高渗生理盐水输注诱导健康人淋巴细胞Na+/H+抗体活化和胞质碱化。

R Düsing, S Leibhammer, G Hoffmann, H Vetter, W Siffert
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引用次数: 3

摘要

Na+/H+反端口是一种膜转运蛋白,它挤出细胞内的质子以换取细胞外的钠。其生理和病理生理作用的一些细节仍不清楚。实验证据表明,反向转运蛋白参与细胞体积的调节。因此,在本研究中,我们研究了9名健康志愿者在急性高渗(2.5%)生理盐水输注(4 mmol NaCl/kg超过120分钟)后淋巴细胞Na+/H+抗转运的活性。用荧光染料双羧基乙基羧基荧光素用钠+丙酸(5-40 mM)酸化细胞后测定抗港活性。高渗盐水诱导血浆渗透压显著升高(308.4 +/- 2.3 vs. 293.5 +/- 2.7 mOsm/kg;P < 0.01),血清钠+(150.8 + / - 3.7和138.9 + / - 0.5更易/公斤;P < 0.01), Cl-浓度(118.0 +/- 3.9 vs. 101.1 +/- 1.0 mmol/kg;P < 0.01)。细胞外高渗生理盐水刺激淋巴细胞Na+/H+反港活性,使Vmax从2.44 +/- 0.16增加到3.27 +/- 0.34 10(-3)s-1 (P < 0.01), pK从6.81 +/- 0.03增加到6.87 +/- 0.03 (P < 0.05)。除反port激活外,胞质碱化,高渗盐水处理前胞质pH平均为6.90 +/- 0.02,高渗盐水处理后胞质pH平均为6.99 +/- 0.02 (P < 0.01)。我们的研究结果首次表明,由于高渗NaCl负荷引起的急性细胞外高渗与刺激的淋巴细胞Na+/H+反港活性和细胞质碱化有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hypertonic saline infusion induces activation of the lymphocyte Na+/H+ antiport and cytosolic alkalinization in healthy human subjects.

The Na+/H+ antiport is a membrane transport protein that extrudes intracellular protons in exchange for extracellular sodium. Some details of its physiological and pathophysiological role remain poorly defined. Experimental evidence suggests that the antiporter is involved in the regulation of cell volume. In the present study, we therefore investigated the activity of the lymphocyte Na+/H+ antiport in nine healthy volunteers following acute hypertonic (2.5%) saline infusion (4 mmol NaCl/kg over 120 min). Antiport activity was measured after acidifying the cells with Na+ propionate (5-40 mM) using the fluorescent dye bis-carboxyethyl carboxyfluorescein. Hypertonic saline induced significant increases in plasma osmolality (308.4 +/- 2.3 vs. 293.5 +/- 2.7 mOsm/kg; P < 0.01), serum Na+ (150.8 +/- 3.7 vs. 138.9 +/- 0.5 mmol/kg; P < 0.01), and Cl- concentrations (118.0 +/- 3.9 vs. 101.1 +/- 1.0 mmol/kg; P < 0.01). Extracellular hypertonicity was followed by a stimulated activity of the lymphocyte Na+/H+ antiport with an increase in the apparent Vmax values from 2.44 +/- 0.16 to 3.27 +/- 0.34 10(-3) s-1 (P < 0.01) and a slight rise in pK, from 6.81 +/- 0.03 to 6.87 +/- 0.03 (P < 0.05) after hypertonic saline. In addition to antiport activation, cytosolic alkalinization was observed with cytosolic pH values averaging 6.90 +/- 0.02 before and 6.99 +/- 0.02 (P < 0.01) after hypertonic saline. Our results show for the first time that acute extracellular hypertonicity in man due to hypertonic NaCl loading is associated with a stimulated lymphocyte Na+/H+ antiport activity and cytosolic alkalinization.

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