Fetal hyperglycemia and a high fat diet contribute to aberrant glucose tolerance and hematopoiesis in adulthood

dc.contributor.authorBlue, Emily K.
dc.contributor.authorBallman, Kimberly
dc.contributor.authorBoyle, Frances
dc.contributor.authorOh, Eunjin
dc.contributor.authorKono, Tatsuyoshi
dc.contributor.authorQuinney, Sara K.
dc.contributor.authorThurmond, Debbie C.
dc.contributor.authorEvans-Molina, Carmella
dc.contributor.authorHaneline, Laura S.
dc.contributor.departmentDepartment of Pediatrics, IU School of Medicineen_US
dc.date.accessioned2016-03-09T17:00:28Z
dc.date.available2016-03-09T17:00:28Z
dc.date.issued2015-02
dc.description.abstractBackground Children exposed to gestational diabetes mellitus (GDM) during pregnancy are at increased risk of obesity, diabetes, and hypertension. Our goal was to identify metabolic and hematopoietic alterations after intrauterine exposure to maternal hyperglycemia that may contribute to the pathogenesis of chronic morbidities. Methods Streptozotocin treatment induced maternal hyperglycemia during the last third of gestation in rat dams. Offspring of control mothers (OCM) and diabetic mothers (ODM) were evaluated for weight, glucose tolerance, insulin tolerance, and hematopoiesis defects. The effects of aging were examined in normal and high fat diet (HFD)-fed young (8-week-old) and aged (11-month-old) OCM and ODM rats. Results Young adult ODM males on a normal diet, but not females, displayed improved glucose tolerance due to increased insulin levels. Aged ODM males and females gained more weight than OCM on a HFD and had worse glucose tolerance. Aged ODM males fed a HFD were also neutrophilic. Increases in bone marrow cellularity and myeloid progenitors preceded neutrophilia in ODM males fed a HFD. Conclusion When combined with other risk factors like HFD and aging, changes in glucose metabolism and hematopoiesis may contribute to the increased risk of obesity, type 2 diabetes, and hypertension observed in children of GDM mothers.en_US
dc.eprint.versionAuthor's manuscripten_US
dc.identifier.citationBlue, E. K., Ballman, K., Boyle, F., Oh, E., Kono, T., Quinney, S. K., … Haneline, L. S. (2015). Fetal hyperglycemia and a high fat diet contribute to aberrant glucose tolerance and hematopoiesis in adulthood. Pediatric Research, 77(2), 316–325. http://doi.org/10.1038/pr.2014.185en_US
dc.identifier.issn0031-3998en_US
dc.identifier.urihttps://hdl.handle.net/1805/8769
dc.language.isoen_USen_US
dc.publisherNature Publishing Groupen_US
dc.relation.isversionof10.1038/pr.2014.185en_US
dc.relation.journalPediatric researchen_US
dc.rightsPublisher Policyen_US
dc.sourcePMCen_US
dc.subjectBlood Glucoseen_US
dc.subjectmetabolismen_US
dc.subjectDiabetes Mellitus, Experimentalen_US
dc.subjectComplicationsen_US
dc.subjectDiabetes, Gestationalen_US
dc.subjectFetal Diseasesen_US
dc.subjectHematopoiesisen_US
dc.subjectphysiologyen_US
dc.titleFetal hyperglycemia and a high fat diet contribute to aberrant glucose tolerance and hematopoiesis in adulthooden_US
dc.typeArticleen_US
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