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Comparison of 5 Different Rat Models to Establish a Standard Animal Model for Research Into Interstitial Cystitis

机译:比较5种不同大鼠模型建立标准动物模型研究全术膀胱炎

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摘要

Purpose We evaluated 5 different rat models using different agents in order to establish a standard animal model for interstitial cystitis (IC) in terms of the functional and pathologic characteristics of the bladder. Methods Five IC models were generated in 8-week-old female Sprague-Dawley rats via transurethral instillation of 0.1M hydrogen chloride (HCl) or 3% acetic acid (AA), intraperitoneal injection of cyclophosphamide (CYP) or lipopolysaccharide (LPS), or subcutaneous injection of uroplakin II (UPK2). After generating the IC models, conscious cystometry was performed on days 3, 7, and 14. All rats were euthanized on day 14 and their bladders were obtained for histological and pro-inflammatory-related gene expression analysis. Results In the cystometric analysis, all experimental groups showed significantly decreased intercontraction intervals compared with the control group on day 3, but only the LPS and UPK groups maintained significantly shorter intercontraction intervals than the control group on day 14. The histological analysis revealed that areas with severe urothelial erosion (HCl, AA, and UPK) and hyperplasia (CYP and LPS), particularly in the UPK-treated bladders, showed a markedly increased infiltration of toluidine blue-stained mast cells and increased tissue fibrosis. In addition, significantly elevated expression of interleukin-1b, interleukin-6, myeloperoxidase, monocyte chemotactic protein 1, and Toll-like receptors 2 and 4 was observed in the UPK group compared to the other groups. Conclusions Among the 5 different agents, the injection of UPK generated the most effective IC animal model, showing consequent urothelial barrier loss, inflammatory reaction, tissue fibrosis stimulation, and persistent hyperactive bladder.
机译:目的,我们使用不同剂评估了5种不同的大鼠模型,以便在膀胱功能和病理特征方面为间质膀胱炎(IC)建立标准动物模型。方法在8周龄雌性Sprague-Dawley大鼠中产生5种IC模型,通过经尿道滴注0.1M氯化氢(HCl)或3%乙酸(AA),腹腔注射环磷酰胺(CYP)或脂多糖(LPS),或皮下注射Uroplakin II(UPK2)。在产生IC模型之后,在第3,7和14天进行有意识的囊谱仪。在第14天和所有大鼠安乐死,并获得其膀胱用于组织学和促炎相关的基因表达分析。结果在囊曲线分析中,与第3天相比,所有实验组显示与对照组相比显着降低的间隔,但是在第14天,只有LPS和UPK组比对照组保持明显较短的间隔。组织学分析显示了该地区严重的尿路上侵蚀(HCl,AA和UPK)和增生(CYP和LPS),特别是在UPK处理的膀胱中,表现出显着增加的甲苯胺蓝染色的肥大细胞渗透并增加组织纤维化。另外,与其他基团相比,在UPK组中观察到白细胞介素-1b,白细胞介素-6,髓氧化氢氧化酶,单核细胞趋化蛋白1和1次受体2和4的显着升高。结论在5种不同的药剂中,UPK注射产生最有效的IC动物模型,显示出随后的尿路上移损失,炎症反应,组织纤维化刺激和持续的过度活跃膀胱。

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