliaGlycine maxRattusRattus norvegicusAnimalsAnticholesteremic AgentsAntigens, PlantCholesterolDiet, High-FatDietary ProteinsDrug CombinationsDrug SynergismFenofibrateFluorobenzenesGlobulinsHeartHypercholesterolemiaLiverMaleMyocardiumOrgan SizePyrimidinesRatsRats, WistarSeed Storage ProteinsSoybean ProteinsSoybeansSulfonamidesTriglyceridesBackground: There is increasing interest in non-pharmacological control of cholesterol and triglyceride levels in the plasma and diet-drug association represent an important area of studies. The objective of this study was to observe the hypocholesterolemic effect of soybean β-conglycinin (7S protein) alone and combined with fenofibrate and rosuvastatin, two hypolipidemic drugs. Methods. The protein and drugs were administered orally once a day to rats and the effects were evaluated after 28 days. Wistar rats were divided into six groups (n = 9): hypercholesterolemic diet (HC), HC+7S protein (300 mg.kg-1 day-1) (HC-7S), HC+fenofibrate (30 mg.kg-1 day-1)(HC-FF), HC+rosuvastatin (10 mg.kg-1 day-1)(HC-RO), HC+7S+fenofibrate (HC-7S-FF) and HC+7S+rosuvastatin (HC-7S-RO). Results: Animals in HC-7S, HC-FF and HC-RO exhibited reductions of 22.9, 35.8 and 18.8% in total plasma cholesterol, respectively. In HC-7S-FF, animals did not show significant alteration of the level in HC+FF while the group HC-7S-RO showed a negative effect in comparison with groups taking only protein (HC-7S) or drug (HC-RO). The administration of the protein, fenofibrate and rosuvastatin alone caused increases in the plasma HDL-C of the animals, while the protein-drug combinations led to an increase compared to HC-FF and HC-RO. The plasma concentration of triacylgycerides was significantly reduced in the groups without association, while HC-7S-FF showed no alteration and HC-7S-RO a little reduction. Conclusion: The results of our study indicate that conglycinin has effects comparable to fenofibrate and rosuvastatin on the control of plasma cholesterol, HDL-C and triacylglycerides, when given to hypercholesterolemic rats, and suggests that the association of this protein with rosuvastatin alters the action of drug in the homeostasis of cholesterol. © 2012 Ferreira et al; licensee BioMed Central Ltd.Department of Food and Nutrition School of Pharmaceutical Sciences São Paulo State University-UNESP, Araraquara, SPDepartment of Food and Nutrition School of Pharmaceutical Sciences São Paulo State University-UNESP, Araraquara, SPUniversidade Estadual Paulista (Unesp)Ferreira, Ederlan S. [UNESP]Silva, Maraiza A. [UNESP]Demonte, Aureluce [UNESP]Neves, Valdir Augusto [UNESP]2014-05-27T11:26:22Z2014-05-27T11:26:22Z2012-01-16info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://dx.doi.org/10.1186/1476-511X-11-11Lipids in Health and Disease, v. 11.1476-511Xhttp://hdl.handle.net/11449/7317010.1186/1476-511X-11-112-s2.0-848557357832-s2.0-84855735783.pdf52699697678453534031319519910419Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengLipids in Health and Disease2.663info:eu-repo/semantics/openAccess2024-06-21T12:47:11Zoai:repositorio.unesp.br:11449/73170Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T21:13:04.898203Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
β-conglycinin combined with fenofibrate or rosuvastatin have exerted distinct hypocholesterolemic effects in rats |
title |
β-conglycinin combined with fenofibrate or rosuvastatin have exerted distinct hypocholesterolemic effects in rats |
spellingShingle |
β-conglycinin combined with fenofibrate or rosuvastatin have exerted distinct hypocholesterolemic effects in rats β-conglycinin combined with fenofibrate or rosuvastatin have exerted distinct hypocholesterolemic effects in rats Ferreira, Ederlan S. [UNESP] β-conglycinin cholesterol-lowering drugs hypercholesterolemic diet rats. beta conglycinin fenofibrate high density lipoprotein cholesterol rosuvastatin soybean protein triacylglycerol unclassified drug beta conglycinin protein, Glycine max beta-conglycinin protein, Glycine max cholesterol fluorobenzene globulin hypocholesterolemic agent plant antigen pyrimidine derivative seed storage protein sulfonamide animal experiment animal model cholesterol blood level controlled study diet hypercholesterolemia hypocholesterolemia male nonhuman rat triacylglycerol blood level animal blood drug combination drug effect drug potentiation heart heart muscle isolation and purification lipid diet liver metabolism organ size pathology protein intake soybean Wistar rat Animalia Glycine max Rattus Rattus norvegicus Animals Anticholesteremic Agents Antigens, Plant Cholesterol Diet, High-Fat Dietary Proteins Drug Combinations Drug Synergism Fenofibrate Fluorobenzenes Globulins Heart Hypercholesterolemia Liver Male Myocardium Organ Size Pyrimidines Rats Rats, Wistar Seed Storage Proteins Soybean Proteins Soybeans Sulfonamides Triglycerides Ferreira, Ederlan S. [UNESP] β-conglycinin cholesterol-lowering drugs hypercholesterolemic diet rats. beta conglycinin fenofibrate high density lipoprotein cholesterol rosuvastatin soybean protein triacylglycerol unclassified drug beta conglycinin protein, Glycine max beta-conglycinin protein, Glycine max cholesterol fluorobenzene globulin hypocholesterolemic agent plant antigen pyrimidine derivative seed storage protein sulfonamide animal experiment animal model cholesterol blood level controlled study diet hypercholesterolemia hypocholesterolemia male nonhuman rat triacylglycerol blood level animal blood drug combination drug effect drug potentiation heart heart muscle isolation and purification lipid diet liver metabolism organ size pathology protein intake soybean Wistar rat Animalia Glycine max Rattus Rattus norvegicus Animals Anticholesteremic Agents Antigens, Plant Cholesterol Diet, High-Fat Dietary Proteins Drug Combinations Drug Synergism Fenofibrate Fluorobenzenes Globulins Heart Hypercholesterolemia Liver Male Myocardium Organ Size Pyrimidines Rats Rats, Wistar Seed Storage Proteins Soybean Proteins Soybeans Sulfonamides Triglycerides |
title_short |
β-conglycinin combined with fenofibrate or rosuvastatin have exerted distinct hypocholesterolemic effects in rats |
title_full |
β-conglycinin combined with fenofibrate or rosuvastatin have exerted distinct hypocholesterolemic effects in rats |
title_fullStr |
β-conglycinin combined with fenofibrate or rosuvastatin have exerted distinct hypocholesterolemic effects in rats β-conglycinin combined with fenofibrate or rosuvastatin have exerted distinct hypocholesterolemic effects in rats |
title_full_unstemmed |
β-conglycinin combined with fenofibrate or rosuvastatin have exerted distinct hypocholesterolemic effects in rats β-conglycinin combined with fenofibrate or rosuvastatin have exerted distinct hypocholesterolemic effects in rats |
title_sort |
β-conglycinin combined with fenofibrate or rosuvastatin have exerted distinct hypocholesterolemic effects in rats |
author |
Ferreira, Ederlan S. [UNESP] |
author_facet |
Ferreira, Ederlan S. [UNESP] Ferreira, Ederlan S. [UNESP] Silva, Maraiza A. [UNESP] Demonte, Aureluce [UNESP] Neves, Valdir Augusto [UNESP] Silva, Maraiza A. [UNESP] Demonte, Aureluce [UNESP] Neves, Valdir Augusto [UNESP] |
author_role |
author |
author2 |
Silva, Maraiza A. [UNESP] Demonte, Aureluce [UNESP] Neves, Valdir Augusto [UNESP] |
author2_role |
author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Ferreira, Ederlan S. [UNESP] Silva, Maraiza A. [UNESP] Demonte, Aureluce [UNESP] Neves, Valdir Augusto [UNESP] |
dc.subject.por.fl_str_mv |
β-conglycinin cholesterol-lowering drugs hypercholesterolemic diet rats. beta conglycinin fenofibrate high density lipoprotein cholesterol rosuvastatin soybean protein triacylglycerol unclassified drug beta conglycinin protein, Glycine max beta-conglycinin protein, Glycine max cholesterol fluorobenzene globulin hypocholesterolemic agent plant antigen pyrimidine derivative seed storage protein sulfonamide animal experiment animal model cholesterol blood level controlled study diet hypercholesterolemia hypocholesterolemia male nonhuman rat triacylglycerol blood level animal blood drug combination drug effect drug potentiation heart heart muscle isolation and purification lipid diet liver metabolism organ size pathology protein intake soybean Wistar rat Animalia Glycine max Rattus Rattus norvegicus Animals Anticholesteremic Agents Antigens, Plant Cholesterol Diet, High-Fat Dietary Proteins Drug Combinations Drug Synergism Fenofibrate Fluorobenzenes Globulins Heart Hypercholesterolemia Liver Male Myocardium Organ Size Pyrimidines Rats Rats, Wistar Seed Storage Proteins Soybean Proteins Soybeans Sulfonamides Triglycerides |
topic |
β-conglycinin cholesterol-lowering drugs hypercholesterolemic diet rats. beta conglycinin fenofibrate high density lipoprotein cholesterol rosuvastatin soybean protein triacylglycerol unclassified drug beta conglycinin protein, Glycine max beta-conglycinin protein, Glycine max cholesterol fluorobenzene globulin hypocholesterolemic agent plant antigen pyrimidine derivative seed storage protein sulfonamide animal experiment animal model cholesterol blood level controlled study diet hypercholesterolemia hypocholesterolemia male nonhuman rat triacylglycerol blood level animal blood drug combination drug effect drug potentiation heart heart muscle isolation and purification lipid diet liver metabolism organ size pathology protein intake soybean Wistar rat Animalia Glycine max Rattus Rattus norvegicus Animals Anticholesteremic Agents Antigens, Plant Cholesterol Diet, High-Fat Dietary Proteins Drug Combinations Drug Synergism Fenofibrate Fluorobenzenes Globulins Heart Hypercholesterolemia Liver Male Myocardium Organ Size Pyrimidines Rats Rats, Wistar Seed Storage Proteins Soybean Proteins Soybeans Sulfonamides Triglycerides |
description |
Background: There is increasing interest in non-pharmacological control of cholesterol and triglyceride levels in the plasma and diet-drug association represent an important area of studies. The objective of this study was to observe the hypocholesterolemic effect of soybean β-conglycinin (7S protein) alone and combined with fenofibrate and rosuvastatin, two hypolipidemic drugs. Methods. The protein and drugs were administered orally once a day to rats and the effects were evaluated after 28 days. Wistar rats were divided into six groups (n = 9): hypercholesterolemic diet (HC), HC+7S protein (300 mg.kg-1 day-1) (HC-7S), HC+fenofibrate (30 mg.kg-1 day-1)(HC-FF), HC+rosuvastatin (10 mg.kg-1 day-1)(HC-RO), HC+7S+fenofibrate (HC-7S-FF) and HC+7S+rosuvastatin (HC-7S-RO). Results: Animals in HC-7S, HC-FF and HC-RO exhibited reductions of 22.9, 35.8 and 18.8% in total plasma cholesterol, respectively. In HC-7S-FF, animals did not show significant alteration of the level in HC+FF while the group HC-7S-RO showed a negative effect in comparison with groups taking only protein (HC-7S) or drug (HC-RO). The administration of the protein, fenofibrate and rosuvastatin alone caused increases in the plasma HDL-C of the animals, while the protein-drug combinations led to an increase compared to HC-FF and HC-RO. The plasma concentration of triacylgycerides was significantly reduced in the groups without association, while HC-7S-FF showed no alteration and HC-7S-RO a little reduction. Conclusion: The results of our study indicate that conglycinin has effects comparable to fenofibrate and rosuvastatin on the control of plasma cholesterol, HDL-C and triacylglycerides, when given to hypercholesterolemic rats, and suggests that the association of this protein with rosuvastatin alters the action of drug in the homeostasis of cholesterol. © 2012 Ferreira et al; licensee BioMed Central Ltd. |
publishDate |
2012 |
dc.date.none.fl_str_mv |
2012-01-16 2014-05-27T11:26:22Z 2014-05-27T11:26:22Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1186/1476-511X-11-11 Lipids in Health and Disease, v. 11. 1476-511X http://hdl.handle.net/11449/73170 10.1186/1476-511X-11-11 2-s2.0-84855735783 2-s2.0-84855735783.pdf 5269969767845353 4031319519910419 |
url |
http://dx.doi.org/10.1186/1476-511X-11-11 http://hdl.handle.net/11449/73170 |
identifier_str_mv |
Lipids in Health and Disease, v. 11. 1476-511X 10.1186/1476-511X-11-11 2-s2.0-84855735783 2-s2.0-84855735783.pdf 5269969767845353 4031319519910419 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Lipids in Health and Disease 2.663 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
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1822182267487780864 |
dc.identifier.doi.none.fl_str_mv |
10.1186/1476-511X-11-11 |