RESUMEN
Acute kidney injury (AKI) is an independent risk factor for the increased risk of death in patients with sepsis. In the current study, we first investigated the expression of circMTO1 in sepsis-induced AKI, and the underlying mechanism was further elucidated. The results showed that circMTO1 expression level was significantly decreased in serums and kidney tissues of US rats and RMCs treated with LPS. Besides, circMTO1 overexpression promoted cell viability, suppressed cell apoptosis and cytokines production of LPS-treated RMCs. Bioinformatics analysis showed that circMTO1 served as a sponge for miR-337. Furthermore, circMTO1 could inhibit the expression of KLF6. Altogether, our study first reported that circMTO1 expression was decreased in sepsis-induced AKI rat models and RMCs treated with LPS. CircMTO1 overexpression could attenuate AKI development by sponging miR-337 and regulating KLF6 expression, which may provide new ideas for evaluation the pathogenesis and the treatment of sepsis-induced AKI.
Asunto(s)
Lesión Renal Aguda/metabolismo , Lesión Renal Aguda/prevención & control , MicroARNs/metabolismo , Proteínas de Unión al ARN/biosíntesis , Lesión Renal Aguda/inducido químicamente , Animales , Supervivencia Celular/efectos de los fármacos , Supervivencia Celular/fisiología , Células Cultivadas , Lipopolisacáridos/toxicidad , Masculino , Ratas , Ratas Sprague-Dawley , Sepsis/inducido químicamente , Sepsis/metabolismo , Sepsis/prevención & controlRESUMEN
There are two independent 3,5-dimethyl-pyrazole and two independent 2-hy-droxy-5-(phenyl-diazen-yl)benzoic acid mol-ecules [in which intra-molecular O-Hâ¯O bonds form S(6) graph-set motifs] in the asymmetric unit of the title compound, C(5)H(8)N(2)·C(13)H(10)N(2)O(3). In the crystal, the components are linked by inter-molecular O-Hâ¯O, O-Hâ¯N and N-Hâ¯O hydrogen bonds, forming four-component clusters. Further stabilization is provided by weak C-Hâ¯π inter-actions.