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Changes of Colonic Mucosal Microcirculation and Histology in Two Colitis Models: An Experimental Study Using Intravital Microscopy and a New Histological Scoring System

机译:两种结肠炎模型中结肠黏膜微循环和组织学的变化:使用玻璃体内显微镜和新的组织学评分系统进行的实验研究

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This study investigated capillary blood flow (CBF) and pathomorphological alterations in the mucosa of different bowel segments at different times after disease onset in rats with colitis induced by either trinitrobenzensulfonic acid (TNBS) or mitomycin-C. CBF was determined by intravital microscopy using fluorescein-labeled erythrocytes. The histological degree of inflammation was assessed by a new scoring system. Severe acute histological changes were found in the distal colon 24 hr after induction of TNBS colitis (score: 8.9 ± 1.0). CBF was increased (2.9 ± 0.05 vs. 2.6 ± 0.04 nl/min in healthy controls). The histological alterations persisted until day 3 (8.5 ± 0.9) when CBF significantly decreased (1.8 ± 0.05 nl/min). After 15 days, moderate acute inflammation was still detectable histologically (5.4 ± 1.3), but CBF had returned to normal values. In mitomycin-C colitis, changes developed mainly in the proximal colon: After three days, there was mild inflammation (2.8 ± 1.2) with normal CBF (2.5 ± 0.1 nl/min). After seven days, the inflammation had increased (4.8 ± 1.1), while CBF had decreased (1.5 ± 0.06 nl/min). These changes persisted for six weeks (5.3 ± 0.7; 1.2 ± 0.05 nl/min). These data suggest that disturbed colonic microcirculation may play an important role in the pathogenesis of inflammatory bowel disease regardless of the histopathomorphological alterations.
机译:这项研究调查了三硝基苯磺酸(TNBS)或丝裂霉素C诱发的结肠炎大鼠在疾病发作后不同时间在不同肠段粘膜的毛细血管血流量(CBF)和病理形态学变化。使用荧光素标记的红细胞通过活体显微镜检查确定CBF。通过新的评分系统评估炎症的组织学程度。 TNBS结肠炎诱发后24小时,在远端结肠中发现了严重的急性组织学改变(评分:8.9±1.0)。 CBF增加(健康对照组为2.9±0.05 vs. 2.6±0.04 nl / min)。组织学改变一直持续到第3天(8.5±0.9),此时CBF明显降低(1.8±0.05 nl / min)。 15天后,组织学上仍可检测到中度急性炎症(5.4±1.3),但脑血流量已恢复正常。在丝裂霉素C结肠炎中,变化主要发生在近端结肠:三天后,CBF正常(2.5±0.1 nl / min)出现轻度炎症(2.8±1.2)。 7天后,炎症增加(4.8±1.1),而CBF减少(1.5±0.06 nl / min)。这些变化持续了六周(5.3±0.7; 1.2±0.05 nl / min)。这些数据表明,无论组织病理形态学改变如何,结肠结肠微循环障碍可能在炎症性肠病的发病机理中起重要作用。

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