Grossman E B, Hebert S C
Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts 02115.
J Clin Invest. 1988 Mar;81(3):885-92. doi: 10.1172/JCI113399.
This study investigates the effect of variations in mineralocorticoid as well as cell sodium delivery and uptake on Na-K-ATPase activity in the mouse medullary thick ascending limb of Henle (mTALH). Pharmacologic doses of the mineralocorticoid deoxycorticosterone acetate (DOCA) resulted in a 28% increase of Na-K-ATPase activity. Furosemide-induced inhibition of sodium uptake by the mTALH cell also resulted in Na-K-ATPase activity reduction (45%). Sodium deprivation did not cause a clear change in enzyme activity, either at 3 d or 2 wk, likely reflecting the result of the opposing influences of decreased sodium delivery and increased endogenous aldosterone. Finally, the behavior of Na-K-ATPase activity at 3 d of sodium deprivation in the mTALH contrasted with a 60% increase in activity observed in the cortical collecting tubule, a nephron segment known to be responsive to mineralocorticoid, and this heterogeneity of response may suggest an important role for the mTALH in maintaining salt homeostasis.
本研究调查了盐皮质激素的变化以及细胞钠转运和摄取对小鼠髓袢升支粗段(mTALH)中钠钾ATP酶活性的影响。药理剂量的盐皮质激素醋酸脱氧皮质酮(DOCA)使钠钾ATP酶活性增加了28%。呋塞米诱导的mTALH细胞钠摄取抑制也导致钠钾ATP酶活性降低(45%)。钠缺乏在3天或2周时均未引起酶活性的明显变化,这可能反映了钠转运减少和内源性醛固酮增加的相反影响的结果。最后,mTALH在钠缺乏3天时钠钾ATP酶活性的表现与皮质集合管中观察到的活性增加60%形成对比,皮质集合管是已知对盐皮质激素有反应的肾单位节段,这种反应的异质性可能表明mTALH在维持盐稳态中起重要作用。