Blunted cardiac AMPK response is associated with susceptibility to ischemia/ reperfusion in Male offspring of gestational diabetic rats

Xiaofang Luo, Hong Zou, Ping Xu, Li Wen, Joanna L. Stanley, Xiaoxue Jiang, Ting-li Han, David Olson, Chuan Peng, Chen Zhang, Xiaoqiu Xiao, Chao Tong, Hongbo Qi, Philip N. Baker

Research output: Contribution to journalArticlepeer-review

Abstract

Background/Aims: Gestational diabetes mellitus (GDM) is closely associated with early perinatal complications and long-term health problems, such as cardiovascular disease, in offspring. AMP-activated protein kinase (AMPK) is cardioprotective, particularly in the treatment of ischemia/reperfusion (I/R). However, whether GDM programs offspring susceptibility to cardiac I/R and the involvement of AMPK remain unclear. Methods: Streptozotocin was administered to rats during mid pregnancy; the postpartum maternal metabolome was assessed by chromatography-mass spectrometry (GC-MS). Male offspring were subjected to body composition scanning followed by ex vivo global I/R. Cardiac signaling was determined by Western blotting. Results: The body weights (BWs) of the GDM male offspring were significantly heavier than those of the control group from the age of 8 weeks; the heart weights (HWs) and HW/BW were also increased in the GDM group compared to the control group. The ex vivo post-I/R cardiac contractile function recovery was significantly compromised in the GDM male offspring. The phosphorylation of AMPK and ACC was elevated by ex vivo I/R in both groups, but to a significantly lesser extent in the GDM group. Conclusion: GDM male offspring rats have higher risks of overgrowth and intolerance to cardiac I/R, which may be due to a compromised AMPK signaling pathway.

Original languageEnglish
Pages (from-to)1103-1116
Number of pages14
JournalCellular Physiology and Biochemistry
Volume52
Issue number5
DOIs
Publication statusPublished - 13 Apr 2019

Keywords

  • AMPK
  • Cardiac function
  • Fetal programming
  • Gestational diabetes mellitus
  • Ischemia/reperfusion

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