Ibsen K K, Jensen H A, Wieth J O, Funder J
Hypertension. 1982 Sep-Oct;4(5):703-9. doi: 10.1161/01.hyp.4.5.703.
This report deals with the possibility that there is a specific change of the lithium transport across the membrane of erythrocytes from patients with essential hypertension. Sodium-lithium countertransport was significantly increased (p less than 0.005) in erythrocytes from 17 males with essential hypertension (mean 0.7 mmole (liter cells X hr)-1, range 0.4-1.6) compared to a group of 16 normotensive males (mean, 0.4 mmole (liter cells X hr)-1, range 0.3-0.6). A considerable overlap between the values from patients and controls was found. No significant increase of the transport function was found in a group of 14 female patients (mean 0.4 mmole (liter cells X hr)-1, range 0.2-0.6) compared with 10 normotensive female controls (mean 0.3 mmole (liter c hr)-1, range 0.3-0.6). A considerable overlap between the values from patients and controls was found. No significant increase of the transport function was found in a group of 14 female patients (mean 0.4 mmole (liter cells X hr)-1, range 0.2-0.6) compared with 10 normotensive female controls (mean 0.3 mmole (liter c hr)-1, range 0.3-0.6). A considerable overlap between the values from patients and controls was found. No significant increase of the transport function was found in a group of 14 female patients (mean 0.4 mmole (liter cells X hr)-1, range 0.2-0.6) compared with 10 normotensive female controls (mean 0.3 mmole (liter cells X hr)-1, range 0.1-0.6). Determination of sodium-lithium countertransport in red blood cells from nine children with and 14 without known familial disposition for essential hypertension did not demonstrate a close coupling between genetic disposition and the membrane transport function. In spite of the very small intraindividual variability of the transport function, studies of changes in sodium-lithium counter-transport are hampered by considerable interindividual variability of the transport in red cells from apparently normal individuals.
本报告探讨了原发性高血压患者红细胞膜上锂转运存在特定变化的可能性。与16名血压正常男性组成的对照组(平均值为0.4毫摩尔/(升细胞×小时),范围为0.3 - 0.6)相比,17名原发性高血压男性患者的红细胞钠 - 锂逆向转运显著增加(p < 0.005)(平均值为0.7毫摩尔/(升细胞×小时),范围为0.4 - 1.6)。患者与对照组的值存在相当大的重叠。与10名血压正常女性对照组(平均值为0.3毫摩尔/(升细胞×小时),范围为0.3 - 0.6)相比,14名女性患者组成的一组(平均值为0.4毫摩尔/(升细胞×小时),范围为0.2 - 0.6)未发现转运功能有显著增加。患者与对照组的值存在相当大的重叠。与10名血压正常女性对照组(平均值为0.3毫摩尔/(升细胞×小时),范围为0.1 - 0.6)相比,14名女性患者组成的一组(平均值为0.4毫摩尔/(升细胞×小时),范围为0.2 - 0.6)未发现转运功能有显著增加。患者与对照组的值存在相当大的重叠。对9名有原发性高血压家族倾向和14名无原发性高血压家族倾向的儿童的红细胞进行钠 - 锂逆向转运测定,未发现遗传倾向与膜转运功能之间有紧密联系。尽管转运功能的个体内变异性非常小,但由于明显正常个体红细胞转运的个体间变异性较大,钠 - 锂逆向转运变化的研究受到了阻碍。