Key result
Prenatal malnutrition primarily affected perirenal adipose tissue in males, reducing expandability and predisposing them to obesity-associated metabolic risks.
Why the study?
The study aimed to investigate the long-term, tissue- and sex-specific impacts of pre- and postnatal malnutrition on the expandability and functional traits of different adipose tissues.
Does pre and postnatal malnutrition affect long-term adipose tissue expandability and functional traits in a sex-specific manner in a sheep model?
Does pre and postnatal malnutrition affect long-term adipose tissue expandability and functional traits in a sex-specific manner in a sheep model?
Pre- and postnatal malnutrition have distinct, depot- and sex-specific long-term effects on adipose tissue expandability, with epicardial fat specifically targeted by early postnatal obesity.
Sex- and depot-specific adipose effects of early malnutrition in sheep leave open human cardiometabolic translation; prospective studies needed.
The aim was to investigate long-term, tissue and sex-specific impacts of pre and postnatal malnutrition on expandability and functional traits of different adipose tissues. Twin-pregnant ewes were fed NORM (~requirements), LOW (50% of NORM) or HIGH (150%/110% of energy/protein) diets the last 6 weeks prepartum (term ~147-days). Lambs received moderate, low-fat (CONV) or high-carbohydrate-high-fat (HCHF) diets from 3 days until 6 months of age, and thereafter CONV diet. At 2½ years of age (adulthood), histomorphometric and gene expression patterns were characterized in subcutaneous (SUB), perirenal (PER), mesenteric (MES), and epicardial (EPI) adipose tissues. SUB had sex-specific (♂<♀) upper-limits for adipocyte size and cell-number indices, irrespective of early life nutrition. PER mass and contents of adipocytes were highest in females and HIGH♂, whereas adipocyte cross-sectional area was lowest in LOW♂. Pre/postnatal nutrition affected gene expression sex-specifically in SUB + PER, but unrelated to morphological changes. In PER, LOW/LOW♂ were specific targets of gene expression changes. EPI was affected by postnatal nutrition, and HCHF sheep had enlarged adipocytes and upregulated expressions for adipogenic and lipogenic genes. Conclusion: upper-limits for SUB expandability were markedly lower in males. Major targets for prenatal malnutrition were PER and males. LOW♂ had the lowest PER expandability, whereas HIGH♂ had an adaptive advantage due to increased hypertrophic ability equivalent to females. Fixed expandability in SUB meant PER became a determining factor for MES and ectopic fat deposition, rendering LOW♂ particularly predisposed for obesity-associated metabolic risks. EPI, in contrast to other tissues, was targeted particularly by early postnatal obesity, resulting in adipocyte hypertrophy in adulthood.
No takes yet. Share an insight, caveat, or question.
Ahmad et al. (2020) studied Pre and postnatal malnutrition. Pre and postnatal malnutrition diets vs. NORM prepartum; CONV postpartum was evaluated on Adipose tissue expandability and functional traits (histomorphometric and gene expression patterns). Prenatal malnutrition primarily affected perirenal adipose tissue in males, reducing expandability and predisposing them to obesity-associated metabolic risks.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: