Graduate Institute of Clinical Medicine, National Taiwan University College of Medicine, Taipei, Taiwan.
Department of Internal Medicine, National Taiwan University Hospital and College of Medicine, Taipei, Taiwan.
Sci Rep. 2016 Sep 7;6:32787. doi: 10.1038/srep32787.
Previous studies have shown that sirtuin 1 (Sirt1) is renoprotective; however, details regarding its distribution and functions in the kidney remain unknown. Here, we demonstrated that Sirt1 was mainly expressed in the tubulointerstitial cells of normal rat kidneys and was co-localized with aquaporin 2, indicating it may be involved in water/salt regulation. Renal Sirt1 expression increased in the non-glomerular cytoplasmic portion of the kidney after a 24-h fast, but no significant changes in Sirt1 expression occurred after water loading (50 mL/kg) or 24-h water deprivation. After consuming a low-salt (0.075%) or 60% calorie restriction diet for 7 days, Sirt1 expression in the rat kidney was significantly increased, whereas a high-salt (8%) diet did not change the level of Sirt1 expression. The low-salt diet also increased Sirt1 expression in the heart, muscle, brain, and fat tissues. The increased Sirt1 that was observed in rats on a low-salt diet was associated with increased ghrelin expression in the distal nephron, with both molecules exhibiting similar distribution patterns. An in vitro experiment suggested that ghrelin increases Sirt1 expression in cortical collecting duct cells by activating ghrelin receptors. Our study indicates that this 'ghrelin-Sirt1 system' may participate in regulating sodium reabsorption in the distal nephron.
先前的研究表明,Sirtuin 1(Sirt1)具有肾脏保护作用;然而,其在肾脏中的分布和功能仍不清楚。本研究表明,Sirt1 主要表达于正常大鼠肾脏的肾小管间质细胞,且与水通道蛋白 2 共定位,提示其可能参与水盐调节。禁食 24 h 后,肾脏非肾小球细胞质部分的 Sirt1 表达增加,但水负荷(50 ml/kg)或 24 h 限水后 Sirt1 表达无明显变化。7 天低盐(0.075%)或 60%热量限制饮食后,大鼠肾脏 Sirt1 表达显著增加,而高盐(8%)饮食并未改变 Sirt1 表达水平。低盐饮食还增加了心脏、肌肉、大脑和脂肪组织中的 Sirt1 表达。低盐饮食大鼠 Sirt1 表达增加与远端肾单位中 ghrelin 表达增加有关,两种分子表现出相似的分布模式。体外实验表明,ghrelin 通过激活 ghrelin 受体增加皮质集合管细胞中 Sirt1 的表达。本研究表明,该“ghrelin-Sirt1 系统”可能参与调节远端肾单位的钠重吸收。