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J Physiol Biochem ; 74(4): 647-654, 2018 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-30232707

RESUMEN

To fight against metabolic disorders such as insulin resistance, new alimentary behaviors are developed. For instance, hyperproteined, gluten-free, or collagen-enriched diets could be preconized in order to reduce the consequences of obesity. In this aim, this study evaluates the potential effects of warm sea fish collagen peptides (Naticol®) on representative metabolic and inflammatory parameters. For that, male C57Bl6/J mice fed with either a chow- (CD) or high-fat diet (HFD) were submitted or not to specific collagen peptides in drinking water (4 g/kg bw/d) for 20 weeks. Weight, body composition, glucose tolerance, and insulin sensitivity were followed up. Effects of fish collagen peptides on various blood parameters reflecting the metabolism status were also measured (free fatty acids, triglycerides, cholesterol, hormones) together with adipocyte inflammation. Results showed that HFD-fed mice supplemented by fish collagen peptides exhibited a significant lower increase in body weight as soon as the twelfth week of treatment whereas no effect of the peptide was observed in CD fed mice. In line with this result, a weaker increase in fat mass in HFD-fed mice supplemented with Naticol® at both 9 and 18 weeks of treatment was also observed. In spite of this resistance to obesity promoted by fish collagen peptides treatment, no difference in glucose tolerance was found between groups whereas mice treated with Naticol® exhibited a lower basal glycemia. Also, even if no effect of the treatment on adipocyte lipolysis was found, a decrease of inflammatory cytokines was retrieved in collagen-supplemented group arguing for a potential better insulin sensitivity. Altogether, these results need to be completed but are the first describing a benefic role of warm sea fish collagen peptides in a context of metabolic disease paving the route for a potential utilization in human obesity-associated disorders.


Asunto(s)
Fármacos Antiobesidad/uso terapéutico , Colágeno/uso terapéutico , Suplementos Dietéticos , Proteínas de Peces en la Dieta/uso terapéutico , Resistencia a la Insulina , Obesidad/terapia , Fragmentos de Péptidos/uso terapéutico , Tejido Adiposo/inmunología , Tejido Adiposo/metabolismo , Animales , Antiinflamatorios no Esteroideos/efectos adversos , Antiinflamatorios no Esteroideos/química , Antiinflamatorios no Esteroideos/metabolismo , Antiinflamatorios no Esteroideos/uso terapéutico , Fármacos Antiobesidad/efectos adversos , Fármacos Antiobesidad/química , Fármacos Antiobesidad/metabolismo , Apelina/agonistas , Apelina/genética , Apelina/metabolismo , Colágeno/efectos adversos , Colágeno/química , Colágeno/metabolismo , Citocinas/antagonistas & inhibidores , Citocinas/genética , Citocinas/metabolismo , Dieta Alta en Grasa/efectos adversos , Suplementos Dietéticos/efectos adversos , Proteínas de Peces en la Dieta/efectos adversos , Proteínas de Peces en la Dieta/química , Proteínas de Peces en la Dieta/metabolismo , Regulación de la Expresión Génica , Intolerancia a la Glucosa/etiología , Intolerancia a la Glucosa/inmunología , Intolerancia a la Glucosa/prevención & control , Lipólisis , Masculino , Ratones Endogámicos C57BL , Obesidad/etiología , Obesidad/metabolismo , Obesidad/fisiopatología , Paniculitis/etiología , Paniculitis/inmunología , Paniculitis/prevención & control , Fragmentos de Péptidos/efectos adversos , Fragmentos de Péptidos/química , Fragmentos de Péptidos/metabolismo , Aumento de Peso
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