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半乳糖血症:继发于1-磷酸半乳糖尿苷转移酶缺乏的硫酸盐代谢改变。

Galactosemia: alterations in sulfate metabolism secondary to galactose-1-phosphate uridyltransferase deficiency.

作者信息

Tedesco T A, Miller K L

出版信息

Science. 1979 Sep 28;205(4413):1395-7. doi: 10.1126/science.472754.

Abstract

Cultures of nonmutant as well as galactokinase-deficient fibroblasts incorporate 20 percent more [35S]sulfate when galactose is substituted for glucose in the medium; galactose-1-phosphate uridyltransferase-deficient cells incorporate 65.5 percent less. In addition to incorporating less [35S]sulfate, the uridyltransferase-deficient cells showed significant accumulation of intracellular galactose-1-phosphate within 4 hours after galactose exposure. Under the same conditions, no difference in [3H]uridine incorporation was observed. This metabolic alteration, occurring in response to galactose exposure, may be related to the pathophysiology of classical galactosemia.

摘要

当培养基中的葡萄糖被半乳糖替代时,非突变型以及半乳糖激酶缺陷型成纤维细胞的培养物摄取的[35S]硫酸盐多20%;而半乳糖-1-磷酸尿苷转移酶缺陷型细胞摄取的则少65.5%。除了摄取较少的[35S]硫酸盐外,尿苷转移酶缺陷型细胞在接触半乳糖后4小时内细胞内半乳糖-1-磷酸出现显著积累。在相同条件下,未观察到[3H]尿苷摄取有差异。这种因接触半乳糖而发生的代谢改变可能与典型半乳糖血症的病理生理学有关。

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