Hypertension and Vascular Research Div., Dept. of Internal Medicine, Henry Ford Hospital, 2799 West Grand Blvd., Detroit, MI 48202, USA.
Am J Physiol Renal Physiol. 2010 Nov;299(5):F1185-92. doi: 10.1152/ajprenal.00112.2010. Epub 2010 Aug 18.
We showed that luminal flow stimulates nitric oxide (NO) production in thick ascending limbs. Ion delivery, stretch, pressure, and shear stress all increase when flow is enhanced. We hypothesized that shear stress stimulates NO in thick ascending limbs, whereas stretch, pressure, and ion delivery do not. We measured NO in isolated, perfused rat thick ascending limbs using the NO-sensitive dye DAF FM-DA. NO production rose from 21 ± 7 to 58 ± 12 AU/min (P < 0.02; n = 7) when we increased luminal flow from 0 to 20 nl/min, but dropped to 16 ± 8 AU/min (P < 0.02; n = 7) 10 min after flow was stopped. Flow did not increase NO in tubules from mice lacking NO synthase 3 (NOS 3). Flow stimulated NO production by the same extent in tubules perfused with ion-free solution and physiological saline (20 ± 7 vs. 24 ± 6 AU/min; n = 7). Increasing stretch while reducing shear stress and pressure lowered NO generation from 42 ± 9 to 17 ± 6 AU/min (P < 0.03; n = 6). In the absence of shear stress, increasing pressure and stretch had no effect on NO production (2 ± 8 vs. 8 ± 8 AU/min; n = 6). Similar results were obtained in the presence of tempol (100 μmol/l), a O(2)(-) scavenger. Primary cultures of thick ascending limb cells subjected to shear stresses of 0.02 and 0.55 dyne/cm(2) produced NO at rates of 55 ± 10 and 315 ± 93 AU/s, respectively (P < 0.002; n = 7). Pretreatment with the NOS inhibitor l-NAME (5 mmol/l) blocked the shear stress-induced increase in NO production. We concluded that shear stress rather than pressure, stretch, or ion delivery mediates flow-induced stimulation of NO by NOS 3 in thick ascending limbs.
我们发现管腔液流可刺激厚升支中的一氧化氮(NO)产生。当流量增加时,离子输送、牵张、压力和切应力均会增加。我们假设切应力可刺激厚升支产生 NO,而牵张、压力和离子输送则不会。我们使用 NO 敏感染料 DAF FM-DA 测量了分离灌注的大鼠厚升支中的 NO。当我们将管腔液流从 0 增加到 20 nl/min 时,NO 生成从 21 ± 7 增加到 58 ± 12 AU/min(P < 0.02;n = 7),但在停止液流 10 分钟后降至 16 ± 8 AU/min(P < 0.02;n = 7)。缺乏一氧化氮合酶 3(NOS 3)的小鼠的管腔液流不会增加 NO。用无离子溶液和生理盐水灌注的管腔液流以相同的程度刺激 NO 生成(20 ± 7 与 24 ± 6 AU/min;n = 7)。增加牵张而减少切应力和压力会使 NO 生成从 42 ± 9 降低至 17 ± 6 AU/min(P < 0.03;n = 6)。在没有切应力的情况下,增加压力和牵张对 NO 生成没有影响(2 ± 8 与 8 ± 8 AU/min;n = 6)。在使用 O(2)(-)清除剂 tempol(100 μmol/l)时也得到了类似的结果。分别以 0.02 和 0.55 达因/平方厘米的切应力作用于厚升支细胞的原代培养物,NO 的生成速率分别为 55 ± 10 和 315 ± 93 AU/s(P < 0.002;n = 7)。用 NOS 抑制剂 l-NAME(5 mmol/l)预处理可阻断切应力诱导的 NO 生成增加。我们得出结论,切应力而非压力、牵张或离子输送介导了厚升支中 NOS 3 介导的流量诱导的 NO 刺激。