کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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5737435 | 1614722 | 2017 | 10 صفحه PDF | دانلود رایگان |
- Age-associated neurochemical concentration differences were measured non-invasively.
- Differences in 8 out of 14 neurochemicals were observed.
- Several differences reflect known region-specific differences in blood flow, metabolism and connectivity.
- Others reveal new aspects of neurochemistry and microstructure associated with oxidative stress and myelination.
- The human brain ages differently depending on region.
The concentrations of fourteen neurochemicals associated with metabolism, neurotransmission, antioxidant capacity, and cellular structure were measured noninvasively from two distinct brain regions using 1H magnetic resonance spectroscopy. Seventeen young adults (age 19-22Â years) and sixteen cognitively normal older adults (age 70-88Â years) were scanned. To increase sensitivity and specificity, 1H magnetic resonance spectra were obtained at the ultra-high field of 7Â T and at ultra-short echo time. The concentrations of neurochemicals were determined using water as an internal reference and accounting for gray matter, white matter, and cerebrospinal fluid content of the volume of interest. In the posterior cingulate cortex (PCC), the concentrations of neurochemicals associated with energy (i.e., creatine plus phosphocreatine), membrane turnover (i.e., choline containing compounds), and gliosis (i.e., myo-inositol) were higher in the older adults while the concentrations of N-acetylaspartylglutamate (NAAG) and phosphorylethanolamine (PE) were lower. In the occipital cortex (OCC), the concentration of N-acetylaspartate (NAA), a marker of neuronal viability, concentrations of the neurotransmitters Glu and NAAG, antioxidant ascorbate (Asc), and PE were lower in the older adults while the concentration of choline containing compounds was higher. Altogether, these findings shed light on how the human brain ages differently depending on region.
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Journal: Neuroscience - Volume 354, 23 June 2017, Pages 168-177