Long-term effect of Heme oxygenase (HO)-1 induction in glomerular immune injury

Prasun K. Datta , Pu Duann , Elias A. Lianos
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引用次数: 14

Abstract

In a rat model of macrophage-dependent glomerular immune injury induced by administration of antibody against the glomerular basement membrane (anti-GBM), the authors assessed the anti-proteinuric effect of Heme Oxygenase-1 (HO-1) induction. Rats received anti-GBM antibody alone, anti-GBM antibody and treatment with the HO-1 inducer, hemin, or non-immune serum (controls). Urine protein, creatinine, and nitrite/nitrate excretion were measured on days 5, 7, and 14 after administration of the anti-GBM antibody. In hemin-treated animals with anti-GBM antibody-induced immune injury, HO-1 immunolocalized in macrophages infiltrating glomeruli and in tubular epithelial cells. In these animals, proteinuria was decreased. There was also a decrease in blood urea nitrogen (BUN) levels without a change in serum creatinine or systemic blood pressure. The observations establish the anti-proteinuric effect of hemin induction. This effect could be mechanistically linked to blunting of the ability of infiltrating macrophages to cause injury or to changes in tubular handling of filtered protein.

血红素加氧酶(HO)-1诱导对肾小球免疫损伤的远期影响
在给药抗肾小球基底膜抗体(anti-GBM)诱导的巨噬细胞依赖性肾小球免疫损伤大鼠模型中,作者评估了血红素加氧酶-1 (HO-1)诱导的抗蛋白尿作用。大鼠分别接受抗gbm抗体、抗gbm抗体和HO-1诱导剂、血红素或非免疫血清治疗(对照组)。在给予抗gbm抗体后第5、7、14天测定尿蛋白、肌酐和亚硝酸盐/硝酸盐排泄量。在抗gbm抗体诱导免疫损伤的hemin处理动物中,HO-1免疫定位于浸润肾小球的巨噬细胞和小管上皮细胞。在这些动物中,蛋白尿减少了。血尿素氮(BUN)水平也有所下降,但血清肌酐或全身血压没有变化。观察结果证实了血红素诱导的抗蛋白尿作用。这种效应可能与浸润性巨噬细胞造成损伤的能力减弱或滤过蛋白的小管处理改变有关。
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