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Journal: Heliyon
Article Title: Imbalance of glutamatergic and GABAergic neurotransmission in audiogenic seizure-susceptible L eucine-rich glioma-inactivated 1 ( Lgi1 )-mutant rats
doi: 10.1016/j.heliyon.2023.e17984
Figure Lengend Snippet: Schematic overview and experimental flow chart of in vivo microdialysis techniques (A). Glutamate and GABA release in the hippocampus. Extracellular levels of glutamate (B) and GABA (C) were compared between wild-type (WT) rats and Lgi1 -mutant rats. Depolarization stimulation involved applying high-concentration K + (50 mM)-containing artificial cerebrospinal fluid (aCSF) for 60 min through the dialysis probe. Each point represents the mean ± S.E.M. of 5 or 6 animals. * P < 0.05, ** P < 0.01, significantly different from WT group.
Article Snippet:
Techniques: In Vivo, Mutagenesis, Concentration Assay
Journal: Heliyon
Article Title: Imbalance of glutamatergic and GABAergic neurotransmission in audiogenic seizure-susceptible L eucine-rich glioma-inactivated 1 ( Lgi1 )-mutant rats
doi: 10.1016/j.heliyon.2023.e17984
Figure Lengend Snippet: Glutamate release in the hippocampus. Extracellular levels of glutamate were compared between non-primed wild-type (WT) and primed WT rats (A), non-primed Lgi1 -mutant and primed Lgi1 -mutant rats (B), and primed WT and primed Lgi1 -mutant rats (C) (data from B redisplayed for comparisons between non-primed rats and primed rats). Depolarization stimulation involved applying high-concentration K + (50 mM)-containing artificial cerebrospinal fluid (High K + ) for 60 min through the dialysis probe. Each point represents the mean ± S.E.M. of 5–7 animals. * P < 0.05, ** P < 0.01, significantly different from each other group.
Article Snippet:
Techniques: Mutagenesis, Concentration Assay
Journal: Heliyon
Article Title: Imbalance of glutamatergic and GABAergic neurotransmission in audiogenic seizure-susceptible L eucine-rich glioma-inactivated 1 ( Lgi1 )-mutant rats
doi: 10.1016/j.heliyon.2023.e17984
Figure Lengend Snippet: GABA release in the hippocampus. Extracellular levels of GABA were compared between non-primed wild-type (WT) and primed WT rats (A), non-primed Lgi1 -mutant and primed Lgi1 -mutant rats (B), and primed WT and primed Lgi1 -mutant rats (C) (data from C redisplayed for comparisons between non-primed rats and primed rats). Depolarization stimulation involved applying high-concentration K + (50 mM)-containing artificial cerebrospinal fluid (High K + ) for 60 min. Each point represents the mean ± S.E.M. of 5–7 animals. ** P < 0.01, significantly different from each other group.
Article Snippet:
Techniques: Mutagenesis, Concentration Assay
Journal: Heliyon
Article Title: Imbalance of glutamatergic and GABAergic neurotransmission in audiogenic seizure-susceptible L eucine-rich glioma-inactivated 1 ( Lgi1 )-mutant rats
doi: 10.1016/j.heliyon.2023.e17984
Figure Lengend Snippet: Summarized results on hippocampal glutamate and GABA release in Lgi1 -mutant rats (A) and schematic drawing on the imbalance of glutamatergic and GABAergic neurotransmission potentially linked to audiogenic seizure-susceptibility in Lgi1 -mutant rats (B). Under naïve (non-primed) conditions, the Lgi1 -mutation potentiated high K + depolarization-evoked glutamate and GABA release. On the other hand, acoustic priming (AP) stimulation (at P16) increased the basal glutamate level both in Lgi1 -mutant and WT rats. It should be noted that, under primed condition, the Lgi1 -mutation caused enhanced glutamate release and diminished GABA release during high K + depolarization (shown in yellow). This imbalance of glutamatergic and GABAergic neurotransmission in primed Lgi1 -mutant rats may be involved in generation of audiogenic seizures associated with Lgi1 -mutation. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Article Snippet:
Techniques: Mutagenesis