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Oxygen-18 isotope of breath CO2 linking to erythrocytes carbonic anhydrase activity: a biomarker for pre-diabetes and type 2 diabetes

机译:呼吸道CO2的氧18同位素与红细胞碳酸酐酶活性相关:糖尿病前期和2型糖尿病的生物标志物

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摘要

Carbonic anhydrase (CA), a well-characterized metalloenzyme, is associated with oxygen-18 ( 18O)-isotopic fractionations of CO2. To investigate how CA activity links the 18O of breath CO2 to pre-diabetes (PD) and type 2 diabetes (T2D) during metabolism, we studied pre- and post-dose CA activities in erythrocytes with simultaneous monitoring of 18O/ 16O-isotope ratios of breath CO2 and thereafter elucidated potential metabolic pathways underlying CA alteration in the pathogenesis of T2D. Here we show that the post-dose CA activity in both T2D and PD was markedly enhanced, whereas the non-diabetic controls (NDC) exhibited a considerable reduction in post-dose CA activity when compared with their basal CA activities. However, T2D and PD exhibited isotopic enrichments of 18O in breath CO2, while a marked depletion of 18O in CO2 was manifested in NDC. Thus, the isotopic enrichments and depletions of 18O in breath CO2 were well correlated with the changes in CA activities for controls, PD and T2D. Our findings suggest the changes in CA activities in erythrocytes may contribute to the pathogenesis of T2D and the breath C 18O 16O regulated by the CA activity as a potential biomarker for non-invasive assessment of T2D, and thus may open a new method for treating T2D.
机译:碳酸酐酶(CA)是一种特征明确的金属酶,与CO-18的氧18( 18 O)同位素分馏有关。为研究CA活性如何在代谢过程中将呼吸CO2的 18 O与糖尿病前期(PD)和2型糖尿病(T2D)联系起来,我们研究了剂量前和给药后红细胞同时发生CA活动监测呼吸CO2的 18 O / 16 O同位素比率,并阐明在T2D发病机理中CA改变的潜在代谢途径。在这里,我们显示T2D和PD中的给药后CA活性均显着增强,而非糖尿病对照(NDC)与基础CA活性相比,给药后CA活性显着降低。然而,T2D和PD在呼吸中的CO2中表现出 18 O的同位素富集,而在NDC中则显示出CO2中 18 O的显着消耗。因此,呼吸二氧化碳中 18 O的同位素富集和耗竭与对照,PD和T2D的CA活性变化密切相关。我们的发现表明,红细胞中CA活性的变化可能是T2D的发病机理,CA活性调节的呼吸C 18 O 16 O可能是非糖尿病的潜在生物标志物。 -对T2D的侵入性评估,因此可能会开辟治疗T2D的新方法。

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