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人肝胞质中醛氧化酶活性和蛋白表达的发育变化。

Developmental changes of aldehyde oxidase activity and protein expression in human liver cytosol.

机构信息

Faculty of Pharmaceutical Science, Hiroshima International University, Kure, Japan.

出版信息

Drug Metab Pharmacokinet. 2012;27(5):543-7. doi: 10.2133/dmpk.dmpk-11-nt-124. Epub 2012 Mar 27.

Abstract

Aldehyde oxidase (AO) plays a role in metabolizing many drugs, such as methotrexate and 6-mercaptopurine. We previously showed that AO activity in rat liver rapidly increases from birth, reaching a plateau within 4 weeks, and is regulated at the protein expression level. However, developmental changes of AO activity and protein expression in human liver have not been reported. Here, we investigated the developmental changes and variability of AO in 16 human livers (13 children ranging from 13 days to 12 years old and 3 adults, 17, 34 and 45 years old). Young children (13 days to 4 months after birth) showed little liver AO activity, evaluated in terms of the activities for oxidation of N-1-methylnicotinamide to N-1-methyl-2-pyridone-5-carboxamide and N-1-methyl-4-pyridone-3-carboxamide in liver cytosol. However, these oxidase activities were markedly increased after 4 months, reaching the adult level by about 2 years of age. The AO band density in immunoblotting analysis was well correlated with the AO activity among all subjects (p < 0.01, r(2) = 0.771). Therefore, AO activity in the liver of young children is regulated at the AO protein expression level. Thus, as in rats, the AO activity in humans rapidly increases soon after birth, and is regulated at the protein expression level.

摘要

醛氧化酶 (AO) 在代谢许多药物方面发挥作用,如甲氨蝶呤和 6-巯基嘌呤。我们之前表明,大鼠肝脏中的 AO 活性从出生后迅速增加,在 4 周内达到稳定状态,并在蛋白质表达水平上受到调节。然而,尚未报道人肝脏中 AO 活性和蛋白表达的发育变化。在这里,我们研究了 16 个人肝脏中的 AO 的发育变化和可变性(13 名儿童从出生后 13 天到 12 岁,3 名成年人分别为 17、34 和 45 岁)。年幼的儿童(出生后 13 天至 4 个月)肝脏 AO 活性较低,通过评估肝胞质中 N-1-甲基烟酰胺氧化为 N-1-甲基-2-吡啶酮-5-羧酰胺和 N-1-甲基-4-吡啶酮-3-羧酰胺的活性来评估。然而,这些氧化酶活性在 4 个月后显著增加,到 2 岁左右达到成人水平。在所有受试者中,免疫印迹分析中的 AO 带密度与 AO 活性密切相关(p<0.01,r(2)=0.771)。因此,儿童肝脏中的 AO 活性在 AO 蛋白表达水平上受到调节。因此,与大鼠一样,人类的 AO 活性在出生后迅速增加,并在蛋白质表达水平上受到调节。

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