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Glucose oscillations, more than constant high glucose, induce p53 activation and a metabolic memory in human endothelial cells

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Schisano, B., Tripathi, Gyanendra, McGee, K. C., McTernan, P. G. and Ceriello, Antonio (2011) Glucose oscillations, more than constant high glucose, induce p53 activation and a metabolic memory in human endothelial cells. Diabetologia, Vol.54 (No.5). pp. 1219-1226. doi:10.1007/s00125-011-2049-0

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Official URL: http://dx.doi.org/10.1007/s00125-011-2049-0

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Abstract

Aims/hypothesis
Damage persists in HUVECs exposed to a constant high glucose concentration long after glucose normalisation, a phenomenon termed ‘metabolic memory’. Evaluation of the effects of exposure of HUVECs to oscillating high glucose on the induction of markers of oxidative stress and DNA damage (phospho-γ-histone H2AX and PKCδ) and onset of metabolic memory, and the possible role of the tumour suppressor transcriptional factor p53 is of pivotal interest.
Methods
HUVECs were incubated for 3 weeks in 5 or 25 mmol/l glucose or oscillating glucose (24 h in 5 mmol/l glucose followed by 24 h in 25 mmol/l glucose) or for 1 week in constant 5 mmol/l glucose after being exposed for 2 weeks to continuous 25 mmol/l high glucose or oscillating glucose. Transcriptional activity of p53 was also evaluated in the first 24 h after high glucose exposure.
Results
High constant glucose upregulated phospho-γ-histone H2AX and protein kinase C (PKC)δ compared with control. Oscillating glucose was even more effective than both normal and constant high glucose. Both constant and oscillating glucose resulted in a memory effect, which was more pronounced in the oscillating condition. Transcriptional activity of p53 peaked 6 h after glucose exposure, showing a predicted oscillatory behaviour.
Conclusions/interpretation
Exposure to oscillating glucose was more deleterious than constant high glucose and induced a metabolic memory after glucose normalisation. Hyperactivation of p53 during glucose oscillation might be due to the absence of consistent feedback inhibition during each glucose spike and might account for the worse outcome of this condition.

Item Type: Journal Article
Subjects: R Medicine > R Medicine (General)
Divisions: Faculty of Medicine > Warwick Medical School > Biomedical Sciences > Translational & Experimental Medicine > Metabolic and Vascular Health (- until July 2016)
Faculty of Medicine > Warwick Medical School
Journal or Publication Title: Diabetologia
Publisher: Springer
ISSN: 0012-186X
Official Date: May 2011
Dates:
DateEvent
May 2011Published
Volume: Vol.54
Number: No.5
Page Range: pp. 1219-1226
DOI: 10.1007/s00125-011-2049-0
Status: Peer Reviewed
Publication Status: Published
Funder: Novo Nordisk , Research Councils UK (RCUK)

Data sourced from Thomson Reuters' Web of Knowledge

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