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丝裂原活化蛋白激酶激酶抑制剂PD 098059对豚鼠气道抗原激发的体外作用

Effects of mitogen-activated protein kinase kinase inhibitor PD 098059 on antigen challenge of guinea-pig airways in vitro.

作者信息

Tsang F, Koh A H, Ting W L, Wong P T, Wong W S

机构信息

Department of Pharmacology, Faculty of Medicine, National University of Singapore, Republic of Singapore.

出版信息

Br J Pharmacol. 1998 Sep;125(1):61-8. doi: 10.1038/sj.bjp.0702049.

DOI:10.1038/sj.bjp.0702049
PMID:9776345
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1565601/
Abstract
  1. It has been shown that activation of protein tyrosine kinases is the earliest detectable signalling response to FcepsilonRI cross-linking on mast cell. Following tyrosine kinase activation, a family of mitogen-activated protein kinases (MAPKs) was found to be activated as well. The present study examined the role of MAPK signalling cascade in in vitro model of allergic asthma using a specific MAPK kinase inhibitor PD 098059. 2. Guinea-pigs were passively sensitized with IgG antibody raised against ovalbumin (OA). Effects of PD 098059 on OA-induced anaphylactic contraction of isolated bronchi and release of histamine and peptidoleukotrienes from chopped lung preparations were studied. 3. PD 098059 (10-50 microM) produced only minor reduction of maximal OA-induced bronchial contraction. In contrast, the rate of relaxation of OA-induced bronchial contraction was markedly faster in the presence of PD 098059 than the vehicle control in a concentration-dependent manner. 4. These observations corroborate well with the inability of PD 098059 (5-50 microM) to substantially block the OA-induced release of histamine and with marked inhibition of OA-induced release of peptidoleukotrienes from lung fragments in the presence of PD 098059. Exogenous arachidonic acid-induced release of peptidoleukotrienes from lung fragments was not blocked by PD 098059. 5. In immunoblotting study, we found that p42MAPK was constitutively expressed in guinea-pig bronchi. However, treatment with OA, histamine or LTD4 did not cause activation of p42MAPK. These findings together with the lack of inhibitory effects of PD 098059 on bronchial contraction induced by histamine or LTD4 suggest that histamine- and LTD4-induced bronchial contractions are not mediated by p42MAPK activation. 6. Taken together, our findings show that inhibition of MAPK signalling cascade by PD 098059 significantly reduced the OA-triggered release of peptidoleukotrienes leading to rapid relaxation of anaphylactic bronchial contraction. On the other hand, p42MAPK did not play a role in histamine- or LTD4-induced bronchial smooth muscle contraction suggesting that PD 098059 exerts its inhibitory effects on OA-induced bronchial contraction primarily through inhibition of peptidoleukotrienes release from mast cells.
摘要
  1. 研究表明,蛋白酪氨酸激酶的激活是肥大细胞上FcepsilonRI交联后最早可检测到的信号反应。酪氨酸激酶激活后,发现有一组丝裂原活化蛋白激酶(MAPKs)也被激活。本研究使用一种特异性的MAPK激酶抑制剂PD 098059,在过敏性哮喘的体外模型中研究了MAPK信号级联的作用。2. 用抗卵清蛋白(OA)的IgG抗体对豚鼠进行被动致敏。研究了PD 098059对OA诱导的离体支气管过敏收缩以及切碎肺组织中组胺和肽白三烯释放的影响。3. PD 098059(10 - 50 microM)仅使OA诱导的最大支气管收缩略有降低。相反,在存在PD 098059的情况下,OA诱导的支气管收缩的松弛速率明显比溶剂对照组快,且呈浓度依赖性。4. 这些观察结果与PD 098059(5 - 50 microM)不能显著阻断OA诱导的组胺释放以及在存在PD 098059时对OA诱导的肺组织片段中肽白三烯释放有明显抑制作用相吻合。外源性花生四烯酸诱导的肺组织片段中肽白三烯的释放未被PD 098059阻断。5. 在免疫印迹研究中,我们发现p42MAPK在豚鼠支气管中组成性表达。然而,用OA、组胺或LTD4处理并未导致p42MAPK的激活。这些发现以及PD 098059对组胺或LTD4诱导的支气管收缩缺乏抑制作用表明,组胺和LTD4诱导的支气管收缩不是由p42MAPK激活介导的。6. 综上所述,我们的研究结果表明,PD 098059对MAPK信号级联的抑制显著降低了OA触发的肽白三烯释放,导致过敏支气管收缩快速松弛。另一方面,p42MAPK在组胺或LTD4诱导的支气管平滑肌收缩中不起作用,这表明PD 098059对OA诱导的支气管收缩的抑制作用主要是通过抑制肥大细胞释放肽白三烯来实现的。