Nielsen J R, Pedersen K E, Klitgaard N A, Johansen T
Department of Clinical Physiology, Odense University Hospital, Denmark.
Eur J Clin Invest. 1989 Feb;19(1):72-7. doi: 10.1111/j.1365-2362.1989.tb00198.x.
Lymphocytes were used as a cellular model for the in vitro measurements of maximal ouabain binding sites in order to assess any changes in young men at increased risk of developing essential hypertension, and to analyse whether any such changes were associated to borderline hypertension and/or heredity. Four groups were evaluated; 28 normotensive (NTO) and 20 borderline hypertensive (BHO) offspring of hypertensives. Twelve borderline hypertensives (BH) and 28 normotensive subjects (NT) with normotensive parents. The number of ouabain binding sites were significantly increased in the borderline hypertensives irrespective of heredity. The borderline hypertensives were heavier than the normotensives. A stepwise multiple regression model was therefore used in order to control confoundings by body mass index (BMI) and other factors such as age, gamma glutamyl transferase, 24 h sodium excretion, serum triglyceride, and serum cholesterol, which may influence the number of ouabain binding sites. Only BMI entered the stepwise model. These results indicate the presence of an increased number of sodium-potassium pumps in lymphocytes from borderline hypertensives. This difference may be attributed to the blood pressure disease or increased body mass.
淋巴细胞被用作体外测量哇巴因最大结合位点的细胞模型,以评估有患原发性高血压风险增加的年轻男性的任何变化,并分析任何此类变化是否与临界高血压和/或遗传有关。评估了四组;28名高血压患者的正常血压(NTO)后代和20名临界高血压(BHO)后代。12名临界高血压患者(BH)和28名父母血压正常的正常血压受试者(NT)。无论遗传情况如何,临界高血压患者的哇巴因结合位点数量均显著增加。临界高血压患者比正常血压患者更重。因此,使用逐步多元回归模型来控制体重指数(BMI)和其他因素(如年龄、γ-谷氨酰转移酶、24小时钠排泄、血清甘油三酯和血清胆固醇)的混杂影响,这些因素可能会影响哇巴因结合位点的数量。只有BMI进入了逐步模型。这些结果表明临界高血压患者淋巴细胞中钠钾泵的数量增加。这种差异可能归因于血压疾病或体重增加。