Haley D P, Bulger R E, Dobyan D C
Virchows Arch B Cell Pathol Incl Mol Pathol. 1982;41(1-2):181-92. doi: 10.1007/BF02890280.
Studies were undertaken to determine the long-term effects of the nephrotoxin, uranyl nitrate, on the function and structure of the rat kidney. Animals were injected with 10 mg/kg B.Wt. of uranyl nitrate and renal function studies were performed one, two, four and eight weeks after drug administration. Light microscopy and scanning and transmission electron microscopy were used to characterize the morphologic changes at each time interval. Glomerular filtration rate was significantly reduced (P less than 0.01) one week (0.18 +/- 0.06 ml/min/100 gm B.Wt.) and two weeks (0.54 +/- 0.09 ml/min/100 gm B.Wt.) after drug treatment compared to controls (1.01 +/- 0.4 ml/min/100 gm B.Wt.) and returned to normal values by four weeks. The fractional excretion of sodium was significantly increased (P less than 0.01) one week after uranyl nitrate treatment (2.45% +/- 0.82) compared to controls (0.29% +/- 0.11). No further differences in this parameter were noted after one week. At all time intervals studied the pars recta of the proximal tubule (S2 and S3 segments) was the most consistently damaged region of the nephron. Acute tubular necrosis and tubular regeneration of these segments were evident one and two weeks after drug administration. Many of the tubules were widely dilated and lined by low-lying squamous epithelial cells. By four weeks some of these pars recta segments could be classified as microcysts and this type of lesion persisted as long as eight weeks after treatment. Regeneration of most injured proximal tubules was complete by eight weeks. Atrophic proximal tubules, marked interstitial fibrosis and a mononuclear cell infiltration, consistent with a chronic type of injury, were noted at the later time intervals. These results suggest that uranyl nitrate induces a persistent injury to the kidneys of rats causing lesions as long as eight weeks after injection.
开展了多项研究以确定肾毒素硝酸铀酰对大鼠肾脏功能和结构的长期影响。给动物注射10毫克/千克体重的硝酸铀酰,并在给药后1周、2周、4周和8周进行肾功能研究。使用光学显微镜、扫描电子显微镜和透射电子显微镜来描述每个时间间隔的形态学变化。与对照组(1.01±0.4毫升/分钟/100克体重)相比,药物治疗后1周(0.18±0.06毫升/分钟/100克体重)和2周(0.54±0.09毫升/分钟/100克体重)时肾小球滤过率显著降低(P<0.01),4周时恢复至正常水平。硝酸铀酰治疗1周后(2.45%±0.82)钠的分数排泄显著增加(P<0.01),而对照组为(0.29%±0.11)。1周后该参数未发现进一步差异。在所研究的所有时间间隔内,近端小管的直部(S2和S3段)是肾单位中最常受损的区域。给药后1周和2周,这些段出现明显急性肾小管坏死和肾小管再生。许多小管广泛扩张,内衬低平的鳞状上皮细胞。到4周时,一些直部段可归类为微囊肿,这种病变在治疗后长达8周持续存在。大多数受损近端小管在8周时再生完成。在后期时间间隔观察到萎缩的近端小管、明显的间质纤维化和单核细胞浸润,符合慢性损伤类型。这些结果表明,硝酸铀酰对大鼠肾脏诱导了持续性损伤,注射后长达8周仍会导致病变。