Department of Pediatrics Louisiana State University Medical Center New Orleans LA USA.
Mediators Inflamm. 1995;4(1):19-24. doi: 10.1155/S0962935195000044.
We sought to establish a model of inflammatory bowel disease by augmenting the activity of the local immune system with Freund's complete adjuvant, and to determine if inducible nitric oxide synthase (iNOS) expression and peroxynitrite formation accompanied the inflammatory condition. In anaesthetized guinea-pigs, a loop of distal ileum received intraluminal 50% ethanol followed by Freund's complete adjuvant. Control animals were sham operated. When the animals were killed 7 or 14 days later, loop lavage fluid was examined for nitrite and PGE(2) levels; mucosal levels of granulocyte and macrophages were estimated by myeloperoxidase (MPO) and N-acetyl-D-glucosaminidase (NAG) activity, respectively. Cellular localization if iNOS and peroxynitrite formation were determined by immunohistochemistry with polyclonal antibodies directed against peptide epitopes of mouse iNOS and nitrotyrosine, respectfully. Adjuvant administration resulted in a persistent ileitis, featuring gut thickening, crypt hyperplasia, villus tip swelling and disruption, and cellular infiltration. Lavage levels of PGE(2) and nitrite were markedly elevated by adjuvant treatment. Immunoreactive iNOS and nitrotyrosine bordered on detectability in normal animals but were markedly evident with adjuvant treatment at day 7 and particularly day 14. Immunohistochemistry suggested that enteric neurons and epithelia were major sites of iNOS activity and peroxynitrite formation. We conclude that local administration of adjuvant establishes a chronic ileitis. Inducible nitric oxide synthase may contribute to the inflammatory process.
我们试图通过福氏完全佐剂增强局部免疫系统的活性来建立炎症性肠病模型,并确定诱导型一氧化氮合酶 (iNOS) 的表达和过氧亚硝酸盐的形成是否伴随着炎症状态。在麻醉的豚鼠中,回肠远端环接受腔内 50%乙醇,然后接受福氏完全佐剂。对照动物进行假手术。当动物在 7 或 14 天后被杀死时,检查环灌洗液中的亚硝酸盐和 PGE(2) 水平;通过髓过氧化物酶 (MPO) 和 N-乙酰-D-氨基葡萄糖苷酶 (NAG) 活性分别估计粘膜中粒细胞和巨噬细胞的水平。通过针对小鼠 iNOS 和硝基酪氨酸的肽表位的多克隆抗体的免疫组织化学确定 iNOS 和过氧亚硝酸盐形成的细胞定位。佐剂给药导致持续性回肠炎,其特征为肠道增厚、隐窝增生、绒毛尖端肿胀和破坏以及细胞浸润。佐剂处理后,灌洗液中的 PGE(2) 和亚硝酸盐水平明显升高。在正常动物中,免疫反应性 iNOS 和硝基酪氨酸接近可检测水平,但在佐剂处理的第 7 天和特别是第 14 天明显可见。免疫组织化学表明,肠神经元和上皮是 iNOS 活性和过氧亚硝酸盐形成的主要部位。我们得出结论,局部给予佐剂可建立慢性回肠炎。诱导型一氧化氮合酶可能有助于炎症过程。