β-conglycinin combined with fenofibrate or rosuvastatin have exerted distinct hypocholesterolemic effects in rats

Detalhes bibliográficos
Autor(a) principal: Ferreira, Ederlan S. [UNESP]
Data de Publicação: 2012
Outros Autores: Silva, Maraiza A. [UNESP], Demonte, Aureluce [UNESP], Neves, Valdir Augusto [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
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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spelling 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:29462024-06-21T12:47:11Repositório 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
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
title_full_unstemmed 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]
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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