Departamento de Morfologia-Faculdade de Medicina da Universidade Federal do Ceará, Rua Delmiro de Farias, sn-CEP 60.416-030, Fortaleza, Ceará, Brazil.
Infect Immun. 2011 Feb;79(2):653-62. doi: 10.1128/IAI.01159-10. Epub 2010 Nov 29.
Toxin A (TxA) is able to induce most of the classical features of Clostridium difficile-associated disease in animal models. The objective of this study was to determine the effect of an inhibitor of adenosine deaminase, EHNA [erythro-9-(2-hydroxy-3-nonyl)-adenine], on TxA-induced enteritis in C57BL6 mice and on the gene expression of adenosine receptors. EHNA (90 μmol/kg) or phosphate-buffered saline (PBS) was injected intraperitoneally (i.p.) 30 min prior to TxA (50 μg) or PBS injection into the ileal loop. A(2A) adenosine receptor agonist (ATL313; 5 nM) was injected in the ileal loop immediately before TxA (50 μg) in mice pretreated with EHNA. The animals were euthanized 3 h later. The changes in the tissue were assessed by the evaluation of ileal loop weight/length and secretion volume/length ratios, histological analysis, myeloperoxidase assay (MPO), the local expression of inducible nitric oxide synthase (NOS2), pentraxin 3 (PTX3), NF-κB, tumor necrosis factor alpha (TNF-α), and interleukin-1β (IL-1β) by immunohistochemistry and/or quantitative reverse transcription-PCR (qRT-PCR). The gene expression profiles of A₁, A(2A), A(2B), and A₃ adenosine receptors also were evaluated by qRT-PCR. Adenosine deaminase inhibition, by EHNA, reduced tissue injury, neutrophil infiltration, and the levels of proinflammatory cytokines (TNF-α and IL-1β) as well as the expression of NOS2, NF-κB, and PTX3 in the ileum of mice injected with TxA. ATL313 had no additional effect on EHNA action. TxA increased the gene expression of A₁ and A(2A) adenosine receptors. Our findings show that the inhibition of adenosine deaminase by EHNA can prevent Clostridium difficile TxA-induced damage and inflammation possibly through the A(2A) adenosine receptor, suggesting that the modulation of adenosine/adenosine deaminase represents an important tool in the management of C. difficile-induced disease.
毒素 A (TxA) 能够在动物模型中诱导大多数与艰难梭菌相关的疾病的典型特征。本研究的目的是确定腺苷脱氨酶抑制剂 EHNA [赤式-9-(2-羟基-3-壬基)-腺嘌呤] 对 C57BL6 小鼠 TxA 诱导的肠炎和腺苷受体基因表达的影响。EHNA(90 μmol/kg)或磷酸盐缓冲盐水 (PBS) 在 TxA(50 μg)或 PBS 注射到回肠袢之前 30 分钟经腹腔注射 (i.p.)。在预先用 EHNA 处理的小鼠中,在 TxA(50 μg)之前立即将 A₂A 腺苷受体激动剂 (ATL313; 5 nM) 注入回肠袢。3 小时后处死动物。通过评估回肠袢重量/长度和分泌量/长度比、组织学分析、髓过氧化物酶测定 (MPO)、诱导型一氧化氮合酶 (NOS2)、五聚素 3 (PTX3)、核因子-κB (NF-κB) 、肿瘤坏死因子-α (TNF-α) 和白细胞介素-1β (IL-1β) 的局部表达,评估组织变化 通过免疫组织化学和/或定量逆转录聚合酶链反应 (qRT-PCR)。通过 qRT-PCR 还评估了 A₁、A(2A)、A(2B) 和 A₃ 腺苷受体的基因表达谱。EHNA 通过抑制腺苷脱氨酶,减少了 TxA 注射小鼠回肠中的组织损伤、中性粒细胞浸润和促炎细胞因子 (TNF-α 和 IL-1β) 水平,以及 NOS2、NF-κB 和 PTX3 的表达。ATL313 对 EHNA 的作用没有额外影响。TxA 增加了 A₁ 和 A(2A) 腺苷受体的基因表达。我们的研究结果表明,EHNA 通过抑制腺苷脱氨酶可以预防艰难梭菌 TxA 诱导的损伤和炎症,可能是通过 A(2A) 腺苷受体,提示腺苷/腺苷脱氨酶的调节可能是艰难梭菌诱导疾病管理的重要工具。