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1.
Clin Nutr ESPEN ; 32: 1-7, 2019 08.
Artículo en Inglés | MEDLINE | ID: mdl-31221273

RESUMEN

Vinegar intake is considered a food item that improves blood glucose in humans. This review aimed to discuss studies that investigated the impact of vinegar intake on the glycemic profile in humans and the putative mechanistic cellular pathways in both human and animal models. A search of literature was performed on the Cochrane, MEDLINE and Web of Science databases for articles published between 1995 and 2018. There is considerable support for vinegar having a positive acute effect on blood glucose levels when combined with carbohydrate-rich meals. Conversely, there are few chronic interventions analyzing the impact of vinegar intake on blood glucose. Based on available evidence, we hypothesize three pathways by which vinegar may improve blood glucose: The inhibition of α-amylase action; increased glucose uptake; and mediation by transcription factors. When evaluating the current body of literature, daily vinegar intake in amounts of ∼10-30 mL (∼2-6 tablespoons) appear to improve the glycemic response to carbohydrate-rich meals; however, there is a paucity of studies investigating chronic effects of vinegar intake.


Asunto(s)
Ácido Acético/farmacología , Glucemia/efectos de los fármacos , Diabetes Mellitus Tipo 2 , Ácido Acético/administración & dosificación , Glucemia/metabolismo , Suplementos Dietéticos , Humanos , Fenómenos Fisiológicos de la Nutrición , Periodo Posprandial
2.
Nutrition ; 28(4): 465-71, 2012 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-22079394

RESUMEN

OBJECTIVE: We aimed to evaluate the effects of resistance exercise (RE) and leucine (LEU) supplementation on dexamethasone (DEXA)-induced muscle atrophy and insulin resistance. METHODS: Male Wistar rats were randomly divided into DEXA (DEX), DEXA + RE (DEX-RE), DEXA + LEU (DEX-LEU), and DEXA + RE + LEU (DEX-RE-LEU) groups. Each group received DEXA 5 mg · kg(-1) · d(-1) for 7 d from drinking water and were pair-fed to the DEX group; LEU-supplemented groups received 0.135 g · kg(-1) · d(-1) through gavage for 7 d; the RE protocol was based on three sessions of squat-type exercise composed by three sets of 10 repetitions at 70% of maximal voluntary strength capacity. RESULTS: The plantaris mass was significantly greater in both trained groups compared with the non-trained groups. Muscle cross-sectional area and fiber areas did not differ between groups. Both trained groups displayed significant increases in the number of intermediated fibers (IIa/IIx), a decreased number of fast-twitch fibers (IIb), an increased ratio of the proteins phospho(Ser2448)/total mammalian target of rapamycin and phospho(Thr389)/total 70-kDa ribosomal protein S6 kinase, and a decreased ratio of phospho(Ser253)/total Forkhead box protein-3a. Plasma glucose was significantly increased in the DEX-LEU group compared with the DEX group and RE significantly decreased hyperglycemia. The DEX-LEU group displayed decreased glucose transporter-4 translocation compared with the DEX group and RE restored this response. LEU supplementation worsened insulin sensitivity and did not attenuate muscle wasting in rats treated with DEXA. Conversely, RE modulated glucose homeostasis and fiber type transition in the plantaris muscle. CONCLUSION: Resistance exercise but not LEU supplementation promoted fiber type transition and improved glucose homeostasis in DEXA-treated rats.


Asunto(s)
Glucemia/metabolismo , Resistencia a la Insulina/fisiología , Leucina/farmacología , Músculo Esquelético , Atrofia Muscular/prevención & control , Condicionamiento Físico Animal/fisiología , Entrenamiento de Fuerza , Animales , Dexametasona , Suplementos Dietéticos , Transportador de Glucosa de Tipo 4/metabolismo , Hiperglucemia/metabolismo , Hiperglucemia/prevención & control , Masculino , Movimiento/fisiología , Fuerza Muscular/efectos de los fármacos , Fuerza Muscular/fisiología , Músculo Esquelético/anatomía & histología , Músculo Esquelético/citología , Músculo Esquelético/fisiología , Atrofia Muscular/inducido químicamente , Atrofia Muscular/metabolismo , Distribución Aleatoria , Ratas , Ratas Wistar , Proteínas Quinasas S6 Ribosómicas 70-kDa/metabolismo
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