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ß-Hydroxybutyrate is reduced in humans with obesity-related NAFLD and displays a dose-dependent effect on skeletal muscle mitochondrial respiration in vitro.
Mey, Jacob T; Erickson, Melissa L; Axelrod, Christopher L; King, William T; Flask, Chris A; McCullough, Arthur J; Kirwan, John P.
Afiliação
  • Mey JT; Integrated Physiology and Molecular Medicine, Pennington Biomedical Research Center, Baton Rouge, Louisiana.
  • Erickson ML; Inflammation and Immunity, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio.
  • Axelrod CL; Integrated Physiology and Molecular Medicine, Pennington Biomedical Research Center, Baton Rouge, Louisiana.
  • King WT; Inflammation and Immunity, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio.
  • Flask CA; Integrated Physiology and Molecular Medicine, Pennington Biomedical Research Center, Baton Rouge, Louisiana.
  • McCullough AJ; Inflammation and Immunity, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio.
  • Kirwan JP; Translational Services, Pennington Biomedical Research Center, Baton Rouge, Louisiana.
Am J Physiol Endocrinol Metab ; 319(1): E187-E195, 2020 07 01.
Article em En | MEDLINE | ID: mdl-32396388
Nonalcoholic fatty liver disease (NAFLD) is characterized by hepatic fat accumulation and impaired insulin sensitivity. Reduced hepatic ketogenesis may promote these pathologies, but data are inconclusive in humans and the link between NAFLD and reduced insulin sensitivity remains obscure. We investigated individuals with obesity-related NAFLD and hypothesized that ß-hydroxybutyrate (ßOHB; the predominant ketone species) would be reduced and related to hepatic fat accumulation and insulin sensitivity. Furthermore, we hypothesized that ketones would impact skeletal muscle mitochondrial respiration in vitro. Hepatic fat was assessed by 1H-MRS in 22 participants in a parallel design, case control study [Control: n = 7, age 50 ± 6 yr, body mass index (BMI) 30 ± 1 kg/m2; NAFLD: n = 15, age 57 ± 3 yr, BMI 35 ± 1 kg/m2]. Plasma assessments were conducted in the fasted state. Whole body insulin sensitivity was determined by the gold-standard hyperinsulinemic-euglycemic clamp. The effect of ketone dose (0.5-5.0 mM) on mitochondrial respiration was conducted in human skeletal muscle cell culture. Fasting ßOHB, a surrogate measure of hepatic ketogenesis, was reduced in NAFLD (-15.6%, P < 0.01) and correlated negatively with liver fat (r2 = 0.21, P = 0.03) and positively with insulin sensitivity (r2 = 0.30, P = 0.01). Skeletal muscle mitochondrial oxygen consumption increased with low-dose ketones, attributable to increases in basal respiration (135%, P < 0.05) and ATP-linked oxygen consumption (136%, P < 0.05). NAFLD pathophysiology includes impaired hepatic ketogenesis, which is associated with hepatic fat accumulation and impaired insulin sensitivity. This reduced capacity to produce ketones may be a potential link between NAFLD and NAFLD-associated reductions in whole body insulin sensitivity, whereby ketone concentrations impact skeletal muscle mitochondrial respiration.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Músculo Esquelético / Fibras Musculares Esqueléticas / Ácido 3-Hidroxibutírico / Hepatopatia Gordurosa não Alcoólica / Fígado / Mitocôndrias Musculares / Obesidade Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Músculo Esquelético / Fibras Musculares Esqueléticas / Ácido 3-Hidroxibutírico / Hepatopatia Gordurosa não Alcoólica / Fígado / Mitocôndrias Musculares / Obesidade Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article