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Lipids Health Dis ; 11: 93, 2012 Jul 23.
Article in English | MEDLINE | ID: mdl-22824368

ABSTRACT

BACKGROUND: This study aimed at investigating the oxidative stress ameliorating effect, lipids profile restoration, and the anti-inflammatory effect of Samsum Ant Venom (SAV) in induced endotoxemic male rats, injected with bacterial lipopolysaccharides (LPS). RESULTS: Results revealed that LPS significantly increased the oxidative stress indications in LPS-injected rats. A significant increase of both malondialdehyde (MDA), and advanced oxidative protein products (AOPP), as well as a significant suppression of glutathione were all detected. Treatment with 100 µg/kg dose of SAV significantly restored the oxidative stress normal indications and increased the total glutathione levels. Treatment of the LPS-rats with 100 µg/kg dose of SAV showed a clear anti-inflammatory function; as the histological architecture of the hepatic tissue was partially recovered, along with a valuable decrease in the leukocytes infiltrated the hepatic tissues. Treatment of some rat groups with 600 µg/kg dose of SAV after LPS injection induced a severe endotoxemia that resulted in very high mortality rates. SAV versus the effects of LPS on AKT1, Fas, TNF-α and IFN-γ mRNA expression. SAV was found to significantly lower Fas gene expression comparing to the LPS group and restore the level of IFN-γ mRNA expression to that of the control group. CONCLUSION: In conclusion, SAV, at the dose of 100 µg/kg body weight, maintained and restored the oxidative stability, the anti-inflammatory, and the hypolipidemic bioactivity in rats after induced disruption of these parameters by LPS injection. This improvement by SAV was mediated by upregulation of AKT1.


Subject(s)
Anti-Inflammatory Agents/therapeutic use , Antioxidants/metabolism , Ants/chemistry , Lipopolysaccharides/pharmacology , Proto-Oncogene Proteins c-akt/metabolism , Venoms/therapeutic use , Animals , Endotoxemia/chemically induced , Endotoxemia/drug therapy , Glutathione/metabolism , Interferon-gamma/metabolism , Malondialdehyde/metabolism , Oxidative Stress/drug effects , Rats , Tumor Necrosis Factor-alpha/metabolism
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