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Effects of Acute and Chronic Exposure to Residual Level Erythromycin on Human Intestinal Epithelium Cell Permeability and Cytotoxicity

机译:急性和慢性暴露于残余水平的红霉素对人肠上皮细胞通透性和细胞毒性的影响

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摘要

Residual concentrations of erythromycin in food could result in gastrointestinal tract exposure that potentially poses a health-hazard to the consumer, affecting intestinal epithelial permeability, barrier function, microbiota composition, and antimicrobial resistance. We investigated the effects of erythromycin after acute (48 h single treatment with 0.03 μg/mL to 300 μg/mL) or chronic (repeated treatment with 0.3 µg/mL and 300 µg/mL erythromycin for five days) exposures on the permeability of human colonic epithelial cells, a model that mimics a susceptible intestinal surface devoid of commensal microbiota. Transepithelial electrical resistance (TER) measurements indicated that erythromycin above 0.3 µg/mL may compromise the epithelial barrier. Acute exposure increased cytotoxicity, while chronic exposure decreased the cytotoxicity. Quantitative PCR analysis revealed that only ICAM1 (intercellular adhesion molecule 1) was up-regulated during 0.3 μg/mL acute-exposure, while ICAM1, JAM3 (junctional adhesion molecule 3), and ITGA8 (integrin alpha 8), were over-expressed in the 300 μg/mL acute treatment group. However, during chronic exposure, no change in the mRNA expression was observed at 0.3 μg/mL, and only ICAM2 was significantly up-regulated after 300 μg/mL. ICAM1 and ICAM2 are known to be involved in the formation of extracellular matrices. These gene expression changes may be related to the immunoregulatory activity of erythromycin, or a compensatory mechanism of the epithelial cells to overcome the distress caused by erythromycin due to increased permeability.
机译:食物中残留的红霉素浓度可能会导致胃肠道暴露,从而可能对消费者造成健康危害,从而影响肠道上皮的渗透性,屏障功能,微生物群组成和抗菌素耐药性。我们研究了急性暴露(0.03μg/ mL至300μg/ mL的单次治疗48小时)或慢性暴露(0.3μg/ mL和300μg/ mL的红霉素重复治疗5天)对人体通透性的影响。结肠上皮细胞,一种模拟没有共生菌群的敏感肠道表面的模型。经上皮电阻(TER)测量表明,红霉素超过0.3 µg / mL可能会损害上皮屏障。急性暴露会增加细胞毒性,而慢性暴露会降低细胞毒性。定量PCR分析显示,在0.3μg/ mL急性暴露过程中,仅ICAM1(细胞间粘附分子1)被上调,而ICAM1,JAM3(连接粘附分子3)和ITGA8(整合素α8)在ICAM1中过表达。 300μg/ mL急性治疗组。但是,在长期暴露期间,在0.3μg/ mL下未观察到mRNA表达的变化,在300μg/ mL后仅ICAM2显着上调。已知ICAM1和ICAM2参与细胞外基质的形成。这些基因表达的变化可能与红霉素的免疫调节活性有关,或者与上皮细胞克服由于增加的通透性而引起的由红霉素引起的困扰的补偿机制有关。

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