β-conglycinin combined with fenofibrate or rosuvastatin have exerted distinct hypocholesterolemic effects in rats
Contribuinte(s) |
Universidade Estadual Paulista (UNESP) |
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Data(s) |
27/05/2014
27/05/2014
16/01/2012
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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. |
Identificador |
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 |
Idioma(s) |
eng |
Relação |
Lipids in Health and Disease |
Direitos |
openAccess |
Palavras-Chave | #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 |
Tipo |
info:eu-repo/semantics/article |