Mean amplitude of low frequency fluctuations measured by fMRI at 11.7 T in the aging brain of mouse lemur primate

Non-human primates are a critical species for the identification of key biological mechanisms in normal and pathological aging. One of these primates, the mouse lemur, has been widely studied as a model of cerebral aging or Alzheimer's disease. The amplitude of low-frequency fluctuations of blood oxygenation level-dependent (BOLD) can be measured with functional MRI. Within specific frequency bands (e.g. the 0.01-0.1 Hz), these amplitudes were proposed to indirectly reflect neuronal activity as well as glucose metabolism. Here, we first created whole brain maps of the mean amplitude of low frequency fluctuations (mALFF) in young mouse lemurs (mean +/- SD: 2.1 +/- 0.8 years). Then, we extracted mALFF in old lemurs (mean +/- SD: 8.8 +/- 1.1 years) to identify age-related changes. A high level of mALFF was detected in the temporal cortex (Brodmann area 20), somatosensory areas (Brodmann area 5), insula (Brodmann areas 13-6) and the parietal cortex (Brodmann area 7) of healthy young mouse lemurs. Aging was associated with alterations of mALFF in somatosensory areas (Brodmann area 5) and the parietal cortex (Brodmann area 7).

Automated summary

Non-human primates, such as mouse lemurs, play a crucial role in understanding the biological mechanisms of aging. By using functional MRI, researchers measured the amplitude of low-frequency fluctuations (BOLD) to indirectly reflect neural activity and glucose metabolism. The study found that aging led to alterations in the amplitude of low-frequency fluctuations in specific brain regions, including somatosensory areas and the parietal cortex.