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Biosci Biotechnol Biochem ; 67(3): 532-9, 2003 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-12723600

RESUMO

Simmondsin was modified with acarviosine-glucose using the transglycosylation activity of Thermus maltogenic amylase to synthesize a novel compound with both antiobesity and hypoglycemic activity. The LC/MS and 13C NMR analyses confirmed that the structure of the major transglycosylation product was acarviosine-simmondsin (Acv-simmondsin), in which acarviosine was attached to the glucose moiety of simmondsin by an alpha-(1,6)-glycosidic linkage. It was found that Acv-simmondsin was a potent competitive inhibitor of alpha-glucosidase with the Ki value of 0.69 microM and a mixed type inhibitor of alpha-amylase with the Ki and KI of 20.78 microM and 26.31 microM, respectively. The administration of Acv-simmondsin (0.1 g/100 g diet/day) to mice for 5 days significantly reduced food intake by 35%, compared to 25% with simmondsin in control obese mice. Acv-simmondsin (50 mg/kg BW) suppressed the postprandial blood glucose response to sucrose (1 g/kg BW) by 74%, compared to 71% with acarbose, in normal rats.


Assuntos
Acetonitrilas/metabolismo , Acetonitrilas/farmacologia , Amino Açúcares/metabolismo , Amino Açúcares/farmacologia , Cicloexanos , Ingestão de Alimentos/efeitos dos fármacos , Glucosídeos/metabolismo , Glucosídeos/farmacologia , Glicosídeo Hidrolases/metabolismo , Hiperglicemia/metabolismo , Thermus/enzimologia , Acetonitrilas/química , Amino Açúcares/química , Animais , Fármacos Antiobesidade/farmacologia , Glicemia/análise , Glicemia/efeitos dos fármacos , Peso Corporal , Sequência de Carboidratos , Glucose/análogos & derivados , Glucosídeos/química , Inibidores de Glicosídeo Hidrolases , Glicosilação , Hidrólise , Hipoglicemiantes/farmacologia , Dados de Sequência Molecular , Período Pós-Prandial , Ratos , Ratos Sprague-Dawley , Suínos , alfa-Amilases/antagonistas & inibidores
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