Kosaka Junko, Lankadeva Yugeesh R, May Clive N, Bellomo Rinaldo
1Florey Institute of Neuroscience and Mental Health, Melbourne, VIC, Australia.2Department of Intensive Care, Austin Hospital, Melbourne, VIC, Australia.
Crit Care Med. 2016 Sep;44(9):e897-903. doi: 10.1097/CCM.0000000000001735.
The histopathologic changes associated with septic acute kidney injury are poorly understood, in part, because of the lack of biopsy data in humans. Animal models of septic acute kidney injury may help define such changes. Therefore, we performed a systematic review of the histopathologic changes found in modern experimental septic acute kidney injury models.
MEDLINE, EMBASE, Cumulative Index to Nursing and Allied Health Literature, and PubMed (from January 2007 to February 2015).
We reviewed experimental studies reporting findings on the histopathology of contemporary experimental septic acute kidney injury.
We focused on the presence or the absence of acute tubular necrosis, tubular cell apoptosis, and other nonspecific findings.
We identified 102 studies in 1,059 animals. Among the 1,059 animals, 53 (5.0%) did not have any renal histopathologic changes, but acute tubular necrosis was found in 184 (17.4%). The prevalence of acute tubular necrosis was not related to animal size or model of sepsis and was only found in models with low cardiac output and decreased renal blood flow (p < 0.0001). Only 21 studies (170 animals) assessed the prevalence of tubular cell apoptosis, which was reported in 158 animals (92.9%). The prevalence of tubular cell apoptosis was significantly higher in studies using small animals (p < 0.0001) and in peritonitis models (p < 0.0001). Simultaneous acute tubular necrosis and tubular cell apoptosis was rare (55 animals [32.4%]) and only seen with decreased cardiac output and renal blood flow. Nonspecific changes (vacuolization of tubular cells, loss of brush border, and tubular cell swelling) were each observed in 423 (39.9%), 250 (23.6%) and 243 (22.9%) animals, respectively.
In models of experimental septic acute kidney injury in contemporary articles, acute tubular necrosis was relatively uncommon and, when present, reflected the presence of an associated low cardiac output or low renal blood flow syndrome. Tubular cell apoptosis seemed frequent in the few studies in which it was investigated. Nonspecific morphologic changes, however, were the most common histopathologic findings.
与脓毒症急性肾损伤相关的组织病理学变化尚未完全明确,部分原因是缺乏人类活检数据。脓毒症急性肾损伤的动物模型可能有助于明确此类变化。因此,我们对现代实验性脓毒症急性肾损伤模型中的组织病理学变化进行了系统评价。
MEDLINE、EMBASE、护理学与健康相关文献累积索引以及PubMed(2007年1月至2015年2月)。
我们回顾了报告当代实验性脓毒症急性肾损伤组织病理学研究结果的实验性研究。
我们重点关注急性肾小管坏死、肾小管细胞凋亡的有无以及其他非特异性表现。
我们在1059只动物中确定了102项研究。在这1059只动物中,53只(5.0%)没有任何肾脏组织病理学变化,但184只(17.4%)发现有急性肾小管坏死。急性肾小管坏死的发生率与动物大小或脓毒症模型无关,仅在低心输出量和肾血流量减少的模型中出现(p<0.0001)。只有21项研究(170只动物)评估了肾小管细胞凋亡的发生率,其中158只动物(92.9%)报告有肾小管细胞凋亡。在使用小动物的研究(p<0.0001)和腹膜炎模型(p<0.000)中,肾小管细胞凋亡的发生率显著更高。急性肾小管坏死和肾小管细胞凋亡同时出现的情况很少见(55只动物[32.4%]),且仅在伴有心输出量和肾血流量减少时出现。非特异性变化(肾小管细胞空泡化、刷状缘缺失和肾小管细胞肿胀)分别在423只(39.9%)、250只(23.6%)和243只(22.9%)动物中观察到。
在当代文章中的实验性脓毒症急性肾损伤模型中,急性肾小管坏死相对少见,一旦出现,则提示存在相关的低心输出量或低肾血流量综合征。在少数几项研究中,肾小管细胞凋亡似乎很常见。然而,非特异性形态学变化是最常见的组织病理学表现。