Open AccessmiR‐485's anti‐drug resistant epilepsy effects by regulating SV2A/PSD‐95 and targeting ABCC1 and neuronal signaling‐transduction proteins in hippocampus of rats
Author(s) -
Wang Kaixuan,
Wu Jing,
Wang Jiangping,
Jiang Kewen
Publication year - 2021
Publication title -
brain and behavior
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.915
H-Index - 41
ISSN - 2162-3279
DOI - 10.1002/brb3.2247
Subject(s) - dentate gyrus , hippocampus , epilepsy , hippocampal formation , neuroscience , biology , signal transduction , pharmacology , microbiology and biotechnology
Aim Drug‐resistant epilepsy (DRE), most subsequently developing refractory epilepsy, causes a significant burden to the society. microRNAs have been demonstrated as key regulators and therapeutic targets in epilepsy. Accordingly, the aim of the present study was to test whether miR‐485 could be a potential target for DRE. Methods and results An in vivo DRE model was developed in Sprague–Dawley rats by lithium chloride‐pilocarpine and screened by antiepileptic drugs. We found that miR‐485‐5p in hippocampus was significant downregulated at early stage and recovered to normal level at late stage of DRE. Overexpression of miR‐485‐5p in dentate gyrus (DG) of hippocampus in DRE rats could significantly decrease the frequency of seizures and the numbers of epileptiform spikes of hippocampal DG neuron, and could specifically decrease SV2A expression without affecting PSD‐95 expression in DG. Furthermore, miR‐485‐5p overexpression could significantly downregulate the expression of efflux transporter related to multidrug resistance (ABCC1) in hippocampus at late stage of DRE. Finally, a specific expression pattern of neuronal signaling‐transduction proteins (LRP4, MDM4, p53, and TMBIM1) for DRE was observed, and miR‐485‐5p overexpression could modulate these proteins’ expression levels toward normal in hippocampus both at early and late stage of DRE. Conclusion Collectively, these results suggest that miR‐485 was a potential target for anti‐DRE, and this effects might be partially via miR‐485‐5p/homeostatic‐synaptic plasticity‐molecule axis and/or targeting efflux transporter (ABCC1) and other neuronal signaling‐transduction proteins (LRP4, MDM4, p53, and TMBIM1).