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Influence of erythrocyte function-enhancing drugs on the bronchoprotective actions of chemokine receptor blockers in mice

机译:增强红细胞功能的药物对趋化因子受体阻滞剂对小鼠支气管保护作用的影响

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Background:CC chemokine receptors are likely to have important roles in the regulation of leukocytes and mast cells. Chemokine receptors are crucial in orchestrating innate and acquired immune responses as well as in allergic inflammation. A disturbance in erythrocyte function can lead to bronchial hyperreactivity and asthma.Material/Methods:This study was conducted on Swiss albino mice weighing between 25 to 35 g. The animals were divided into eight groups (n=8). Groups of mice (n=8) were pretreated with the chemokine receptor blockers A122058 (600 μg/kg i.p.) or cyclophosphamide (20 mg/kg i.p.). Other groups received A122058 or cyclophosphamide in combination with either erythropoietin and quercetin. The effects of these drugs on bronchoconstriction and salivation induced by carbachol were evaluated.Results:The results of this study suggest that blockade of chemokine receptors significantly potentiated erythropoietin- and quercetin-induced inhibition of carbachol-induced bronchoconstriction ([i]P[/i]0.05).Conclusions:The results of this study suggest that blockade of chemokine receptors and enhancement of the erythrocyte function together potentiate the bronchoprotective effects of these drugs. This combination could be a novel strategy in combating bronchial hyper-responsiveness.
机译:背景:CC趋化因子受体可能在白细胞和肥大细胞的调节中起重要作用。趋化因子受体在协调先天和后天免疫应答以及过敏性炎症中至关重要。红细胞功能紊乱可导致支气管高反应性和哮喘。材料/方法:这项研究是针对体重在25至35 g之间的瑞士白化病小鼠进行的。将动物分为八组(n = 8)。用趋化因子受体阻滞剂A122058(600μg/ kg腹腔内)或环磷酰胺(20 mg / kg腹腔内)对每组小鼠(n = 8)进行预处理。其他组接受A122058或环磷酰胺联合促红细胞生成素和槲皮素。结果:这项研究的结果表明,趋化因子受体的阻断显着增强了促红细胞生成素和槲皮素诱导的对胆碱引起的支气管收缩的抑制作用[iP [/ i] [0.05]。结论:这项研究的结果表明,趋化因子受体的阻断和红细胞功能的增强共同增强了这些药物的支气管保护作用。这种组合可能是对抗支气管高反应性的新策略。

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