Garrick R, Ziyadeh F N, Jorkasky D, Goldfarb S
Am J Nephrol. 1985;5(5):379-84. doi: 10.1159/000166967.
The most proximate defect responsible for the pathogenesis of Bartter's syndrome remains uncertain. Although an abnormality in chloride reabsorption in the thick ascending limb of Henle has been postulated, renal clearance studies performed during oral water loading failed to disclose a reduction in fractional chloride reabsorption. We alternatively postulate that the underlying abnormality may reside in a generalized increase in cell sodium permeability. Elevated levels of cell sodium may secondarily stimulate Na-K-ATPase activity. In the cells of the distal nephron, stimulated Na-K-ATPase would lead to enhanced potassium secretion into the tubular fluid producing the characteristic potassium depletion. In addition, increased cell sodium influx may stimulate a sodium-calcium exchanger. If this process exists in vascular smooth muscle, it may result in reduction of cytosolic calcium activity. This effect and/or chronic potassium depletion may mediate the reduced vascular reactivity characteristic of this syndrome.
导致巴特综合征发病机制的最直接缺陷仍不明确。尽管有人推测髓袢升支粗段的氯离子重吸收存在异常,但在口服水负荷期间进行的肾脏清除率研究未能揭示氯离子重吸收率的降低。我们转而推测潜在的异常可能在于细胞钠通透性的普遍增加。细胞内钠水平升高可能继而刺激钠钾ATP酶活性。在远端肾单位的细胞中,受刺激的钠钾ATP酶会导致更多的钾分泌到肾小管液中,从而产生特征性的钾缺乏。此外,细胞钠内流增加可能会刺激钠钙交换体。如果这个过程存在于血管平滑肌中,可能会导致细胞质钙活性降低。这种效应和/或慢性钾缺乏可能介导了该综合征特征性的血管反应性降低。