[HTML][HTML] Gut neurotoxin p-cresol induces differential expression of GLUN2B and GLUN2A subunits of the NMDA receptor in the hippocampus and nucleus accumbens …

G Tevzadze, E Zhuravliova, T Barbakadze… - AIMS …, 2020 - ncbi.nlm.nih.gov
G Tevzadze, E Zhuravliova, T Barbakadze, L Shanshiashvili, D Dzneladze, Z Nanobashvili…
AIMS neuroscience, 2020ncbi.nlm.nih.gov
Mislocalization and abnormal expression of N-methyl-D-aspartate glutamate receptor
(NMDAR) subunits is observed in several brain disorders and pathological conditions.
Recently, we have shown that intraperitoneal injection of the gut neurotoxin p-cresol induces
autism-like behavior and accelerates seizure reactions in healthy and epilepsy-prone rats,
respectively. In this study, we evaluated the expression of GLUN2B and GLUN2A NMDAR
subunits, and assessed the activity of cAMP-response element binding protein (CREB) and …
Abstract
Mislocalization and abnormal expression of N-methyl-D-aspartate glutamate receptor (NMDAR) subunits is observed in several brain disorders and pathological conditions. Recently, we have shown that intraperitoneal injection of the gut neurotoxin p-cresol induces autism-like behavior and accelerates seizure reactions in healthy and epilepsy-prone rats, respectively. In this study, we evaluated the expression of GLUN2B and GLUN2A NMDAR subunits, and assessed the activity of cAMP-response element binding protein (CREB) and Rac1 in the hippocampi and nucleus accumbens of healthy and epilepsy-prone rats following p-cresol administration. We have found that subchronic intraperitoneal injection of p-cresol induced differential expression of GLUN2B and GLUN2A between the two brain regions, and altered the GLUN2B/GLUN2A ratio, in rats in both groups. Moreover, p-cresol impaired CREB phosphorylation in both brain structures and stimulated Rac activity in the hippocampus. These data indicate that p-cresol differently modulates the expression of NMDAR subunits in the nucleus accumbens and hippocampi of healthy and epilepsy-prone rats. We propose that these differences are due to the specificity of interactions between dopaminergic and glutamatergic pathways in these structures.
ncbi.nlm.nih.gov
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