Na-Li反转运活性异常高血压患者亲属的Na-Li反转运动力学

Peter A. Rutherford , Trevor H. Thomas, Robert Wilkinson
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引用次数: 3

摘要

家族因素被认为是决定高钠锂反转运活性(定义为>0.40 mmol Li/(h × l细胞),外部钠浓度为140 mmol/ l (Nae140))的重要因素,这在一定比例的原发性高血压患者中观察到。然而,环境因素如怀孕和血脂异常也会影响运动。原发性高血压患者高钠锂反转运活性(Nae140)主要是由于Michaelis常数(Km)低,并与高vmax / kratio相关。相反,血脂异常会影响vmax。本研究旨在确定是否有证据表明kmandvmax / kmrratio受家族因素的影响。对12例钠锂反转运动力学异常的高血压先证者的47例一级亲属和35例正常对照组进行了钠锂反转运动力学测定。钠锂反转运是通过钠刺激的锂离子从载锂红细胞外排来测量的。与正常受试者相比,亲属的kmax / km显著降低,vmax / km显著增加。11个亲属具有高钠锂反转运活性(Nae140),与低kmax /Km和高vmax /Km相关。14例高血压亲属均有钠锂反转运动力学异常。本研究的结果表明,家族因素在决定kmandvmax /Kmof钠锂反转运活性方面是重要的。旨在确定钠锂反转运的遗传及其作为原发性高血压中间表型的研究必须测量其动力学决定因素,以减少其他变量混淆效应的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Na–Li Countertransport Kinetics in the Relatives of Hypertensive Patients with Abnormal Na–Li Countertransport Activity

Familial factors are believed to be important in determining the high sodium–lithium countertransport activity (defined as >0.40 mmol Li/(h × l cell) at external sodium concentration of 140 mmol/L (Nae140)) which is observed in a proportion of patients with essential hypertension. However, environmental factors such as pregnancy and dyslipidemia also affect activity. High sodium–lithium countertransport activity (Nae140) in essential hypertension is mainly due to a low Michaelis constant (Km) and is associated with a highVmax/Kmratio. In contrast, dyslipidemias affectVmax. This study aimed to determine if there was evidence thatKmandVmax/Kmratios are influenced by familial factors. Sodium–lithium countertransport kinetics were measured in the 47 first degree relatives of 12 hypertensive probands with abnormal sodium–lithium countertransport kinetics and 35 normotensive control subjects. Sodium–lithium countertransport was measured as Na-stimulated Li efflux from lithium loaded erythrocytes. The relatives had significantly reducedKmand increasedVmax/Kmcompared to normal subjects. Eleven relatives had high sodium–lithium countertransport activity (Nae140), associated with lowKmand highVmax/Km. The 14 relatives that were hypertensive had abnormalities of sodium–lithium countertransport kinetics. The results of this study suggest that familial factors are important in determining theKmandVmax/Kmof sodium–lithium countertransport activity. Studies aimed at determining the inheritance of sodium–lithium countertransport and its use as an intermediate phenotype of essential hypertension must measure its kinetic determinants to reduce the risk of confounding effects from other variables.

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