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Dexamethasone inhibition of leucocyte adhesion to rat mesenteric postcapillary venules: role of intercellular adhesion molecule 1 and KC

机译:地塞米松抑制白细胞粘附于大鼠肠系膜毛细血管后小静脉:细胞间粘附分子1和KC的作用

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摘要

BACKGROUND—A previous study showed that the glucocorticoid dexamethasone, at doses of 100 µg/kg and above, inhibited leucocyte adhesion to rat mesenteric postcapillary venules activated with interleukin 1β (IL-1β), as assessed by videomicroscopy.
AIMS—To identify whether the adhesion molecule, intercellular adhesion molecule 1 (ICAM-1), or the chemokine KC could be targeted by the steroid to mediate its antiadhesive effect.
METHODS—Rat mesenteries were treated with IL-1β (20 ng intraperitoneally) and the extent of leucocyte adhesion measured at two and four hours using intravital microscopy. Rats were treated with dexamethasone, and passively immunised against ICAM-1 or KC. Endogenous expression of these two mediators was validated by immunohistochemistry, ELISA, and the injection of specific radiolabelled antibodies.
RESULTS—Dexamethasone greatly reduced IL-1β induced leucocyte adhesion, endothelial expression of ICAM-1 in the postcapillary venule, and release of the mast cell derived chemokine KC. Injection of specific antibodies to the latter mediators was also extremely effective in downregulating (>80%) IL-1β induced leucocyte adhesion.
CONCLUSIONS—Induction by IL-1β of endogenous ICAM-1 and KC contributes to leucocyte adhesion to inflamed mesenteric vessels. Without excluding other possible mediators, these data clearly show that dexamethasone interferes with ICAM-1 expression and KC release from mast cells, resulting in suppression of leucocyte accumulation in the bowel wall, which is a prominent feature of several gastrointestinal pathologies.


Keywords: inflammation; glucocorticoids; intravital microscopy; mast cell; neutrophil; endothelium
机译:背景技术–先前的研究表明,糖皮质激素地塞米松的剂量大于或等于100 µg / kg,如通过视频显微镜评估的那样,可抑制白细胞粘附于被白介素1β(IL-1β)激活的大鼠肠系膜后毛细血管。
AIMS-为了确定类固醇是否可以靶向粘附分子,细胞间粘附分子1(ICAM-1)或趋化因子KC介导其抗粘附作用。
方法-用IL-1β(20ng腹膜内),并在2和4小时内使用活体显微镜测量白细胞粘附程度。用地塞米松治疗大鼠,并被动免疫ICAM-1或KC。通过免疫组织化学,ELISA和注射特异性放射性标记的抗体验证了这两种介体的内源性表达。
结果—地塞米松极大地降低了IL-1β诱导的白细胞粘附,毛细血管后小静脉中ICAM-1的内皮表达并释放肥大细胞衍生的趋化因子KC。向后一种介质注射特异性抗体在下调(> 80%)IL-1β诱导的白细胞粘附方面也非常有效。
结论—IL-1β诱导内源性ICAM-1和KC导致白细胞粘附导致发炎肠系膜血管。在不排除其他可能介质的情况下,这些数据清楚地表明地塞米松会干扰肥大细胞中ICAM-1的表达和KC释放,从而抑制白细胞在肠壁中的蓄积,这是几种胃肠道病理学的突出特征。


关键词:炎症;糖皮质激素;活体显微镜检查肥大细胞中性粒细胞内皮细胞

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