کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5738789 1615055 2017 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Research articleGlutamatergic metabolites are associated with visual plasticity in humans
ترجمه فارسی عنوان
مقاله پژوهشی متابولیت های گلوتاماترگیک با پلاستیک های بصری در انسان ارتباط دارد
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی علوم اعصاب (عمومی)
چکیده انگلیسی


- First study of visual plasticity using multi-modal neuroimaging in humans.
- Used a fMRI paradigm with high frequency stimulation to study visual plasticity.
- Used MRS to measure glutamate (Glu), glutamine (Gln), and GABA.
- LTP-like visual plasticity was observed, similar to past animal and human studies.
- Resting visual cortical Glu, Gln, and GABA predict visual plasticity in humans.

Long-term potentiation (LTP) is a basic cellular mechanism underlying learning and memory. LTP-like plasticity in the visual cortex can be induced by high frequency visual stimulation in rodents and humans. Since glutamate plays a fundamental role in LTP, this study investigated if visual cortical glutamate and glutamine levels, measured by proton magnetic resonance spectroscopy (MRS), relate to visual plasticity in humans. Since plasticity requires a delicate excitation and inhibition balance, GABA was also explored. Eighteen healthy participants completed MRS and a visual fMRI paradigm. Results revealed enhanced fMRI activations after high frequency visual stimulation, suggesting visual plasticity occurred. Higher activations were associated with higher resting glutamine levels after family wise error-correction. Exploratory analyses revealed that higher resting glutamate and GABA levels were associated with visual plasticity, suggesting there may be a critical excitation-inhibition balance necessary for experience dependent plasticity. This is the first empirical evidence that resting glutamine levels and potentially glutamate and GABA levels are associated with visual plasticity in humans.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Neuroscience Letters - Volume 644, 22 March 2017, Pages 30-36
نویسندگان
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