利用家猫短暂性单侧肾缺血和延迟性对侧肾切除术建立输尿管间质纤维化模型

Comparative medicine Pub Date : 2024-08-01 Epub Date: 2024-06-20 DOI:10.30802/AALAS-CM-24-000025
Bianca N Lourenço, Vanna M Dickerson, Cathy A Brown, Daniel R Rissi, Jennifer M Heathcote, Jonathan E Hare, Scott A Brown, Chad W Schmiedt
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摘要

肾小管间质纤维化是猫慢性肾病(CKD)的典型组织学特征,也是走向终末期肾病的最终常见途径。家猫已被用于缺血诱导的肾脏纤维化模型。本研究的目的是评估一过性单侧肾缺血和延迟性对侧肾切除这两种猫肾小管间质纤维化模型的表现。特意饲养的年轻成年驯化猫接受了手术诱导的右肾缺血 90 分钟,然后在缺血后 21 天(RI-CN21d 组;n = 10)或 90 天(RI-CN90d 组;n = 12)进行了延迟对侧肾切除术。对照组猫在缺血 21 天后接受假手术,然后进行左肾切除术(假-CN 组;n = 3)。手术前后评估了肾功能参数,包括肾小球滤过率和血清肌酐浓度。缺血/缺血后120天收获右肾。对收获的肾脏进行了肾组织学检查和病变评分,并通过组织形态计量学对平滑肌肌动蛋白免疫标记和胶原染色进行了量化。RI-CN21d 组、RI-CN90d 组和假 CN 组分别有 5/10 只(50.0%)、2/12 只(16.7%)和 0/3 只(0%)猫在左肾切除术后因严重急性肾损伤而安乐死。到 120 天时,RI-CN21d 组(P < 0.001)和 RI-CN90d 组(P < 0.001)的猫肾小球滤过率与基线相比明显下降,而假 CN 组(P = 0.76)则没有。研究结束时,除一只猫外,所有缺血组的猫都出现了氮质血症。与假手术肾脏相比,缺血肾脏的间质炎症、肾小管萎缩和纤维化评分更高。与对侧肾脏相比,这些肾脏的平滑肌肌动蛋白免疫标记和胶原染色明显增加。总之,90 分钟的单侧肾缺血和延迟的对侧肾切除术会诱发与猫慢性肾功能衰竭一致的组织学和生化变化。在缺血和肾切除术之间间隔 90 天可提高模型的存活率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of a Model of Tubulointerstitial Fibrosis Using Transient Unilateral Renal Ischemia and Delayed Contralateral Nephrectomy in Domesticated Cats.

Tubulointerstitial fibrosis is a classic histologic feature of chronic kidney disease (CKD) in cats and a final common pathway toward end-stage renal disease. Domesticated cats have been used in models of ischemia-induced renal fibrosis. The objective of this study was to evaluate the performance of 2 variations of a transient unilateral renal ischemia and delayed contralateral nephrectomy model of tubulointerstitial fibrosis in cats. Purpose-bred, young adult, domesticated cats underwent 90 min of surgically induced ischemia to the right kidney followed by delayed contralateral nephrectomy performed 21 d (RI-CN21d group; n = 10) or 90 d postischemia (RI-CN90d group; n = 12). Control cats underwent sham surgery followed by left nephrectomy 21 d after (sham-CN group; n = 3). Renal functional parameters, including glomerular filtration rate and serum creatinine concentration, were evaluated before and after surgeries. The right kidneys were harvested 120 d postischemia/ sham. Renal histology with lesion scoring and histomorphometry for quantification of smooth muscle actin immunolabeling and collagen staining were performed on harvested kidneys. Severe acute kidney injury prompted euthanasia after left nephrectomy in 5/10 (50.0%), 2/12 (16.7%), and 0/3 (0%) of cats in the RI-CN21d, RI-CN90d, and sham-CN groups, respectively. A significant decrease in glomerular filtration rate by day 120, relative to baseline, occurred in cats in the RI-CN21d group (P < 0.001) and RI-CN90d group (P < 0.001) but not the sham-CN group (P = 0.76). All but one cat in the ischemia groups were azotemic at the study end. Kidneys subjected to ischemia had higher interstitial inflammation, tubular atrophy, and fibrosis scores compared with sham-operated kidneys. There were significant increases in smooth muscle actin immunolabeling and collagen staining in these kidneys, relative to the contralateral kidneys. In summary, 90 min of unilateral renal ischemia and delayed contralateral nephrectomy induced histologic and biochemical changes consistent with CKD in cats. A 90-d period between ischemia and nephrectomy resulted in improved survivability of the model.

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