首页> 外文期刊>World Journal of Gastroenterology >Production of reactive oxygen species and expression of inducible nitric oxide synthase in rat isolated Kupffer cells stimulated by Leptospira interrogans and Borrelia burgdorferi.
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Production of reactive oxygen species and expression of inducible nitric oxide synthase in rat isolated Kupffer cells stimulated by Leptospira interrogans and Borrelia burgdorferi.

机译:在问号钩端螺旋体和伯氏疏螺旋体刺激的大鼠分离的库普弗细胞中,活性氧的产生和诱导型一氧化氮合酶的表达。

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AIM: To evaluate the production of reactive oxygen species (ROS) and the expression of inducible nitric oxide synthase (iNOS) in rat isolated Kupffer cells (KCs) stimulated by Leptospira interrogans and Borrelia burgdorferi. METHODS: Rat Kupffer cells were separated by perfusion of the liver with 0.05% collagenase, and purified by Percoll gradients. Purified Kupffer cells were tested in vitro with alive L. interogans and B. burgdorferi preparations. The production of ROS was determined by chemiluminescence, whereas iNOS protein expression was evaluated by Western blot assay using anti-iNOS antibodies. RESULTS: B. burgdorferi and to a less extent L. interrogans induced ROS production with a peak 35 min after infection. The chemiluminescence signal progressively diminished and was undetectable by 180 min of incubation. Leptospirae and borreliae induced an increased iNOS expression in Kupffer cells that peaked at 6 hours and was still evident 22 h after infection. CONCLUSION: Both genera of spirochetes induced ROS and iNOS production in rat Kupffer cells. Since the cause of liver damage both in leptospiral as well as in borrelial infections are still unknown, we suggest that leptospira and borrelia damage of the liver can be initially mediated by oxygen radicals, and is then maintained at least in part by nitric oxide.
机译:目的:评估在问号钩端螺旋体和伯氏疏螺旋体刺激下的大鼠分离的库普弗细胞(KCs)中活性氧(ROS)的产生和诱导型一氧化氮合酶(iNOS)的表达。方法:用0.05%胶原酶灌注肝脏分离大鼠库普弗细胞,并通过Percoll梯度纯化。纯化的库普弗细胞在体外用活的L. interogans和B. burgdorferi制剂进行测试。 ROS的产生是通过化学发光来确定的,而iNOS蛋白的表达是通过使用抗iNOS抗体的蛋白质印迹分析来评估的。结果:B。burgdorferi和较少程度的问号L. interrogans诱导ROS产生,感染后35分钟达到峰值。化学发光信号逐渐减弱,孵育180分钟无法检测到。钩端螺旋体和疏螺旋体诱导枯否细胞中iNOS表达增加,在感染后6小时达到峰值,并在感染后22小时仍然明显。结论:螺旋属均诱导大鼠枯否细胞中ROS和iNOS的产生。由于在钩端螺旋体感染和疏螺旋体感染中造成肝损伤的原因仍然未知,我们建议肝的钩端螺旋体和疏螺旋体损伤最初可以由氧自由基介导,然后至少部分由一氧化氮维持。

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