Twelve rats were randomly divided into four groups: sham group and SCI group (1 day, 2 days, and 3 days after SCI) (n = 3 per group). The parenchymal tissue at the surgery site was extracted for western blotting and qRT-PCR analysis, as previously described. The remaining 48 rats were randomly divided into the following four groups, and testing was performed by blinded observers: (1) sham group (the rats were subjected to sham operation), (2) control group (the rats were subjected to SCI and were treated with PBS), (3) agomir-NC group (the rats were subjected to SCI and treated with agomir-NC [RiboBio, Guangzhou, China]), and (4) agomir-135a-5p group (the rats were subjected to SCI and treated with 25 μL of 10 nmol agomir-135a-5p [RiboBio, Guangzhou, China]) (n = 12 per group). The damaged spinal cords were collected 7 days after intrathecal injection for further western blotting and immunofluorescence analyses.
+ Open protocol