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首页> 外文期刊>Comparative Medicine >Renal Function and Hematology in Rats with Congenital Renal Hypoplasia
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Renal Function and Hematology in Rats with Congenital Renal Hypoplasia

机译:先天性肾发育不全大鼠的肾功能和血液学

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摘要

Renal hypoplasia due to a congenitally reduced number of nephrons progresses to chronic kidney disease and may cause renal anemia, given that the kidneys are a major source of erythropoietin in adults. Hypoplastic kidney (HPK) rats have only about 20% of the normal number of nephrons and develop CKD. This study assessed the renal function and hematologic changes in HPK rats from 70 to 210 d of age. HPK rats demonstrated deterioration of renal excretory function, slightly macrocytic erythropenia at all days examined, age-related increases in splenic hemosiderosis accompanied by a tendency toward increased hemolysis, normal plasma erythropoietin levels associated with increased hepatic and decreased renal erythropoietin production, and maintenance of the response for erythropoietin production to hypoxic conditions, with increased interstitial fibrosis at 140 d of age. These results indicate that increases in splenic hemosiderosis and the membrane fragility of RBC might be associated with erythropenia and that hepatic production of erythropoietin might contribute to maintaining the blood Hgb concentration in HPK rats.
机译:由于肾脏是成年人中促红细胞生成素的主要来源,因此,由于肾单位数量的减少而导致的肾发育不全会发展为慢性肾脏疾病,并可能导致肾脏贫血。发育不良的肾脏(HPK)大鼠只有约20%的正常肾单位发展为CKD。这项研究评估了70至210 d年龄的HPK大鼠的肾功能和血液学变化。 HPK大鼠表现出肾脏排泄功能恶化,所有检查天均出现轻度巨噬细胞性红血球减少,与年龄相关的脾性铁血黄素沉着症增加,溶血倾向增加,血浆正常促红细胞生成素水平与肝脏增加和肾促红细胞生成素生成减少有关以及维持缺氧条件下促红细胞生成素生成的反应,在140 d时间质纤维化增加。这些结果表明,脾血铁血黄素沉着增加和红细胞膜脆性可能与红血球减少有关,并且肝脏产生的促红细胞生成素可能有助于维持HPK大鼠的血Hgb浓度。

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