| Literature DB >> 35088373 |
Suresh L Mehta1, Anil K Chokkalla1,2, Saivenkateshkomal Bathula1, Raghu Vemuganti3,4,5.
Abstract
Transient focal ischemia induces a sustained downregulation of miR-7 leading to derepression of its target α-synuclein (α-Syn), which promotes neuronal death. We previously showed that treatment with miR-7 mimic prevents α-Syn induction and protects brain after stroke in rodents irrespective of age and sex. To further decipher the role of miR-7, we currently studied infarction and motor function in miR-7 double knockout mice (lack both miR-7a and miR-7b) subjected to focal ischemia. Adult miR-7-/- mice showed similar motor and cognitive functions to miR-7+/+ mice. However, when subjected to even a mild focal ischemia, the miR-7-/- mice showed exacerbated brain damage and worsened motor function compared with the miR-7+/+ mice. Replenishing miR-7 in miR-7-/- mice (IV injection of miR-7 mimic) restored miR-7 mediated neuroprotection and motor recovery, potentially by preventing α-Syn protein induction. Thus, we show that miR-7 is an essential miRNA in the brain that prevents α-Syn translation and the ensuing brain damage after stroke.Entities:
Keywords: Brain damage; Ischemia; Motor function; Noncoding RNA; Poststroke recovery
Year: 2022 PMID: 35088373 PMCID: PMC9329483 DOI: 10.1007/s12975-021-00981-7
Source DB: PubMed Journal: Transl Stroke Res ISSN: 1868-4483 Impact factor: 6.800