scholarly journals GABA levels in ventral visual cortex decline with age and are associated with neural distinctiveness

2019 ◽  
Author(s):  
Jordan D. Chamberlain ◽  
Holly Gagnon ◽  
Poortata Lalwani ◽  
Kaitlin E. Cassady ◽  
Molly Simmonite ◽  
...  
Keyword(s):  
Older Adults ◽  
Visual Cortex ◽  
Magnetic Resonance ◽  
Aminobutyric Acid ◽  
Resonance Spectroscopy ◽  
Gamma Aminobutyric Acid ◽  
Younger Adults ◽  
Inhibitory Neurotransmitter ◽  
Neural Representations ◽  
Age Related

AbstractAge-related neural dedifferentiation – reduced distinctiveness of neural representations in the aging brain– has been associated with age-related declines in cognitive abilities. But why does neural distinctiveness decline with age? Based on prior work in non-human primates, we hypothesized that the inhibitory neurotransmitter gamma-aminobutyric acid (GABA) declines with age and is associated with neural dedifferentiation. To test this hypothesis, we used magnetic resonance spectroscopy (MRS) to measure GABA and functional MRI (fMRI) to measure neural distinctiveness in the ventral visual cortex in a set of older and younger participants. Relative to younger adults, older adults exhibited lower GABA levels and less distinct activation patterns for faces and houses in the ventral visual cortex. Furthermore, individual differences in GABA within older adults predicted individual differences in neural distinctiveness even after controlling for gray matter volume and age. These results provide novel support for the view that age-related reductions of GABA contribute to age-related reductions in neural distinctiveness (i.e., neural dedifferentiation) in the human ventral visual cortex.Significance StatementNeural representations in the ventral visual cortex are less distinguishable in older compared to younger humans, and this neural dedifferentiation is associated with age-related cognitive deficits. Animal models suggest that reductions in the inhibitory neurotransmitter gamma aminobutyric acid (GABA) may play a role. To investigate this hypothesis, we combined functional magnetic resonance imaging (fMRI) and magnetic resonance spectroscopy (MRS) in a study of the human ventral visual cortex. We observed reduced distinctiveness of neural patterns and reduced GABA levels in older compared to younger adults. Furthermore, older adults with higher GABA levels tended to have more distinctive neural representations. These findings suggest that reduced GABA levels contribute to age-related declines in neural distinctiveness in the human ventral visual cortex.

scholarly journals Neural distinctiveness declines with age in auditory cortex and is associated with auditory GABA levels

2018 ◽  
Author(s):  
Poortata Lalwani ◽  
Holly Gagnon ◽  
Kaitlin Cassady ◽  
Molly Simmonite ◽  
Scott Peltier ◽  
...  
Keyword(s):  
Older Adults ◽  
Visual Cortex ◽  
Individual Differences ◽  
Magnetic Resonance ◽  
Auditory Cortex ◽  
Aging Brain ◽  
Resonance Spectroscopy ◽  
Younger Adults ◽  
Activation Patterns ◽  
Age Related

AbstractNeural activation patterns in the ventral visual cortex in response to different categories of visual stimuli (e.g., faces vs. houses) are less selective, or distinctive, in older adults than in younger adults, a phenomenon known as age-related neural dedifferentiation. Previous work in animals suggests that age-related reductions of the inhibitory neurotransmitter, gamma aminobutyric acid (GABA), may play a role in this age-related decline in neural distinctiveness. In this study, we investigated whether neural dedifferentiation extends to auditory cortex and whether individual differences in GABA are associated with individual differences in neural distinctiveness in humans. 20 healthy young adults (ages 18-29) and 23 healthy older adults (over 65) completed a functional magnetic resonance imaging (fMRI) scan, during which neural activity was estimated while they listened to foreign speech and music. GABA levels in the auditory, ventrovisual and sensorimotor cortex were estimated in the same individuals in a separate magnetic resonance spectroscopy (MRS) scan. Relative to the younger adults, the older adults exhibited both (1) less distinct activation patterns for music vs. speech stimuli and (2) lower GABA levels in the auditory cortex. Also, individual differences in auditory GABA levels (but not ventrovisual or sensorimotor GABA levels) predicted individual differences in neural distinctiveness in the auditory cortex in the older adults. These results demonstrate that age-related neural dedifferentiation extends to the auditory cortex and suggest that declining GABA levels may play a role in neural dedifferentiation in older adults.Significance StatementPrior work has revealed age-related neural dedifferentiation in the visual cortex. GABA levels also decline with age in several parts of the human cortex. Here, we report that these two age-related changes are linked; neural dedifferentiation is associated with lower GABA levels in older adults. We also show that age-related neural dedifferentiation extends to auditory cortex, suggesting that it may be a general feature of the aging brain. These findings provide novel insights into the neurochemical basis of age-related neural dedifferentiation in humans and also offer a potential new avenue for investigating age-related declines in central auditory processing.

scholarly journals Imaging the Pathophysiology of Essential Tremor—A Systematic Review

2021 ◽  
Vol 12 ◽  
Author(s):  
Florian Holtbernd ◽  
N. Jon Shah
Keyword(s):  
Magnetic Resonance ◽  
Essential Tremor ◽  
Neurodegenerative Disorder ◽  
Aminobutyric Acid ◽  
Emission Computed Tomography ◽  
Resonance Spectroscopy ◽  
Gamma Aminobutyric Acid ◽  
Imaging Studies ◽  
Limited Evidence ◽  
Neurotransmitter System

Background: The pathophysiology underlying essential tremor (ET) still is poorly understood. Recent research suggests a pivotal role of the cerebellum in tremor genesis, and an ongoing controversy remains as to whether ET constitutes a neurodegenerative disorder. In addition, mounting evidence indicates that alterations in the gamma-aminobutyric acid neurotransmitter system are involved in ET pathophysiology. Here, we systematically review structural, functional, and metabolic neuroimaging studies and discuss current concepts of ET pathophysiology from an imaging perspective.Methods: We conducted a PubMed and Scopus search from 1966 up to December 2020, entering essential tremor in combination with any of the following search terms and their corresponding abbreviations: positron emission tomography (PET), single-photon emission computed tomography (SPECT), magnetic resonance imaging (MRI), magnetic resonance spectroscopy (MRS), and gamma-aminobutyric acid (GABA).Results: Altered functional connectivity in the cerebellum and cerebello-thalamico-cortical circuitry is a prevalent finding in functional imaging studies. Reports from structural imaging studies are less consistent, and there is no clear evidence for cerebellar neurodegeneration. However, diffusion tensor imaging robustly points toward microstructural cerebellar changes. Radiotracer imaging suggests that the dopaminergic axis is largely preserved in ET. Similarly, measurements of nigral iron content and neuromelanin are unremarkable in most studies; this is in contrast to Parkinson's disease (PD). PET and MRS studies provide limited evidence for cerebellar and thalamic GABAergic dysfunction.Conclusions: There is robust evidence indicating that the cerebellum plays a key role within a multiple oscillator tremor network which underlies tremor genesis. However, whether cerebellar dysfunction relies on a neurodegenerative process remains unclear. Dopaminergic and iron imaging do not suggest a substantial overlap of ET with PD pathophysiology. There is limited evidence for alterations of the GABAergic neurotransmitter system in ET. The clinical, demographical, and genetic heterogeneity of ET translates into neuroimaging and likely explains the various inconsistencies reported.

scholarly journals Edited Magnetic Resonance Spectroscopy Detects an Age-Related Decline in Nonhuman Primate Brain GABA Levels

2016 ◽  
Vol 2016 ◽  
pp. 1-7 ◽  
Author(s):  
Xuanzi He ◽  
Bang-Bon Koo ◽  
Ronald J. Killiany
Keyword(s):  
White Matter ◽  
Gray Matter ◽  
Posterior Cingulate Cortex ◽  
Resonance Spectroscopy ◽  
Gamma Aminobutyric Acid ◽  
Gaba Level ◽  
Inhibitory Neurotransmitter ◽  
Independent Variables ◽  
Age Related ◽  
The Brain

Recent research had shown a correlation between aging and decreasing Gamma-aminobutyric acid (GABA), the primary inhibitory neurotransmitter in the brain. However, how GABA level varies with age in the medial portion of the brain has not yet been studied. The purpose of this study was to investigate the GABA level variation with age focusing on the posterior cingulate cortex, which is the “core hub” of the default mode network. In this study, 14 monkeys between 4 and 21 years were recruited, and MEGA-PRESS MRS was performed to measure GABA levels, in order to explore a potential link between aging and GABA. Our results showed that a correlation between age and GABA+/Creatine ratio was at the edge of significance (r=-0.523,p=0.081). There was also a near-significant trend between gray matter/white matter ratio and the GABA+/Creatine ratio (r=-0.518,p=0.0848). Meanwhile, the correlation between age and grey matter showed no significance (r=-0.028,p=0.93). Therefore, age and gray matter/white matter ratio account for different part ofR-squared (adjustedR-squared = 0.5187) as independent variables for predicting GABA levels. AdjustedR-squared is about 0.5 for two independent variables. These findings suggest that there is internal neurochemical variation of GABA levels in the nonhuman primates associated with normal aging and structural brain decline.

In Vivo Brain Glutathione is Higher in Older Age and Correlates with Mobility

2020 ◽  
Author(s):  
K. E. Hupfeld ◽  
H. W. Hyatt ◽  
P. Alvarez Jerez ◽  
M. Mikkelsen ◽  
C. J. Hass ◽  
...  
Keyword(s):  
Oxidative Stress ◽  
Older Adults ◽  
Motor Performance ◽  
Resonance Spectroscopy ◽  
Younger Adults ◽  
Age Related ◽  
Brain Oxidative Stress ◽  
Brain Antioxidants ◽  
Insight Into

AbstractBrain markers of oxidative damage increase with advancing age. In response, brain antioxidant levels may also increase with age, although this has not been well investigated. Here we used edited magnetic resonance spectroscopy to quantify endogenous levels of glutathione (GSH, one of the most abundant brain antioxidants) in 37 young (mean: 21.8 (2.5) years; 19 F) and 23 older adults (mean: 72.8 (8.9) years; 19 F). Accounting for age-related atrophy, we identified higher frontal and sensorimotor GSH levels for the older compared to the younger adults. For the older adults only, higher sensorimotor (but not frontal) GSH was correlated with poorer balance, gait, and manual dexterity. This suggests a regionally-specific relationship between higher brain oxidative stress levels and motor performance declines with age. We suggest these findings reflect a compensatory upregulation of GSH in response to increasing brain oxidative stress with normal aging. Together, these results provide insight into age differences in brain antioxidant levels and implications for motor function.

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