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Chronic administration of hydrolysed pine nut oil to mice improves insulin sensitivity and glucose tolerance and increases energy expenditure via a free fatty acid receptor 4-dependent mechanism.
Wargent, Edward Taynton; Kepczynska, Malgorzata A; Kaspersen, Mads H; Ulven, Elisabeth Rexen; Arch, Jonathan R S; Ulven, Trond; Stocker, Claire Joanne.
Afiliação
  • Wargent ET; Institute of Translational Medicine, Clore Laboratory, University of Buckingham, Buckingham, MK18 1EG, UK.
  • Kepczynska MA; Institute of Translational Medicine, Clore Laboratory, University of Buckingham, Buckingham, MK18 1EG, UK.
  • Kaspersen MH; Department of Physics, Chemistry and Pharmacy, University of Southern Denmark, 5230 Odense, Denmark.
  • Ulven ER; Department of Drug Design and Pharmacology, University of Copenhagen, 2100Copenhagen, Denmark.
  • Arch JRS; Institute of Translational Medicine, Clore Laboratory, University of Buckingham, Buckingham, MK18 1EG, UK.
  • Ulven T; Department of Physics, Chemistry and Pharmacy, University of Southern Denmark, 5230 Odense, Denmark.
  • Stocker CJ; Department of Drug Design and Pharmacology, University of Copenhagen, 2100Copenhagen, Denmark.
Br J Nutr ; 132(1): 13-20, 2024 Jul 14.
Article em En | MEDLINE | ID: mdl-38751244
ABSTRACT
A healthy diet is at the forefront of measures to prevent type 2 diabetes. Certain vegetable and fish oils, such as pine nut oil (PNO), have been demonstrated to ameliorate the adverse metabolic effects of a high-fat diet. The present study investigates the involvement of the free fatty acid receptors 1 (FFAR1) and 4 (FFAR4) in the chronic activity of hydrolysed PNO (hPNO) on high-fat diet-induced obesity and insulin resistance. Male C57BL/6J wild-type, FFAR1 knockout (-/-) and FFAR4-/- mice were placed on 60 % high-fat diet for 3 months. Mice were then dosed hPNO for 24 d, during which time body composition, energy intake and expenditure, glucose tolerance and fasting plasma insulin, leptin and adiponectin were measured. hPNO improved glucose tolerance and decreased plasma insulin in the wild-type and FFAR1-/- mice, but not the FFAR4-/- mice. hPNO also decreased high-fat diet-induced body weight gain and fat mass, whilst increasing energy expenditure and plasma adiponectin. None of these effects on energy balance were statistically significant in FFAR4-/- mice, but it was not shown that they were significantly less than in wild-type mice. In conclusion, chronic hPNO supplementation reduces the metabolically detrimental effects of high-fat diet on obesity and insulin resistance in a manner that is dependent on the presence of FFAR4.
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Texto completo: 1 Temas: ECOS / Financiamentos_gastos Bases de dados: MEDLINE Assunto principal: Óleos de Plantas / Resistência à Insulina / Camundongos Knockout / Pinus / Receptores Acoplados a Proteínas G / Metabolismo Energético / Dieta Hiperlipídica / Insulina / Camundongos Endogâmicos C57BL / Obesidade Limite: Animals Idioma: En Revista: Br J Nutr Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Temas: ECOS / Financiamentos_gastos Bases de dados: MEDLINE Assunto principal: Óleos de Plantas / Resistência à Insulina / Camundongos Knockout / Pinus / Receptores Acoplados a Proteínas G / Metabolismo Energético / Dieta Hiperlipídica / Insulina / Camundongos Endogâmicos C57BL / Obesidade Limite: Animals Idioma: En Revista: Br J Nutr Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido