Search bioRxivSearch

Biology subjects

Salerno, V.

Publications and source records attributed to Salerno, V..

2 recordsLinked to original sources

Hexokinase: A central player in the synergism of high-intensity intermittent exercise and every-other-day intermittent fasting regimen on energy metabolism adaptations

Visceral lipid accumulation, organ hypertrophy and a reduction in skeletal muscle strength are all signs associated with the severity of obesity related disease. Intermittent fasting (IF) and high-intensity intermittent exercise (HIIE) are natural strategies that, individually, can prevent and ameliorate obesity along with metabolic syndrome and its associated diseases. However, the combinatorial effect of IF and HIIF on energetic metabolism is currently not well understood. We hypothesized that their combination could have a potential for more than strictly additive benefits. Here, we show that two months of every-other-day intermittent fasting regimen combined with a high-intensity intermittent exercise protocol (IF/HIIE) produce a synergetic effect, preventing fat accumulation, enhancing physical performance and optimizing energy production. The IF/HIIE group presented increased glucose uptake, lower levels of serum insulin and a global activation of hexokinases in skeletal muscle, heart and liver comparing to control, IF and HIIE groups. IF/HIIE synergism led to activation of the FoF1 ATP synthase and promoted a more oxidative profile of mitochondria in observed skeletal muscle. Additionally, high-resolution respirometry of muscle fibers showed that animals in the IF/HIIE group presented characteristics suggestive of augmented mitochondrial mass and efficiency. Finally, an important reduction in serum oxidative stress markers were observed in IF/HIIE group. These findings provide new insights for the implementation of non-pharmaceutical strategies to prevent/treat metabolic syndrome and associated diseases.

biochemistry

Genetic architecture of early childhood growth phenotypes gives insights into their link with later obesity

Early childhood growth patterns are associated with adult metabolic health, but the underlying mechanisms are unclear. We performed genome-wide meta-analyses and follow-up in up to 22,769 European children for six early growth phenotypes derived from longitudinal data: peak height and weight velocities, age and body mass index (BMI) at adiposity peak (AP ~9 months) and rebound (AR ~5-6 years). We identified four associated loci (P< 5x10-8): LEPR/LEPROT with BMI at AP, FTO and TFAP2B with Age at AR and GNPDA2 with BMI at AR. The observed AR-associated SNPs at FTO, TFAP2B and GNPDA2 represent known adult BMI-associated variants. The common BMI at AP associated variant at LEPR/LEPROT was not associated with adult BMI but was associated with LEPROT gene expression levels, especially in subcutaneous fat (P<2x10-51). We identify strong positive genetic correlations between early growth and later adiposity traits, and analysis of the full discovery stage results for Age at AR revealed enrichment for insulin-like growth factor 1 (IGF-1) signaling and apolipoprotein pathways. This genome-wide association study suggests mechanistic links between early childhood growth and adiposity in later childhood and adulthood, highlighting these early growth phenotypes as potential targets for the prevention of obesity.

genomics