Your browser doesn't support javascript.
loading
Effects of exercise training on ANGPTL3/8 and ANGPTL4/8 and their associations with cardiometabolic traits.
Hoffmann, William G; Chen, Yan Q; Schwartz, Charles S; Barber, Jacob L; Dev, Prasun K; Reasons, Riley J; Miranda Maravi, Juan S; Armstrong, Bridget; Gerszten, Robert E; Silbernagel, Günther; Konrad, Robert J; Bouchard, Claude; Sarzynski, Mark A.
Afiliação
  • Hoffmann WG; University of South Carolina School of Medicine, Columbia, SC, USA.
  • Chen YQ; Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, USA.
  • Schwartz CS; Department of Exercise Science, University of South Carolina, Columbia, SC, USA.
  • Barber JL; Department of Exercise Science, University of South Carolina, Columbia, SC, USA; Division of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Boston, MA, USA.
  • Dev PK; Department of Exercise Science, University of South Carolina, Columbia, SC, USA.
  • Reasons RJ; Department of Exercise Science, University of South Carolina, Columbia, SC, USA.
  • Miranda Maravi JS; Department of Exercise Science, University of South Carolina, Columbia, SC, USA.
  • Armstrong B; Department of Exercise Science, University of South Carolina, Columbia, SC, USA.
  • Gerszten RE; Division of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Boston, MA, USA.
  • Silbernagel G; Division of Vascular Medicine, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
  • Konrad RJ; Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, USA.
  • Bouchard C; Human Genomics Laboratory, Pennington Biomedical Research Center, Baton Rouge, LA, USA.
  • Sarzynski MA; Department of Exercise Science, University of South Carolina, Columbia, SC, USA. Electronic address: sarz@mailbox.sc.edu.
J Lipid Res ; 65(2): 100495, 2024 02.
Article em En | MEDLINE | ID: mdl-38160757
ABSTRACT
Angiopoietin-like protein (ANGPTL) complexes 3/8 and 4/8 are established inhibitors of LPL and novel therapeutic targets for dyslipidemia. However, the effects of regular exercise on ANGPTL3/8 and ANGPTL4/8 are unknown. We characterized ANGPTL3/8 and ANGPTL4/8 and their relationship with in vivo measurements of lipase activities and cardiometabolic traits before and after a 5-month endurance exercise training intervention in 642 adults from the HERITAGE (HEalth, RIsk factors, exercise Training And GEnetics) Family Study. At baseline, higher levels of both ANGPTL3/8 and ANGPTL4/8 were associated with a worse lipid, lipoprotein, and cardiometabolic profile, with only ANGPTL3/8 associated with postheparin LPL and HL activities. ANGPTL3/8 significantly decreased with exercise training, which corresponded with increases in LPL activity and decreases in HL activity, plasma triglycerides, apoB, visceral fat, and fasting insulin (all P < 5.1 × 10-4). Exercise-induced changes in ANGPTL4/8 were directly correlated to concomitant changes in total cholesterol, LDL-C, apoB, and HDL-triglycerides and inversely related to change in insulin sensitivity index (all P < 7.0 × 10-4). In conclusion, exercise-induced decreases in ANGPTL3/8 and ANGPTL4/8 were related to concomitant improvements in lipase activity, lipid profile, and cardiometabolic risk factors. These findings reveal the ANGPTL3-4-8 model as a potential molecular mechanism contributing to adaptations in lipid metabolism in response to exercise training.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Adult / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Adult / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article