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首页> 外文期刊>American Journal of Physiology >Chronic exposure to hypoxia attenuates renal injury and innate immunity activation in the remnant kidney model
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Chronic exposure to hypoxia attenuates renal injury and innate immunity activation in the remnant kidney model

机译:慢性接触缺氧衰减残余肾模型中的肾损伤和先天免疫激活

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Hypoxia is thought to influence the pathogenesis of chronic kidney disease, but direct evidence that prolonged exposure to tissue hypoxia initiates or aggravates chronic kidney disease is lacking. We tested this hypothesis by chronically exposing normal rats and rats with 5/6 nephrectomy (Nx) to hypoxia. In addition, we investigated whether such effect of hypoxia would involve activation of innate immunity. Adult male Munich-Wistar rats underwent Nx (n = 54) or sham surgery (sham; n = 52). Twenty-six sham rats and 26 Nx rats remained in normoxia, whereas 26 sham rats and 28 Nx rats were kept in a normobaric hypoxia chamber (12% O_2) for 8 wk. Hypoxia was confirmed by immunohistochemistry for pimonidazole. Hypoxia was confined to the medullary area in sham + normoxia rats and spread to the cortical area in sham + hypoxia rats, without changing the peritubular capillary density.
机译:缺氧被认为影响慢性肾病的发病机制,但直接证据表明延长了组织缺氧的发育,或加剧慢性肾病缺乏。 我们通过长期暴露于5/6肾切除术(NX)至缺氧的正常大鼠和大鼠来测试这一假设。 此外,我们调查了缺氧是否涉及激活先天免疫力。 成年雄性慕尼黑 - Wistar大鼠接受NX(n = 54)或假手术(假; n = 52)。 常氧留下26只假的大鼠和26只NX大鼠,而26只小鼠和28只NX大鼠在常见的缺氧室(12%O_2)中保持8周。 通过免疫组织化学对吡喃唑来证实缺氧。 缺氧被限制在假+常氧大鼠中的髓质区域,并扩散到假+缺氧大鼠的皮质区域,而不改变垂直毛细血管密度。

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