Hypertension and Vascular Research, Department of Internal Medicine, Henry Ford Hospital, Detroit, Michigan; Center for Molecular Medicine and Genetics, School of Medicine, Wayne State University, Detroit, Michigan;
Department of Physiology and Biophysics, Case Western Reserve University, Cleveland, Ohio; and Universidad de Buenos Aires, Facultad de Farmacia y Bioquímica, Ciudad Autónoma de Buenos Aires, Argentina.
Am J Physiol Renal Physiol. 2015 Jan 15;308(2):F149-56. doi: 10.1152/ajprenal.00279.2014. Epub 2014 Nov 5.
Thick ascending limbs reabsorb 30% of the filtered NaCl load. Nitric oxide (NO) produced by NO synthase 3 (NOS3) inhibits NaCl transport by this segment. In contrast, chronic angiotensin II (ANG II) infusion increases net thick ascending limb transport. NOS3 activity is regulated by changes in expression and phosphorylation at threonine 495 (T495) and serine 1177 (S1177), inhibitory and stimulatory sites, respectively. We hypothesized that NO production by thick ascending limbs is impaired by chronic ANG II infusion, due to reduced NOS3 expression, increased phosphorylation of T495, and decreased phosphorylation of S1177. Rats were infused with 200 ng·kg(-1)·min(-1) ANG II or vehicle for 1 and 5 days. ANG II infusion for 5 days decreased NOS3 expression by 40 ± 12% (P < 0.007; n = 6) and increased T495 phosphorylation by 147 ± 26% (P < 0.008; n = 6). One-day ANG II infusion had no significant effect. NO production in response to endothelin-1 was blunted in thick ascending limbs from ANG II-infused animals [ANG II -0.01 ± 0.06 arbitrary fluorescence units (AFU)/min vs. 0.17 ± 0.02 AFU/min in controls; P < 0.01]. This was not due to reduced endothelin-1 receptor expression. Phosphatidylinositol 3,4,5-triphosphate (PIP3)-induced NO production was also reduced in ANG II-infused rats (ANG II -0.07 ± 0.06 vs. 0.13 ± 0.04 AFU/min in controls; P < 0.03), and this correlated with an impaired ability of PIP3 to increase S1177 phosphorylation. We conclude that in ANG II-induced hypertension NO production by thick ascending limbs is impaired due to decreased NOS3 expression and altered phosphorylation.
厚升支重吸收 30%的滤过氯化钠负荷。一氧化氮合酶 3 (NOS3) 产生的一氧化氮 (NO) 抑制该节段的氯化钠转运。相反,慢性血管紧张素 II (ANG II) 输注增加净厚升支转运。NOS3 活性受表达和 Thr495 (T495) 和 Ser1177 (S1177) 磷酸化变化调节,分别为抑制和刺激位点。我们假设,由于 NOS3 表达减少、T495 磷酸化增加和 S1177 磷酸化减少,慢性 ANG II 输注会损害厚升支的 NO 产生。大鼠接受 200 ng·kg(-1)·min(-1) ANG II 或载体输注 1 和 5 天。ANG II 输注 5 天可使 NOS3 表达减少 40 ± 12%(P < 0.007;n = 6),T495 磷酸化增加 147 ± 26%(P < 0.008;n = 6)。1 天的 ANG II 输注无明显作用。内皮素-1 刺激的厚升支 NO 产生在 ANG II 输注动物中减弱[ANG II-0.01 ± 0.06 任意荧光单位(AFU)/min 与对照组的 0.17 ± 0.02 AFU/min 相比;P < 0.01]。这不是由于内皮素-1 受体表达减少。PIP3 诱导的 NO 产生在 ANG II 输注大鼠中也减少(ANG II-0.07 ± 0.06 与对照组的 0.13 ± 0.04 AFU/min 相比;P < 0.03),这与 PIP3 增加 S1177 磷酸化的能力受损有关。我们的结论是,在 ANG II 诱导的高血压中,厚升支的 NO 产生受损,这是由于 NOS3 表达减少和磷酸化改变所致。