Lee S M, Hillman B J, Clark R L, Michael U F
Invest Radiol. 1985 Dec;20(9):961-70. doi: 10.1097/00004424-198512000-00014.
To evaluate the effects of pharmacologic vasodilatation on glycerol-induced acute renal failure, we studied untreated animals and those given Captopril and Diltiazem at periods ranging from 30 minutes to four weeks after the onset of acute renal failure. At each time frame, comparative coded assessments of renal function, histology, and microangiography were performed. Diltiazem, a calcium channel blocker, significantly reduced the severity of the renal failure, decreased the extent of tubular cell necrosis, and was associated with a more rapid histologic and functional recovery. Captopril, an angiotensin converting enzyme inhibitor, did not influence renal function or pathology throughout the four-week observation period. Microangiography revealed marked differences among the experimental groups. Most notably, there was better visualization of the microvasculature in Diltiazem-treated kidneys at one and two weeks. However, at four weeks, all groups showed similar, severe microangiographic abnormalities. Diltiazem offers significant protection against glycerol-induced acute renal failure in rats. Its mechanism of action in this context remains unknown. Renal function and pathology do not correlate well with microangiographic perfusion patterns in this model of acute renal failure.
为评估药物性血管舒张对甘油诱导的急性肾衰竭的影响,我们研究了未治疗的动物以及在急性肾衰竭发作后30分钟至四周期间给予卡托普利和地尔硫䓬的动物。在每个时间点,对肾功能、组织学和微血管造影进行了对比编码评估。钙通道阻滞剂地尔硫䓬显著降低了肾衰竭的严重程度,减少了肾小管细胞坏死的范围,并与更快的组织学和功能恢复相关。血管紧张素转换酶抑制剂卡托普利在四周的观察期内未影响肾功能或病理变化。微血管造影显示各实验组之间存在显著差异。最值得注意的是,在一周和两周时,地尔硫䓬治疗的肾脏中微血管的显影更好。然而,在四周时,所有组均显示出相似的严重微血管造影异常。地尔硫䓬对大鼠甘油诱导的急性肾衰竭具有显著的保护作用。其在这种情况下的作用机制尚不清楚。在这种急性肾衰竭模型中,肾功能和病理与微血管造影灌注模式的相关性不佳。