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Eur Rev Med Pharmacol Sci ; 23(17): 7184-7190, 2019 Sep.
Article in English | MEDLINE | ID: mdl-31539104

ABSTRACT

OBJECTIVE: To evaluate the effect of interleukin-19 (IL-19) treatment on epidural fibrosis and its mechanism of action with transforming growth factor ß (TGF-ß). MATERIALS AND METHODS: Initially, IL-19 (10, 20, 50 and 100 ng/L) was used to pretreat rat fibroblasts. TGF-ß (10 µg/L) was then applied to activate fibroblasts. The protein expression levels of TGF-ß receptor, extracellular-signal-regulated kinase (Erk) and p-38 were measured by Western blotting. In addition, we performed laminectomy at T10 vertebral plate in rats, followed by injection of IL-19 in caudal vein one week after injury. Furthermore, IL-19, TGF-ß and fibrosis indexes were measured by quantitative Real-time polymerase chain reaction (qRT-PCR) and Western blotting at 7 and 28 days after injury, respectively. RESULTS: Concentration-dependent IL-19 significantly down-regulated TGF-ß receptor expression and inhibited phosphorylated Erk (p-Erk) and phosphorylated p38 (p-p38). In vivo, IL-19 reduced the expressions of TGF-ß and connective tissue growth factor (CTGF) at 7 days. Furthermore, IL-19 significantly suppressed extracellular matrix productions formation, including α smooth muscle actin (α-SMA) and collagen-1 (COL-1), and fibronectin at 28 days. CONCLUSIONS: IL-19 inhibited TGF-ß expression via Erk and p38 pathway. Moreover, it decreased CTGF expression to suppress α-SMA, COL-1 and fibronectin in scar tissues, thereby preventing spinal cord from compression of scar tissues.


Subject(s)
Cicatrix/drug therapy , Epidural Space/pathology , Fibroblasts/cytology , Interleukins/administration & dosage , MAP Kinase Signaling System/drug effects , Transforming Growth Factor beta/metabolism , Animals , Cells, Cultured , Cicatrix/pathology , Disease Models, Animal , Down-Regulation , Epidural Space/drug effects , Extracellular Signal-Regulated MAP Kinases/metabolism , Fibroblasts/drug effects , Fibrosis , Gene Expression Regulation/drug effects , Interleukins/pharmacology , Primary Cell Culture , Rats , Transforming Growth Factor beta/pharmacology , Treatment Outcome
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