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Oxid Med Cell Longev ; 2020: 1813798, 2020.
Article in English | MEDLINE | ID: mdl-32908623

ABSTRACT

Hemp seed has been used as a traditional oriental medicine and health food in China for centuries. Polysaccharides from hemp seed (HSP) exhibit important properties of intestinal protection, but there are limited data on the specific underlying mechanism. The primary objective of this study was to investigate the protective effect of HSP on intestinal oxidative damage induced by cyclophosphamide (Cy) in mice. The results showed that pretreatment with HSP significantly increased the average daily gain, thymus index, spleen index, superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GSH-Px) activity in serum and ileal homogenate and significantly reduced malondialdehyde (MDA) content in ileal homogenate. In addition, the expression levels of SOD, GSH-Px, Nrf2, heme oxidase-1 (HO-1), and quinoneoxidoreductase-1 (NQO1) mRNA in ileal homogenate were significantly increased. Western blot results showed that HSP significantly upregulated the expression of Nrf2 protein and downregulated the expression of Keap1 protein in the ileum. Collectively, our findings indicated that HSP had protective effects on intestinal oxidative damage induced by Cy in mice, and its mechanism might be related to the activation of Nrf2-Keap1 signaling pathway.


Subject(s)
Cannabis/chemistry , Cyclophosphamide/adverse effects , Kelch-Like ECH-Associated Protein 1/metabolism , NF-E2-Related Factor 2/metabolism , Oxidative Stress/drug effects , Polysaccharides/pharmacology , Seeds/chemistry , Signal Transduction , Animals , Body Weight/drug effects , Catalase/blood , Glutathione Peroxidase/blood , Ileum/metabolism , Inactivation, Metabolic/genetics , Jejunum/drug effects , Jejunum/ultrastructure , Male , Malondialdehyde/metabolism , Mice, Inbred ICR , Monosaccharides/analysis , Organ Specificity/drug effects , Protective Agents/pharmacology , Signal Transduction/drug effects , Spectroscopy, Fourier Transform Infrared , Superoxide Dismutase/blood
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