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首页> 外文期刊>Journal of materials science >Protective effect of bioactive ceramics on liver injury:regulation of pro-inflammatory cytokins expression
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Protective effect of bioactive ceramics on liver injury:regulation of pro-inflammatory cytokins expression

机译:生物活性陶瓷对肝损伤的保护作用:调节促炎细胞因子的表达

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Aim of study A bioactive ceramics has been reported to regulate the expression of inflammatory cyto-kines in macrophage cells activated by lipopolysaccharides (LPS). In present study, we investigated the anti-inflammatory effect of bioactive ceramics using liver injury model in mouse. Materials and Methods Mice were divided into three groups: Normal group, LPS group (LPS and no ceramics treatment), Ceramics group (LPS and ceramics treatment). Results LPS administration induced the increase of plasma aspartate aminotransferase (AST) and alanine aminotransferase (ALT) in mouse. The losses of cytoplasm of hepatocytes due to LPS caused the increase of AST and ALT in mouse plasma. In Ceramics group, however, the concentration of AST and ALT were much lower than LPS group until 6 weeks. And the losses of cytoplasm were rarely seen in Ceramics group. RT-PCR results showed that the decrease of proinflammatory cyto-kines such as IL-1β and IL-6 was observed in Ceramics group. Moreover, TGF-β1 and VEGF expression was increased in Ceramics group. Conclusion Bioactive ceramics effectively protected endotoxin-induced liver injury by attenuation of inflammatory processes in mice.
机译:研究目的据报道,一种生物活性陶瓷可调节脂多糖(LPS)活化的巨噬细胞中炎性细胞因子的表达。在本研究中,我们使用小鼠肝损伤模型研究了生物活性陶瓷的抗炎作用。材料和方法将小鼠分为三组:正常组,LPS组(LPS和未进行陶瓷处理),陶瓷组(LPS和陶瓷处理)。结果LPS给药可引起小鼠血浆天冬氨酸转氨酶(AST)和丙氨酸转氨酶(ALT)升高。 LPS引起的肝细胞胞质损失导致小鼠血浆AST和ALT升高。然而,在陶瓷组中,直到6周,AST和ALT的浓度远低于LPS组。陶瓷组细胞质的丢失很少见。 RT-PCR结果显示,陶瓷组的促炎细胞因子如IL-1β和IL-6减少。此外,陶瓷组的TGF-β1和VEGF表达增加。结论生物活性陶瓷可通过减轻小鼠的炎症过程有效地保护内毒素引起的肝损伤。

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  • 来源
    《Journal of materials science 》 |2009年第1期| 295-299| 共5页
  • 作者单位

    Research Institute of Biomedical Engineering, School of Medicine, Catholic University of Daegu, Daegu, South Korea;

    Research Institute of Biomedical Engineering, School of Medicine, Catholic University of Daegu, Daegu, South Korea;

    Research Institute of Biomedical Engineering, School of Medicine, Catholic University of Daegu, Daegu, South Korea;

    Research Institute of Biomedical Engineering, School of Medicine, Catholic University of Daegu, Daegu, South Korea;

    Division of Genome Resources, National Genome Research Institute, KNIH, Seoul, South Korea;

    The Research Center for Biomedical Resource of Oriental Medicine, Daegu Haany University, 162-4, Sang-Dong, Suseong-Gu, Daegu 706-828, South Korea;

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