Time course of the effect of status epilepticus induced in the developing rat on γ-amino butyric acid and glutamate cerebellar concentration

• Published in: Neurologia (Barcelona, Spain) Vol. 33; no. 9; p. 577
• Main Authors: Hernández-Martínez, D, Rocha, L, Martínez-Quiroz, J, Morgado-Valle, C, Manzo, J, López-Meraz, M L
• Format: Journal Article
• Language: English
• Published: Spain 01.11.2018
• Subjects: Animals; Cerebellum - drug effects; Cerebellum - metabolism; gamma-Aminobutyric Acid - metabolism; Glutamic Acid - metabolism; Growth and Development; Male; Rats; Rats, Wistar; Status Epilepticus - chemically induced; Status Epilepticus - metabolism; Cerebellum; Cerebelo; Glutamato; Ácido γ-aminobutírico; Glutamate; Status epilepticus; γ-amino butyric acid
• ISSN: 1578-1968
• DOI: 10.1016/j.nrl.2016.07.010

Status epilepticus (SE) is an epileptic condition that can cause cerebellar atrophy and loss of Purkinje cells in both humans and research animals. Cerebellum is a region rich in γ-aminobutyric acid (GABA) and glutamate, and some studies have shown that their concentrations may be altered after convulsions. However, there are no studies showing the effect of seizures on different cerebellar regions in developing rats. Time course of the effect of status epilepticus induced in the developing rat on γ-amino butyric acid and glutamate cerebellar concentration. SE was induced using the lithium-pilocarpine model; control rats were injected with saline solution. At 6h, 24h, and 1 month after SE o saline injection, rats were anaesthetised with pentobarbital and decapitated, and cerebella were extracted. The vermis and hemispheres were dissected and homogenised in 0.1M perchloric acid containing 4mM sodium bisulfite. Homogenates were centrifuged and supernatant was used to quantify GABA, and glutamate tissue concentrations by HPLC coupled with fluorometric detection. SE did not alter GABA and glutamate tissue concentration in the cerebellar vermis and hemispheres. The developing rat cerebellum is resistant to both short- and long-term neurochemical changes induced by SE.