posted on 2021-09-20, 16:58authored byMaria M. Glavas, Ann Y. Lee, Ian Miao, Fan Yang, Majid Mojibian, Shannon M. O’Dwyer, Timothy J. Kieffer
We
previously demonstrated that male, but not female, Swiss Webster mice are
susceptible to diabetes, with incidence increased by early overnutrition and
high-fat diet (HFD). Here, we investigated how HFD in Swiss Webster males and
females during preweaning, peripubertal, and post-pubertal periods alters
glucose homeostasis and diabetes susceptibility. In males, HFD throughout life
resulted in the highest diabetes incidence. Notably, switching to chow post-puberty
was protective against diabetes relative to switching to chow at weaning,
despite the longer period of HFD exposure. Similarly, HFD throughout life in
males resulted in less liver steatosis relative to mice with shorter duration
of postpubertal HFD. Thus, HFD timing relative to weaning and puberty, not
simply exposure length, contributes to metabolic outcomes. Females were
protected from hyperglycemia regardless of length or timing of HFD. However,
postpubertal HFD resulted in a high degree of hepatic steatosis and adipose
fibrosis, but glucose regulation and insulin sensitivity remained unchanged Interestingly,
peri-insulitis was observed in the majority of females but was not correlated
with impaired glucose regulation. Our findings reveal critical periods of
HFD-induced glucose dysregulation with striking sex differences in Swiss
Webster mice, highlighting the importance of careful consideration of HFD timing
relative to critical developmental periods.
Funding
This work was supported by a grant from the Canadian Institutes of Health Research.