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慢性肾衰竭中的卟啉

Porphyrins in chronic renal failure.

作者信息

Day R S, Eales L

出版信息

Nephron. 1980;26(2):90-5. doi: 10.1159/000181958.

Abstract

A highly sensitive thin layer chromatographic assay was used to establish distinct anomalies in hepatic and renal prophyrin synthesis associated with chronic renal failure. Urinary and plasma coproporphyrin disappeared but plasma uroporphyrin (isomer III) levels rose. Patients on maintenance hemodialysis showed elevated red cell protoporphyrin and decreased total stool porphyrins whilst the raised plasma uroporphyrin did not pass into the dialysate, even in 2 cases of overt symptomatic porphyria. These results indicate that urinary coproporphyrin is of renal and not hepatic origin and that azotemia may reduce the activity of the enzyme uroporphyrinogen decarboxylase.

摘要

采用高灵敏度薄层色谱分析法,以确定与慢性肾衰竭相关的肝和肾卟啉合成的明显异常。尿和血浆中的粪卟啉消失,但血浆尿卟啉(异构体III)水平升高。维持性血液透析患者的红细胞原卟啉升高,粪便总卟啉降低,而升高的血浆尿卟啉即使在2例明显有症状的卟啉病患者中也未进入透析液。这些结果表明,尿粪卟啉来源于肾脏而非肝脏,氮质血症可能会降低尿卟啉原脱羧酶的活性。

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