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

机译:糖尿病肾病中水通道蛋白2的尿排泄减少与尿液浓缩能力受损有关。

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摘要

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.
机译:已知水通道蛋白2(AQP-2)在肾收集管细胞中表达,并响应于精氨酸加压素(AVP)参与尿液浓度。本研究旨在确定糖尿病肾病中肾功能不全的进展是否会影响AQP-2的尿排泄。该研究由8名对照受试者和14名2型糖尿病患者组成,根据血清肌酐水平(临界点; 1.5 mg / dl)分为两组。禁水8小时后,与对照组相比,患有慢性肾功能衰竭的糖尿病患者的尿渗透压(U(osm))和尿排泄AQP-2均显着降低(分别为p <0.0001,p <0.05 )。在加水(10 ml / kg)后,血浆渗透压(P(osm)),AVP水平和U(osm)均无差异,而慢性肾功能衰竭患者的尿中AQP-2排泄显着降低,因为与对照组相比(p <0.05)。这些结果表明,糖尿病性肾病中AQP-2的尿排泄减少是由于收集导管细胞中AVP的细胞信号传导受损,这可能部分参与了肾衰竭的尿液浓缩缺陷。

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