Altered Brain Mitochondrial Metabolism in Healthy Aging as Assessed by in vivo Magnetic Resonance Spectroscopy

Author:

Boumezbeur Fawzi12,Mason Graeme F13,de Graaf Robin A14,Behar Kevin L13,Cline Gary W5,Shulman Gerald I567,Rothman Douglas L14,Petersen Kitt F5

Affiliation:

1. Department of Diagnostic Radiology, Yale School of Medicine, New Haven, Connecticut, USA

2. Neurospin, I2BM, CEA, Gif-sur-Yvette, France

3. Department of Psychiatry, Yale School of Medicine, New Haven, Connecticut, USA

4. Department of Biomedical Engineering, Yale School of Medicine, New Haven, Connecticut, USA

5. Department of Internal Medicine, Yale School of Medicine, New Haven, Connecticut, USA

6. Department of Cellular and Molecular Physiology, Yale School of Medicine, New Haven, Connecticut, USA

7. Howard Hughes Medical Institute, Yale School of Medicine, New Haven, Connecticut, USA

Abstract

A decline in brain function is a characteristic feature of healthy aging; however, little is known about the biologic basis of this phenomenon. To determine whether there are alterations in brain mitochondrial metabolism associated with healthy aging, we combined 13C/1H magnetic resonance spectroscopy with infusions of [1-13C]glucose and [2-13C]acetate to quantitatively characterize rates of neuronal and astroglial tricarboxylic acid cycles, as well as neuroglial glutamate–glutamine cycling, in healthy elderly and young volunteers. Compared with young subjects, neuronal mitochondrial metabolism and glutamate–glutamine cycle flux was ∼30% lower in elderly subjects. The reduction in individual subjects correlated strongly with reductions in N-acetylaspartate and glutamate concentrations consistent with chronic reductions in brain mitochondrial function. In elderly subjects infused with [2-13C]acetate labeling of glutamine, C4 and C3 differed from that of the young subjects, indicating age-related changes in glial mitochondrial metabolism. Taken together, these studies show that healthy aging is associated with reduced neuronal mitochondrial metabolism and altered glial mitochondrial metabolism, which may in part be responsible for declines in brain function.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Neurology (clinical),Neurology

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