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1.
Adv Exp Med Biol ; 975 Pt 1: 413-433, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28849472

RESUMEN

Taurine ameliorates changes occurring in newborn skeletal muscle as a result of gestational protein restriction in C57BL/6 mice, but taurine supplementation effects may be exaggerated in C57BL/6 mice due to their inherent excessive taurinuria.We examined if maternal taurine supplementation could ameliorate changes in gene expression levels, properties of mitochondria, myogenesis, and nutrient transport and sensing, in male newborn skeletal muscle caused by a maternal low protein (LP) diet in Wistar rats.LP diet resulted in an 11% non-significant decrease in birth weight, which was not rescued by taurine supplementation (LP-Tau). LP-Tau offspring had significantly lower birth weight compared to controls. Gene expression profiling revealed 895 significantly changed genes, mainly an LP-induced down-regulation of genes involved in protein translation. Taurine fully or partially rescued 32% of these changes, but with no distinct pattern as to which genes were rescued.Skeletal muscle taurine content in LP-Tau offspring was increased, but no changes in mRNA levels of the taurine synthesis pathway were observed. Taurine transporter mRNA levels, but not protein levels, were increased by LP diet.Nutrient sensing signaling pathways were largely unaffected in LP or LP-Tau groups, although taurine supplementation caused a decrease in total Akt and AMPK protein levels. PAT4 amino acid transporter mRNA was increased by LP, and normalized by taurine supplementation.In conclusion, gestational protein restriction in rats decreased genes involved in protein translation in newborn skeletal muscle and led to changes in nutrient transporters. Taurine partly rescued these changes, hence underscoring the importance of taurine in development.


Asunto(s)
Dieta con Restricción de Proteínas/efectos adversos , Músculo Esquelético/efectos de los fármacos , Efectos Tardíos de la Exposición Prenatal , Taurina/farmacología , Transcriptoma/genética , Animales , Femenino , Masculino , Mitocondrias/efectos de los fármacos , Músculo Esquelético/metabolismo , Embarazo , Ratas , Ratas Wistar
2.
Adv Exp Med Biol ; 776: 39-50, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23392869

RESUMEN

The nonprotein amino acid taurine has been shown to counteract the negative effects of a high-fructose diet in rats with regard to insulin resistance and dyslipidemia. Here we examined the long-term (26 weeks) effects of oral taurine supplementation (2% in the drinking water) in fructose-fed Wistar rats.The combination of fructose and taurine caused a significant increase in fasting glucose compared to the control diet without changing hepatic phosphoenol pyruvate carboxykinase mRNA levels. The combination of fructose and taurine also improved glucose tolerance compared to control. Neither a high-fructose diet nor taurine supplementation induced significant changes in body weight, body fat or total calorie intake, fasting insulin levels, HOMA-IR, or insulin-induced Akt phosphorylation in skeletal muscle.Fructose alone caused a decrease in liver triglyceride content, with taurine supplementation preventing this. There was no effect of long-term fructose diet and/or taurine supplementation on plasma triglycerides, plasma nonesterified fatty acids, as well as plasma HDL, LDL, and total cholesterol.In conclusion, the study suggests that long-term taurine supplementation improves glucose tolerance and normalize hepatic triglyceride content following long-term fructose feeding. However, as the combination of taurine and fructose also increased fasting glucose levels, the beneficial effect of taurine supplementation towards amelioration of glucose intolerance and insulin resistance may be questionable.


Asunto(s)
Conducta Alimentaria/efectos de los fármacos , Fructosa/farmacología , Glucosa/metabolismo , Homeostasis/efectos de los fármacos , Metabolismo de los Lípidos/efectos de los fármacos , Taurina/farmacología , Animales , Peso Corporal/efectos de los fármacos , Suplementos Dietéticos , Conducta de Ingestión de Líquido/efectos de los fármacos , Fructosa/administración & dosificación , Prueba de Tolerancia a la Glucosa , Insulina/metabolismo , Masculino , Ratas , Ratas Wistar , Transducción de Señal/efectos de los fármacos , Taurina/administración & dosificación , Factores de Tiempo
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