Department of Internal Medicine and Education & Research Center, Kitasato University Medical Center, Kitamoto, Saitama, Japan.
Systems Biology Center, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, Maryland, United States of America.
PLoS One. 2013 Dec 23;8(12):e83146. doi: 10.1371/journal.pone.0083146. eCollection 2013.
Atrial natriuretic peptide (ANP) is known to influence NaCl transport in the medullary thick ascending limbs (MAL), where the largest NaCl reabsorption occurs among distal nephron segments in response to arginine vasopressin (AVP). In the present study, we investigated the effect of ANP on bicarbonate (HCO3 (-)) transport in the MAL using an isolated tubule perfusion technique. The HCO3 (-) concentration was measured using free-flow ultramicro-fluorometer. We first observed basal HCO3 (-) reabsorption in both long- and short-looped MALs (lMALs, and sMALs, respectively). AVP inhibited HCO3 (-) reabsorption in both lMALs and sMALs, whereas ANP did not change HCO3 (-) transport. However, in the presence of AVP, ANP restored the HCO3 (-) reabsorption inhibited by AVP both in lMAL and sMAL. The effects of ANP on HCO3 (-) transport was mimicked by cyclic GMP. The mRNA expression level of the vasopressin V2 receptor in lMALs was significantly higher than in sMALs, whereas expression of the V1a receptor was unchanged. In summary, AVP inhibits HCO3 (-) transport, and ANP counteracts the action of AVP on HCO3 (-) transport both in lMALs and sMALs.
心房利钠肽(ANP)已知会影响髓质升支粗段(MAL)中的 NaCl 转运,在远端肾单位中,MAL 是 NaCl 重吸收最大的部位,其对血管加压素(AVP)的反应。在本研究中,我们使用分离的管状灌注技术研究了 ANP 对 MAL 中碳酸氢盐(HCO3 (-))转运的影响。使用自由流动超微荧光计测量 HCO3 (-)浓度。我们首先观察了长和短环路 MAL(lMAL 和 sMAL)中的基础 HCO3 (-)重吸收。AVP 抑制了 lMAL 和 sMAL 中的 HCO3 (-)重吸收,而 ANP 并未改变 HCO3 (-)转运。然而,在 AVP 存在的情况下,ANP 恢复了 AVP 抑制的 lMAL 和 sMAL 中的 HCO3 (-)重吸收。cGMP 模拟了 ANP 对 HCO3 (-)转运的作用。lMAL 中的血管加压素 V2 受体的 mRNA 表达水平明显高于 sMAL,而 V1a 受体的表达则不变。总之,AVP 抑制 HCO3 (-)转运,而 ANP 拮抗 AVP 对 lMAL 和 sMAL 中 HCO3 (-)转运的作用。