Conger J D, Falk S A, Guggenheim S J, Burke T J
J Clin Invest. 1976 Sep;58(3):681-9. doi: 10.1172/JCI108514.
The early pathophysiological changes in acute urate nephropathy were investigated in a rat model using micropuncture, clearance, and morphologic methods. Plasma urate was increased from 1.2 +/- 0.6 to 20.1 +/- 3.1 mg/100 ml (P less than 0.001). Urinary urate rose from 24.3 +/- 5.1 to 142.2 +/- 21.0 mg/100 ml (P less than 0.001). Renal plasma flow and glomerular filtration rate fell to 17 and 14% of control values, respectively, and urine flow rate decreased from 11.3 +/- 4.8 to 4.2 +/- 2.2 mul/min (all P less than 0.005) Superficial nephron filtration rate fell less than that of the whole kidney (70 vs. 86%). Both proximal and distal tubular pressures were increased from 10.6 to 26.1 mm Hg and from 7.2 to 24.7 mm Hg, respectively (P less than 0.005). Efferent arteriolar and peritubular capillary pressures were increased twofold. Vascular resistance beyond the peritubular capillaries increased from 4.8 X 10(9) to 21.6 X 10(9) dynes s/cm5. Extensive deposits of uric acid and urate were found in the tubular system and vasa recti from the corticomedullary junction to the tip of the papilla. It is concluded from these experiments that not only tubular obstruction in the collecting ducts, but also obstruction of the distal renal vasculature, are the primary early pathogenetic events in acute urate nephropathy.
利用微穿刺、清除率及形态学方法,在大鼠模型中研究了急性尿酸盐肾病早期的病理生理变化。血浆尿酸盐从1.2±0.6mg/100ml升高至20.1±3.1mg/100ml(P<0.001)。尿尿酸从24.3±5.1mg/100ml升至142.2±21.0mg/100ml(P<0.001)。肾血浆流量和肾小球滤过率分别降至对照值的17%和14%,尿流率从11.3±4.8μl/min降至4.2±2.2μl/min(所有P<0.005)。浅表肾单位滤过率下降幅度小于全肾(分别为70%和86%)。近端和远端肾小管压力分别从10.6mmHg升至26.1mmHg和从7.2mmHg升至24.7mmHg(P<0.005)。出球小动脉和肾小管周围毛细血管压力增加了两倍。肾小管周围毛细血管后的血管阻力从4.8×10⁹达因·秒/厘米⁵增至21.6×10⁹达因·秒/厘米⁵。在从皮质髓质交界处到乳头尖端的肾小管系统和直小血管中发现大量尿酸和尿酸盐沉积。从这些实验得出结论,急性尿酸盐肾病早期的主要发病机制不仅是集合管中的肾小管阻塞,还有远端肾血管阻塞。