Rutherford P A, Thomas T H, Wilkinson R
Department of Medicine (Nephrology), University of Newcastle upon Tyne, Newcastle upon Tyne, United Kingdom.
Biochem Mol Med. 1997 Oct;62(1):106-12. doi: 10.1006/bmme.1997.2617.
Familial factors are believed to be important in determining the high sodium-lithium countertransport activity (defined as >0.40 mmol Li/(h x l cell) at external sodium concentration of 140 mmol/L (Nae 140)) 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 (Nae 140) in essential hypertension is mainly due to a low Michaelis constant (Km) and is associated with a high Vmax/Km ratio. In contrast, dyslipidemias affect Vmax. This study aimed to determine if there was evidence that Km and Vmax/Km ratios 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 reduced Km and increased Vmax/Km compared to normal subjects. Eleven relatives had high sodium-lithium countertransport activity (Nae 140), associated with low Km and high Vmax/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 the Km and Vmax/Km of 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.
家族因素被认为在决定高钠 - 锂逆向转运活性(定义为在外部钠浓度为140 mmol/L(钠140)时>0.40 mmol锂/(小时×1个细胞))中起重要作用,这种高钠 - 锂逆向转运活性在一部分原发性高血压患者中可见。然而,诸如妊娠和血脂异常等环境因素也会影响该活性。原发性高血压中的高钠 - 锂逆向转运活性(钠140)主要归因于低米氏常数(Km),并与高Vmax/Km比值相关。相比之下,血脂异常影响Vmax。本研究旨在确定是否有证据表明Km和Vmax/Km比值受家族因素影响。在12名钠 - 锂逆向转运动力学异常的高血压先证者的47名一级亲属和35名血压正常的对照受试者中测量了钠 - 锂逆向转运动力学。钠 - 锂逆向转运通过测量钠刺激的锂从负载锂的红细胞中的流出量来测定。与正常受试者相比,这些亲属的Km显著降低,Vmax/Km升高。11名亲属具有高钠 - 锂逆向转运活性(钠140),与低Km和高Vmax/Km相关。14名高血压亲属存在钠 - 锂逆向转运动力学异常。本研究结果表明,家族因素在决定钠 - 锂逆向转运活性的Km和Vmax/Km方面很重要。旨在确定钠 - 锂逆向转运的遗传方式及其作为原发性高血压中间表型用途的研究必须测量其动力学决定因素,以降低来自其他变量的混杂效应风险。