4.8 Article

Gestational diabetes exacerbates maternal immune activation effects in the developing brain

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MOLECULAR PSYCHIATRY
卷 23, 期 9, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/mp.2017.191

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资金

  1. ADA [1-16-IBS-100]
  2. JDRF [1-INO-2014-177-A-V]
  3. Pilot & Feasibility Program of the Vanderbilt Diabetes Research and Training Center
  4. [R01MH079299]
  5. [T32MH064913]
  6. [T32GM007347]
  7. [F31DK108652]
  8. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [F31DK108652] Funding Source: NIH RePORTER
  9. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [T32GM007347] Funding Source: NIH RePORTER
  10. NATIONAL INSTITUTE OF MENTAL HEALTH [R01MH067234, T32MH064913] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Maternal inflammation and diabetes increase the risk for psychiatric disorders in offspring. We hypothesized that these co-occurring risk factors may potentiate each other. To test this, we maternally exposed developing mice in utero to gestational diabetes mellitus (GDM) and/or maternal immune activation (MIA). Fetal mouse brains were exposed to either vehicle, GDM, MIA or GDM+ MIA. At gestational day (GD) 12.5, GDM produced a hyperglycemic, hyperleptinemic maternal state, whereas MIA produced significant increases in proinflammatory cytokines and chemokines. Each condition alone resulted in an altered, inflammatory and neurodevelopmental transcriptome profile. In addition, GDM+MIA heightened the maternal inflammatory state and gave rise to a new, specific transcriptional response. This exacerbated response was associated with pathways implicated in psychiatric disorders, including dopamine neuron differentiation and innate immune response. Based on these data, we hypothesize that children born to GDM mothers and exposed to midgestation infections have an increased vulnerability to psychiatric disorder later in life, and this should be tested in follow-up epidemiological studies.

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