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抗小鼠白细胞介素-6单克隆抗体和糖皮质激素受体拮抗剂RU38486对脂多糖处理小鼠血清金属硫蛋白诱导活性的阻断作用。

Blocking effect of anti-mouse interleukin-6 monoclonal antibody and glucocorticoid receptor antagonist, RU38486, on metallothionein-inducing activity of serum from lipopolysaccharide-treated mice.

作者信息

Itoh N, Kasutani K, Muto N, Otaki N, Kimura M, Tanaka K

机构信息

Faculty of Pharmaceutical Sciences, Osaka University, Japan.

出版信息

Toxicology. 1996 Aug 1;112(1):29-36. doi: 10.1016/0300-483x(96)03345-8.

Abstract

Although there is much evidence to suggest that lipopolysaccharide (LPS)-induced elevation of hepatic metallothionein (MT) contents is mediated by cytokines, the presence of MT-inducing activity in the serum of LPS-treated animals has not been examined. It was found that serum from LPS-treated mice stimulated MT induction in a hepatoma cell culture. The MT-inducing activity in serum was highest 2 h after LPS injection. Tumor necrosis factor and interleukin (IL)-6 levels in the serum were highest 1 and 2 h, respectively, after LPS injection. Anti-mouse IL-6 monoclonal antibody neutralized MT-inducing activity in serum obtained from mice 2 h after LPS injection. The MT-inducing activity in serum was blocked by the glucocorticoid antagonist, RU38486. A similar requirement for glucocorticoid was also observed in an IL-6-stimulated culture. These results show that the LPS-induced elevation of hepatic MT is mediated by IL-6, and the expression of the stimulating activity of IL-6 is dependent on the presence of glucocorticoid.

摘要

尽管有大量证据表明脂多糖(LPS)诱导的肝脏金属硫蛋白(MT)含量升高是由细胞因子介导的,但尚未检测LPS处理动物血清中MT诱导活性的存在情况。研究发现,LPS处理小鼠的血清可刺激肝癌细胞培养中的MT诱导。血清中的MT诱导活性在LPS注射后2小时最高。血清中的肿瘤坏死因子和白细胞介素(IL)-6水平分别在LPS注射后1小时和2小时最高。抗小鼠IL-6单克隆抗体可中和LPS注射后2小时从小鼠获得的血清中的MT诱导活性。血清中的MT诱导活性被糖皮质激素拮抗剂RU38486阻断。在IL-6刺激的培养中也观察到对糖皮质激素的类似需求。这些结果表明,LPS诱导的肝脏MT升高是由IL-6介导的,且IL-6刺激活性的表达依赖于糖皮质激素的存在。

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