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别嘌呤醇治疗的次黄嘌呤磷酸核糖转移酶缺陷小鼠的肾脏表型

The renal phenotype of allopurinol-treated HPRT-deficient mouse.

作者信息

Zennaro Cristina, Tonon Federica, Zarattini Paola, Clai Milan, Corbelli Alessandro, Carraro Michele, Marchetti Marialaura, Ronda Luca, Paredi Gianluca, Rastaldi Maria Pia, Percudani Riccardo

机构信息

Department of Medical, Surgery and Health Sciences, Università degli Studi di Trieste, Trieste, Italy.

Department of Life Sciences, Università degli Studi di Trieste, Trieste, Trieste, Italy.

出版信息

PLoS One. 2017 Mar 10;12(3):e0173512. doi: 10.1371/journal.pone.0173512. eCollection 2017.

Abstract

Excess of uric acid is mainly treated with xanthine oxidase (XO) inhibitors, also called uricostatics because they block the conversion of hypoxanthine and xanthine into urate. Normally, accumulation of upstream metabolites is prevented by the hypoxanthine-guanine phosphoribosyltransferase (HPRT) enzyme. The recycling pathway, however, is impaired in the presence of HPRT deficiency, as observed in Lesch-Nyhan disease. To gain insights into the consequences of purine accumulation with HPRT deficiency, we investigated the effects of the XO inhibitor allopurinol in Hprt-lacking (HPRT-/-) mice. Allopurinol was administered in the drinking water of E12-E14 pregnant mothers at dosages of 150 or 75 μg/ml, and mice sacrificed after weaning. The drug was well tolerated by wild-type animals and heterozygous HPRT+/- mice. Instead, a profound alteration of the renal function was observed in the HPRT-/- model. Increased hypoxanthine and xanthine concentrations were found in the blood. The kidneys showed a yellowish appearance, diffuse interstitial nephritis, with dilated tubules, inflammatory and fibrotic changes of the interstitium. There were numerous xanthine tubular crystals, as determined by HPLC analysis. Oil red O staining demonstrated lipid accumulation in the same location of xanthine deposits. mRNA analysis showed increased expression of adipogenesis-related molecules as well as profibrotic and proinflammatory pathways. Immunostaining showed numerous monocyte-macrophages and overexpression of alpha-smooth muscle actin in the tubulointerstitium. In vitro, addition of xanthine to tubular cells caused diffuse oil red O positivity and modification of the cell phenotype, with loss of epithelial features and appearance of mesenchymal characteristics, similarly to what was observed in vivo. Our results indicate that in the absence of HPRT, blockade of XO by allopurinol causes rapidly developing renal failure due to xanthine deposition within the mouse kidney. Xanthine seems to be directly involved in promoting lipid accumulation and subsequent phenotype changes of tubular cells, with activation of inflammation and fibrosis.

摘要

尿酸过多主要用黄嘌呤氧化酶(XO)抑制剂治疗,这类抑制剂也被称为尿酸生成抑制剂,因为它们能阻止次黄嘌呤和黄嘌呤转化为尿酸盐。正常情况下,次黄嘌呤-鸟嘌呤磷酸核糖转移酶(HPRT)可防止上游代谢产物的积累。然而,正如在莱施-奈恩病中所观察到的,在存在HPRT缺乏的情况下,这种循环途径会受损。为了深入了解HPRT缺乏导致嘌呤积累的后果,我们研究了XO抑制剂别嘌醇对缺乏Hprt(HPRT-/-)小鼠的影响。在E12 - E14怀孕母鼠的饮用水中以150或75μg/ml的剂量给予别嘌醇,断奶后处死小鼠。野生型动物和杂合子HPRT+/-小鼠对该药物耐受性良好。相反,在HPRT-/-模型中观察到肾功能发生了严重改变。血液中次黄嘌呤和黄嘌呤浓度升高。肾脏呈现淡黄色外观,弥漫性间质性肾炎,肾小管扩张,间质有炎症和纤维化改变。通过高效液相色谱分析确定,有大量黄嘌呤管状结晶。油红O染色显示脂质在黄嘌呤沉积的相同位置积累。mRNA分析显示脂肪生成相关分子以及促纤维化和促炎途径的表达增加。免疫染色显示肾小管间质中有大量单核细胞-巨噬细胞以及α-平滑肌肌动蛋白过度表达。在体外,向肾小管细胞中添加黄嘌呤会导致弥漫性油红O阳性以及细胞表型改变,上皮特征丧失,出现间充质特征,这与体内观察到的情况类似。我们的结果表明,在缺乏HPRT的情况下,别嘌醇对XO的阻断会导致小鼠肾脏内黄嘌呤沉积,从而迅速发展为肾衰竭。黄嘌呤似乎直接参与促进脂质积累以及随后肾小管细胞的表型变化,并激活炎症和纤维化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4683/5345830/0f9d8e92c41a/pone.0173512.g001.jpg

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