licochalcone-a and Acute-Kidney-Injury

licochalcone-a has been researched along with Acute-Kidney-Injury* in 1 studies

Other Studies

1 other study(ies) available for licochalcone-a and Acute-Kidney-Injury

ArticleYear
Licochalcone A Attenuates Lipopolysaccharide-Induced Acute Kidney Injury by Inhibiting NF-κB Activation.
    Inflammation, 2016, Volume: 39, Issue:2

    Licochalcone A (Lico A), a flavonoid found in licorice root (Glycyrrhiza glabra), has been reported to have anti-inflammatory activity. However, the protective effects of Lico A on lipopolysaccharide (LPS)-induced acute kidney injury (AKI) remains unclear. In this study, using a mouse model of LPS-induced AKI, we investigated the protective effects and mechanism of Lico A on LPS-induced AKI in mice. LPS-induced kidney injury was assessed by detecting kidney histological study, blood urea nitrogen (BUN), and creatinine levels. The production of inflammatory cytokines TNF-α, IL-6, and IL-1β in serum and kidney tissues was detected by ELISA. The activation of NF-κB was measured by western blot analysis. Our results showed that Lico A dose-dependently attenuated LPS-induced kidney histopathologic changes, serum BUN, and creatinine levels. Lico A also suppressed LPS-induced TNF-α, IL-6, and IL-1β production both in serum and kidney tissues. Furthermore, our results showed that Lico A significantly inhibited LPS-induced NF-κB activation. In conclusion, our results suggest that Lico A has protective effects against LPS-induced AKI and Lico A exhibits its anti-inflammatory effects through inhibiting LPS-induced NF-κB activation.

    Topics: Acute Kidney Injury; Animals; Anti-Inflammatory Agents; Blood Urea Nitrogen; Chalcones; Creatinine; Disease Models, Animal; Enzyme Activation; Fabaceae; Female; Interleukin-1beta; Interleukin-6; Kidney; Lipopolysaccharides; Mice; Mice, Inbred C57BL; NF-kappa B; Plant Preparations; Tumor Necrosis Factor-alpha

2016