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An Acad Bras Cienc ; 95(suppl 1): e20220750, 2023.
Article in English | MEDLINE | ID: mdl-37466537

ABSTRACT

Sleep deprivation (SD) can lead to cognitive impairment caused by neuroinflammation. MiR-181c-5p/HMGB1 axis plays a part in anti-inflammation effects. However, the mechanism that miR-181c-5p facilitates learning and memory in SD mice remains unclear. So we investigated the role of miR-181c-5p in learning and memory impairment induced by SD. We overexpressed miR-181c-5p in the mice hippocampus by injecting lentivirus vector-miR-181c-5p (LV-miR-181c-5p) particles. Mice were divided into four groups: control (Ctrl), SD, SD + miR-181c-5p and SD + vector. We found that mice in the third group showed ameliorated learning and memory compared with the fourth group. The content of ionized calcium binding adaptor molecule 1 (IBA-1) in the third group was decreased compared with the fourth group. Moreover, the expression levels of HMGB1, TLR4 and p-NF-κB in the hippocampus of overexpressed miR-181c-5p mice were reduced. In total, miR-181c-5p ameliorated learning and memory in SD mice via the HMGB1/TLR4/NF-κB pathway.


Subject(s)
HMGB1 Protein , MicroRNAs , Mice , Animals , NF-kappa B/metabolism , MicroRNAs/genetics , MicroRNAs/metabolism , Toll-Like Receptor 4/genetics , Toll-Like Receptor 4/metabolism , HMGB1 Protein/genetics , HMGB1 Protein/metabolism , Sleep
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