4.6 Article

Anti-Oxidant and Anti-Inflammatory Effects of Lipopolysaccharide from Rhodobacter sphaeroides against Ethanol-Induced Liver and Kidney Toxicity in Experimental Rats

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MOLECULES
卷 26, 期 24, 页码 -

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MDPI
DOI: 10.3390/molecules26247437

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alcoholic liver disease; hepcidin; kidney injury molecule-1; lipopolysaccharide from Rhodobacter sphaeroides; nuclear factor kappa B; toll-like receptor 4

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This study demonstrates the protective effects of lipopolysaccharide from Rhodobacter sphaeroides (LPS-RS) against ethanol-induced hepatotoxicity and nephrotoxicity in experimental rats. LPS-RS alleviated oxidative stress, inflammation, and preserved iron homeostasis in the liver and kidney of the rats.
This study aimed to investigate the protective effects of lipopolysaccharide from Rhodobacter sphaeroides (LPS-RS) against ethanol-induced hepatotoxicity and nephrotoxicity in experimental rats. The study involved an intact control group, LPS-RS group, two groups were given ethanol (3 and 5 g/kg/day) for 28 days, and two other groups (LPS-RS + 3 g/kg ethanol) and (LPS-RS + 5 g/kg ethanol) received a daily dose of LPS-RS (800 mu g/kg) before ethanol. Ethanol significantly increased the expression of nuclear factor kappa B (NF-kappa B) and levels of malondialdehyde (MDA), tumor necrosis factor-alpha (TNF-alpha) and interleukin-6 (IL-6) in the liver tissue and decreased anti-oxidant enzymes. Hepcidin expression was downregulated in the liver, with increased serum levels of ferritin and iron. Prior-administration of LPS-RS alleviated the increase in oxidative stress and inflammatory markers, and preserved iron homeostasis markers. In the kidney, administration of ethanol caused significant increase in the expression of NF-kappa B and the levels of TNF-alpha and kidney injury markers; whereas LPS-RS + ethanol groups had significantly lower levels of those parameters. In conclusion; this study reports anti-oxidant, anti-inflammatory and iron homeostasis regulatory effects of the toll-like receptor 4 (TLR4) antagonist LPS-RS against ethanol induced toxicity in both the liver and the kidney of experimental rats.

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