Sex specific correlation between GABAergic disruption in the dorsal hippocampus and flurothyl seizure susceptibility after neonatal hypoxic-ischemic brain injury
Autor: | Ryan J. Felling, Carl E. Stafstrom, Melanie A. McNally, Charles R. Lechner, Raul Chavez-Valdez, Mark St. Pierre, Frances J. Northington |
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Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
0301 basic medicine
medicine.medical_specialty Convulsants Hippocampal formation Hippocampus Article Sex-dimorphism lcsh:RC321-571 03 medical and health sciences Mice 0302 clinical medicine Sex Factors GABA receptor Interneurons Seizures Internal medicine Flurothyl medicine Animals GABAergic Neurons Neonatal seizure lcsh:Neurosciences. Biological psychiatry. Neuropsychiatry Parvalbumin Hypoxic-ischemic brain injury biology GABAA receptor business.industry Neonatal brain injury 030104 developmental biology Endocrinology Parvalbumins Neurology Animals Newborn Hypoxia-Ischemia Brain biology.protein GABAergic Disease Susceptibility Calretinin business Somatostatin 030217 neurology & neurosurgery |
Zdroj: | Neurobiology of disease Neurobiology of Disease, Vol 148, Iss, Pp 105222-(2021) |
ISSN: | 1095-953X 0969-9961 |
Popis: | Since neonatal hypoxia-ischemia (HI) disrupts the hippocampal (Hp) GABAergic network in the mouse and Hp injury in this model correlates with flurothyl seizure susceptibility only in male mice, we hypothesized that GABAergic disruption correlates with flurothyl seizure susceptibility in a sex-specific manner. C57BL6 mice were exposed to HI (Vannucci model) versus sham procedures at P10, randomized to normothermia (NT) or therapeutic hypothermia (TH), and subsequently underwent flurothyl seizure testing at P18. Only in male mice, Hp atrophy correlated with seizure susceptibility. The number of Hp parvalbumin positive interneurons (PV+INs) decreased after HI in both sexes, but TH attenuated this deficit only in females. In males only, seizure susceptibility directly correlated with the number of PV+INs, but not somatostatin or calretinin expressing INs. Hp GABAB receptor subunit levels were decreased after HI, but unrelated to later seizure susceptibility. In contrast, Hp GABAA receptor α1 subunit (GABAARα1) levels were increased after HI. Adjusting the number of PV+ INs for their GABAARα1 expression strengthened the correlation with seizure susceptibility in male mice. Thus, we identified a novel Hp sex-specific GABA-mediated mechanism of compensation after HI that correlates with flurothyl seizure susceptibility warranting further study to better understand potential clinical translation. |
Databáze: | OpenAIRE |
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