Increased Cyclic Adenosine Monophosphate Responsive Element is Closely Associated with the Pathogenesis of Drug-resistant Epilepsy

• Published in: Current neurovascular research Vol. 21; no. 1; p. 54
• Main Authors: Li, Jing-Xuan, Shi, Dai, Ren, Si-Ying, Wu, Guo-Feng
• Format: Journal Article
• Language: English
• Published: United Arab Emirates 01.01.2024
• Subjects: Animals; Anticonvulsants - pharmacology; Anticonvulsants - therapeutic use; Cyclic AMP Response Element-Binding Protein - metabolism; Disease Models, Animal; Drug Resistant Epilepsy - metabolism; Hippocampus - drug effects; Hippocampus - metabolism; Male; Phenobarbital - pharmacology; Pilocarpine - toxicity; Rats; Rats, Sprague-Dawley; Receptors, GABA-A - biosynthesis; Receptors, GABA-A - metabolism; drug-resistant epilepsy; status epilepticus; CREB; GABA A receptor; Epilepsy; γ-aminobutyric
• ISSN: 1875-5739
• DOI: 10.2174/0115672026290996240307072539

Drug-resistant epilepsy (DRE) is a refractory neurological disorder. There is ample evidence that suggest that γ-aminobutyric acid-a (GABAA) receptors could be one of the mechanisms responsible for the development of drug resistance in epilepsy. It is also known that the cAMP response element binding protein (CREB) plays a possible key role in the transcriptional regulation of GABA . This study explores the role of CREB in the development of DRE and the effect of CREB on GABA-related receptors in DRE. The CREB expression was increased or decreased in the hippocampus of normal rats by lentiviral transfection, who then underwent the lithium-pilocarpine-induced epilepsy model. Phenobarbital (PB) sodium and carbamazepine (CBZ) were used to select a drug-resistant epileptic model. The expression levels of GABA receptor α1, β2, and γ2 subunits and CREB protein were measured in the rat hippocampus by western blot and fluorescent quantitative PCR. The frequency and duration of seizures increased in the overexpression group compared to that in the control group. In addition, the severity, frequency, and duration of seizures decreased in the group with decreased expression. The hippocampus analysis of the expression levels of the CREB protein and CREB mRNA yielded similar findings. Altering the CREB protein expression in the rat hippocampus could negatively regulate the expression and transcript levels of GABA receptors α1, β2, and γ2, suggesting that CREB may serve as a potential target for the development of treatment protocols and drugs for epilepsy. Our study shows that enhanced CREB expression promotes the development of DRE and negatively regulates GABA receptor levels and that the inhibition of CREB expression may reduce the incidence of DRE.