Nrf2-Mediated Neuroprotection Against Recurrent Hypoglycemia Is Insufficient to Prevent Cognitive Impairment in a Rodent Model of Type 1 Diabetes

• DOI: 10.2337/db15-1653
• Publication Date: 2016-07-14T06:35:00Z
• Authors: Alison D. McNeilly; Jennifer R. Galla...; Albena T. Dinkova...; John D. Hayes; John Sharkey; Michael L.J. Ashford; Rory J. McCrimmon
• Keywords: Inflammation; Male; Mice, Knockout; NF-E2-Related Factor 2; 610; Hippocampus; Polymerase Chain Reaction; Hypoglycemia; Mice, Inbred C57BL; Mice; Oxidative Stress; Random Allocation; Diabetes Mellitus, Type 1; 616; Animals; Cognitive Dysfunction; Lipid Peroxidation

It remains uncertain whether recurrent nonsevere hypoglycemia (Hypo) results in long-term cognitive impairment in type 1 diabetes (T1D). This study tested the hypothesis that specifically in the T1D state, Hypo leads to cognitive impairment via a pathological response to oxidative stress. Wild-type (Control) and nuclear factor–erythroid 2 p45–related factor 2 (Nrf2) null mice were studied. Eight groups of mice (Control and Nrf2−/− ± T1D and ± Hypo) were subject to recurrent, twice-weekly, insulin or saline injections over 4 weeks, after which cognitive function was assessed and brain tissue analyzed. Recurrent moderate hypoglycemia in T1D, but not Control, mice significantly impaired cognitive performance, and this was associated with hippocampal oxidative damage and inflammation despite an enhanced expression of Nrf2 and its target genes Hmox1 and Nqo1. In Nrf2−/− mice, both T1D and Hypo independently resulted in impaired cognitive performance, and this was associated with oxidative cell damage and marked inflammation. Together, these data suggest that Hypo induces an Nrf2-dependent antioxidant response in the hippocampus, which counteracts oxidative damage. However, in T1D, this neuroprotective mechanism is insufficient to prevent neuronal oxidative damage, resulting in chronic deficits in working and long-term memory.