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糖尿病肾病中,水通道蛋白-2尿排泄减少与尿浓缩能力受损相关。

Decrease in urinary excretion of aquaporin-2 associated with impaired urinary concentrating ability in diabetic nephropathy.

作者信息

Nakamura Tomoatsu, Saito Takako, Kusaka Ikuyo, Higashiyama Minori, Nagasaka Shoichiro, Ishibashi Shun, Ishikawa San-e

机构信息

Department of Medicine, Division of Endocrinology and Metabolism, Jichi Medical School, Tochigi, Japan.

出版信息

Nephron. 2002 Oct;92(2):445-8. doi: 10.1159/000063285.

Abstract

Aquaporin-2 (AQP-2) is known to be expressed in the renal collecting duct cells and participates in urinary concentration in response to arginine vasopressin (AVP). The present study was undertaken to determine whether progression of renal dysfunction affects urinary excretion of AQP-2 in diabetic nephropathy. The study was composed of 8 control subjects and 14 patients with type 2 diabetes classified into two groups according to serum creatinine level (cut-off point; 1.5 mg/dl). After an 8-hour water deprivation, both urinary osmolality (U(osm)) and urinary excretion of AQP-2 significantly decreased in the diabetic patients with chronic renal failure as compared to the control subjects (p < 0.0001, p < 0.05, respectively). After a water load (10 ml/kg), no differences were found in plasma osmolality (P(osm)), AVP levels and U(osm), whereas urinary excretion of AQP-2 significantly decreased in the patients with chronic renal failure as compared to the control subjects (p < 0.05). These results indicate that the decreased urinary excretion of AQP-2 in diabetic nephropathy is due to the impaired cellular signaling of AVP in collecting duct cells, which may be partly involved in the urinary concentrating defect in renal failure.

摘要

已知水通道蛋白-2(AQP-2)在肾集合管细胞中表达,并参与精氨酸加压素(AVP)介导的尿液浓缩过程。本研究旨在确定肾功能不全的进展是否会影响糖尿病肾病患者AQP-2的尿排泄。该研究包括8名对照受试者和14名2型糖尿病患者,根据血清肌酐水平(临界点:1.5mg/dl)分为两组。在禁水8小时后,与对照受试者相比,慢性肾衰竭糖尿病患者的尿渗透压(U(osm))和AQP-2的尿排泄均显著降低(分别为p<0.0001,p<0.05)。在水负荷(10ml/kg)后,血浆渗透压(P(osm))、AVP水平和U(osm)均无差异,而与对照受试者相比,慢性肾衰竭患者的AQP-2尿排泄显著降低(p<0.05)。这些结果表明,糖尿病肾病患者AQP-2尿排泄减少是由于集合管细胞中AVP的细胞信号传导受损,这可能部分参与了肾衰竭时的尿液浓缩缺陷。

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