%0 Journal Article
%T 急性马兜铃酸I中毒小鼠肾小管上皮细胞损伤变化<br>Changes in Renal Tubular Epithelial Cell Injury in Mice with Acute Aristolochic Acid I Intoxication
%A 兰爱琳
%A 王一凡
%A 李小芬
%A 黄春华
%A 楼迪栋
%J Advances in Clinical Medicine
%P 2236-2241
%@ 2161-8720
%D 2024
%I Hans Publishing
%R 10.12677/acm.2024.1441287
%X 为连续观察急性马兜铃酸I (Aristolochic Acids I, AAI)中毒时小鼠肾脏病理学改变，本实验将40只KM小鼠分为5组：对照组、AAI暴露2、4、6、8天组，AAI组小鼠以5 mg/kg/2d AAI灌胃模拟急性马兜铃酸肾病(Aristolochic Acid Nephropathy, AAN)，使各组小鼠AAI累积剂量分别为5、10、15、20 mg/kg。分别于AAI暴露2、4、6、8天处死，检测其肾功能指标肌酐(Creatinine, Cre)和尿素氮(Blood Urea Nitrogen, BUN)，并观察肾脏病理学改变。结果显示，与对照组相比，AAI各组小鼠Cre和BUN均呈剂量依赖性上升，Cre于第6、8天具有显著性差异(<i>P</i><i> </i>&lt; 0.05)；BUN于第4、6、8天具有显著性差异(<i>P</i><i> </i>&lt; 0.05)。AAI组小鼠主要病理变化为肾小管上皮细胞顶端微绒毛脱落、细胞水肿、坏死脱落。本研究发现暴露于AAI的小鼠肾小管损伤程度与AAI累积剂量呈正相关。<br />
In order to continuously observe the renal pathological changes in mice during acute aristolochic acids I (AAI) intoxication, 40 KM mice were divided into 5 groups: control group, AAI exposed for 2, 4, 6, and 8 days, and mice in the AAI group were simulated with acute aristolochic acid nephropathy (AAN) by gavage of 5 mg/kg/2d AAI, and the cumulative dose of AAI in each group was 5, 10, 15, and 20 mg/kg, respectively. Mice in the AAI group were put to death on 2, 4, 6, and 8 days of exposure to AAI to test their renal function indexes of creatinine (Cre) and blood urea nitrogen (BUN) and to observe the renal pathological changes. The results showed that compared with the control group, Cre and BUN increased in a dose-dependent manner in the AAI group, with significant differences in Cre on days 6 and 8 (<i>P</i> &lt; 0.05) and BUN on days 4, 6 and 8 (<i>P</i> &lt; 0.05). The main pathological changes in the AAI group were detachment of microvilli from the tips of renal tubular epithelial cells, cellular edema, and necrotic detachment. In this study, we found that the degree of renal tubular injury in mice exposed to AAI was positively correlated with the cumulative dose of AAI.
%K 马兜铃酸I，马兜铃酸肾病，肾小管上皮细胞，损伤<br>Aristolochic Acid I
%K Aristolochic Acid Nephropathy
%K Renal Tubular Epithelial Cells
%K Injury
%U http://www.hanspub.org/journal/PaperInformation.aspx?PaperID=85568