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首页> 外文期刊>British Journal of Pharmacology >β_2-adrenoceptor agonists inhibit release of eosinophil-activating cytokines from human airway smooth muscle cells
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β_2-adrenoceptor agonists inhibit release of eosinophil-activating cytokines from human airway smooth muscle cells

机译:β_2-肾上腺素受体激动剂抑制人气道平滑肌细胞释放嗜酸性粒细胞激活的细胞因子

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摘要

Airway smooth muscle(ASM)is a potential source of multiple pro-inflammatory cytokines during airway inflammation.β-Adrenoceptor agonist hyporesponsiveness is a characteristic feature of asthma, and interleukin(IL)-1βand tumour necrosis factor(TNF)-αare implicated in its cause. Here, the capacity ofβ-adrenoceptor agonists to prevent release of GM-CSF, RANTES, eotaxin and IL-8, elicited by IL-1βor TNF-α, was examined in human ASM cells. Isoprenaline(~EC_50 150 nM), a non-selectiveβ-adrenoceptor agonist, and salbutnmol(~EC_50 25 nM), a selectiveβ_2-adrenoceptor agonist, attenuated release of GM-CSF, RANTES and eotaxin, but not IL-8(EC_50 > 1μM).
机译:气道平滑肌(ASM)是气道炎症过程中多种促炎细胞因子的潜在来源。β-肾上腺素受体激动剂反应低下是哮喘的特征,白介素(IL)-1β和肿瘤坏死因子(TNF)-α参与其中。原因。在此,在人ASM细胞中检查了β-肾上腺素受体激动剂阻止由IL-1β或TNF-α引起的GM-CSF,RANTES,嗜酸性粒细胞趋化因子和IL-8释放的能力。异丙肾上腺素(〜EC_50 150 nM)是一种非选择性β-肾上腺素受体激动剂,而沙丁胺醇(〜EC_50 25 nM)是一种选择性β_2-肾上腺素受体激动剂,减缓了GM-CSF,RANTES和嗜酸性粒细胞趋化因子的释放,但对IL-8的释放不佳(EC_50> 1μM)。

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