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Tumor necrosis factor-alpha induces renal cyclooxygenase-2 expression in response to hypercalcemia

机译:肿瘤坏死因子-α诱导肾环氧化酶-2响应高钙血症的表达

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摘要

The effect of tumor necrosis factor-alpha (TNF) on cyclooxygenase-2 (COX-2) expression in the renal outer medulla (OM) was determined in a model of dihydrotachysterol (DHT)-induced hypercalcemia. Increases in serum calcium and water intake were observed during ingestion of a DHT-containing diet in both wild type (WT) and TNF deficient mice (TNF−/−). Polyuria and a decrease in body weight were observed in response to DHT treatment in WT and TNF−/− mice. A transient elevation in urinary TNF was observed in WT mice treated with DHT. Moreover, increased urinary levels of prostaglandin E2 (PGE2) and a corresponding increase in COX-2 expression in the OM were observed in WT mice fed DHT. Increased COX-2 expression was not observed in TNF−/− mice fed DHT, and the characteristics of PGE2 synthesis were distinct from those in WT mice. This study demonstrates that COX-2 expression in the OM, secondary to hypercalemia, is TNF-dependent.
机译:在二氢速甾醇(DHT)诱导的高钙血症模型中确定了肿瘤坏死因子-α(TNF)对肾外延髓(OM)中环氧合酶2(COX-2)表达的影响。在野生型(WT)和TNF缺陷型小鼠(TNF -/-)中,摄入含DHT的饮食时,血清钙和水的摄入量增加。在WT和TNF -/-小鼠中,DHT处理可引起多尿和体重下降。在用DHT治疗的WT小鼠中观察到尿TNF的短暂升高。此外,在饲喂DHT的WT小鼠中,观察到尿中前列腺素E2(PGE2)的水平升高以及OM中COX-2表达的相应升高。在喂食DHT的TNF -/-小鼠中未观察到COX-2表达增加,并且PGE2合成的特征与野生型小鼠不同。这项研究表明,高钙血症继发于OM的COX-2表达是TNF依赖性的。

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