rho相关蛋白激酶和组胺在溶血磷脂酸诱导豚鼠气道高反应性中的作用。

T. Hashimoto, Yuuki Nakano, M. Yamashita, Yang-Il Fang, H. Ohata, K. Momose
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引用次数: 26

摘要

吸入油基溶血磷脂酸(LPA)诱导气道对乙酰胆碱(ACh)的高反应性。相反,棕榈酰和硬脂酰LPA的作用最小。吸入rho相关蛋白激酶(ROCK)抑制剂Y-27632可抑制气道高反应性。H1组胺受体拮抗剂甲皮拉米和组胺释放抑制剂、H1组胺受体拮抗剂酮替芬也能抑制LPA诱导的气道高反应性;然而,阿司匹林未能减弱这种反应。肺碎片与LPA孵育引起组胺释放。另一方面,LPA对乙酰胆碱引起的平滑肌收缩无明显影响。这些发现表明,lpa诱导的气道高反应性可归因于Rho/ rock介导的途径通过内皮细胞分化基因(EDG)受体激活,可能是EDG 7。此外,组胺释放也可能参与其中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of Rho-associated protein kinase and histamine in lysophosphatidic acid-induced airway hyperresponsiveness in guinea pigs.
Inhalation of oleoyl lysophosphatidic acid (LPA) induced airway hyperresponsiveness to acetylcholine (ACh). In contrast, palmitoyl and stearoyl LPA exerted minimal effects. Airway hyperresponsiveness was inhibited by inhalation of Y-27632, an inhibitor of Rho-associated protein kinase (ROCK). Mepyramine, an H1 histamine receptor antagonist and ketotifen, an inhibitor of histamine release and H1 histamine receptor antagonist, also inhibited airway hyperresponsiveness induced by LPA; however, aspirin failed to attenuate this response. The incubation of lung fragments with LPA gave rise to releases in histamine. On the other hand, LPA produced no significant changes on the smooth muscle contraction evoked by ACh. These findings suggest that LPA-induced airway hyperresponsiveness is attributable to activation of the Rho/ROCK-mediated pathway via endothelial cell differentiation gene (EDG) receptors, probably EDG 7. Moreover, histamine release may be involved.
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