Maternal obesity exacerbates insulitis and type 1 diabetes in non-obese diabetic mice

Hui Wang1, Yansong Xue2, Baolin Wang2

  • 1School of Food ScienceWashington State University, Pullman, Washington 99164, USADepartment of Animal ScienceUniversity of Wyoming, Laramie, Wyoming 82071, USADepartment of Animal SciencesWashington State University, Pullman, Washington 99164, USASchool of Food ScienceUniversity of Idaho, Moscow, Idaho 83844, USASchool of Food ScienceWashington State University, Pullman, Washington 99164, USADepartment of Animal ScienceUniversity of Wyoming, Laramie, Wyoming 82071, USADepartment of Animal SciencesWashington State University, Pullman, Washington 99164, USASchool of Food ScienceUniversity of Idaho, Moscow, Idaho 83844, USA.

Reproduction (Cambridge, England)
|April 3, 2014
PubMed

Accompanying the dramatic increase in maternal obesity, the incidence of type 1 diabetes (T1D) in children is also rapidly increasing. The objective of this study was to explore the effects of maternal obesity on the incidence of T1D in offspring using non-obese diabetic (NOD) mice, a common model for TID. Four-week-old female NOD mice were fed either a control diet (10% energy from fat, CON) or a high-fat diet (60% energy from fat) for 8 weeks before mating. Mice were maintained in their respective diets during pregnancy and lactation. All offspring mice were fed the CON to 16 weeks. Female offspring (16-week-old) born to obese dams showed more severe islet lymphocyte infiltration (major manifestation of insulitis) (P<0.01), concomitant with elevated nuclear factor kappa-light-chain-enhancer of activated B cells p65 signaling (P<0.01) and tumor necrosis factor alpha protein level (P<0.05) in the pancreas. In addition, maternal obesity resulted in impaired (P<0.05) glucose tolerance and lower (P<0.05) serum insulin levels in offspring. In conclusion, maternal obesity resulted in exacerbated insulitis and inflammation in the pancreas of NOD offspring mice, providing a possible explanation for the increased incidence of T1D in children.

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