Global metabolic reprogramming and sex-specific impact of caloric restriction in a mouse model of Alzheimer’s disease
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Background
Alzheimer’s disease (AD), disproportionally affecting women, is generally regarded as a disease of the brain. Yet, cumulative evidence increasingly supports a more systemic, full-body view on this incurable disorder, with the liver and kidneys playing an important role in amyloid clearance. The latter is likely potentiated by caloric restriction (CR), but its impact on the metabolism of key amyloid-handling tissues is poorly understood.
Methods
We examined the sex-specific effects of amyloidosis and CR on oxidative and metabolic processes in APPPS1 mice, expressing mutant amyloidogenic proteins under the neuronal Thy-1 promoter. Wild-type (WT) and APPPS1 mice were either fed ad libitum (AL) or received 70% of their individual AL intake (CR regimen).
Results
Compared to age-matched WT controls, the brain, liver, and kidney of 9-month-old AL APPPS1 mice exhibited higher levels of oxidative stress markers along with altered activity of antioxidant enzymes, including higher superoxide dismutase and lower catalase activity. These differences were sex- and tissue-specific, with kidneys showing the largest AD-induced differences between sexes. As for key glycolytic enzymes, APPPS1 mice possessed higher activity of pyruvate kinase than WT mice in all organs and higher hexokinase and phosphofructokinase activities in the brain, with stronger effects observed in males. CR intensified oxidative stress in the liver and the female brain but reduced it in the female kidney. Moreover, it potentiated glycolysis predominantly in females and modulated glutathione-dependent enzymes in a sex-dependent manner.
Conclusions
Neuron-driven amyloidosis induces strong and significant metabolic changes in the entire body, encompassing ubiquitous oxidative damage, enhancement of glycolysis, and antioxidant defense. The lower activity of glycolytic enzymes in the female brain and decreased antioxidant defense in the female liver and kidney provide yet another facet to the complex picture of female vulnerability in AD. Females seemed to profit more from CR, but the general CR effect was not very strong.
