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实验性肾炎大鼠的药理学研究(9)。改良型Masugi肾炎中尿酶活性的变化及其来源。

Pharmacological studies on experimental nephritic rats (9). Changes in activities of urinary enzymes in the modified type of Masugi's nephritis and their sources.

作者信息

Ito M, Nagamatsu T, Suzuki Y

出版信息

Jpn J Pharmacol. 1980 Aug;30(4):471-9. doi: 10.1254/jjp.30.471.

Abstract

Using a modified model of Masugi's nephritis of rats, various enzymatic activities in urine, serum and renal tissue (glomeruli or cortex) were determined at appropriate intervals after the administration of anti-kidney serum and compared with the urinary protein content and the kidney weight. In the urine, alkaline phosphatase (Al-Phosase), acid phosphatase (Ac-Phosase) and N-acetyl-beta-glucosaminidase (NA-beta-Gase) activities remarkably increased after the induction of nephritis, reached their peaks on the 10th day and reverted to almost the normal levels on the 30th day. The patterns of time course of these enzymatic activities were similar to patterns seen in the urinary protein content and the kidney weight. In the serum, the Al-Phosase activity decreased slightly, while NA-beta-Gase activity increased slightly. The Ac-Phosase activity in serum remained at normal levels during the experimental periods. In the glomeruli, the bound activities of these three enzymes decreased with nephritis, showing a negative correlation with results in the urine. On the other hand, fibrinolytic activities in the urine (plasmin-like enzyme) and renal cortex (plasminogen activator) also paralleled the urinary protein content and the kidney weight in the course of the disease. These results suggest that the Al-Phosase, Ac-Phosase and NA-beta-Gase excreted into urine in cases of nephritis may be mostly derived from damaged renal cells and one part of Al-Phosase may also come from the plasma. Moreover, the increase of plasmin-like enzyme in urine is considered to be due to the increase of plasminogen activator in the renal cortex. Thus, the determination of these enzymatic activities in the urine should be useful for evaluating effects of drugs for the treatment of nephritis.

摘要

采用改良的大鼠Masugi肾炎模型,在给予抗肾血清后的适当时间间隔,测定尿液、血清和肾组织(肾小球或皮质)中的各种酶活性,并与尿蛋白含量和肾脏重量进行比较。在尿液中,肾炎诱导后碱性磷酸酶(Al-Phosase)、酸性磷酸酶(Ac-Phosase)和N-乙酰-β-氨基葡萄糖苷酶(NA-β-Gase)活性显著增加,在第10天达到峰值,第30天恢复到几乎正常水平。这些酶活性的时间进程模式与尿蛋白含量和肾脏重量的模式相似。在血清中,Al-Phosase活性略有下降,而NA-β-Gase活性略有增加。实验期间血清中的Ac-Phosase活性保持在正常水平。在肾小球中,这三种酶的结合活性随肾炎而降低,与尿液中的结果呈负相关。另一方面,尿液(纤溶酶样酶)和肾皮质(纤溶酶原激活剂)中的纤溶活性在疾病过程中也与尿蛋白含量和肾脏重量平行。这些结果表明,肾炎患者尿液中排出的Al-Phosase、Ac-Phosase和NA-β-Gase可能主要来源于受损的肾细胞,一部分Al-Phosase也可能来自血浆。此外,尿液中纤溶酶样酶的增加被认为是由于肾皮质中纤溶酶原激活剂的增加。因此,测定尿液中的这些酶活性对于评估治疗肾炎药物的效果应该是有用的。

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