孟鲁卡斯特
卵清蛋白
白三烯
药理学
白三烯受体
甲基强的松龙
白三烯D4
敌手
化学
扎尔鲁卡斯特
体内
哮喘
受体拮抗剂
受体
白三烯C4
体外
细胞浸润
免疫学
医学
内科学
炎症
生物
生物化学
免疫系统
生物技术
作者
Akira Murai,Masayoshi Abe,Yuri Hayashi,Noriyuki Sakata,Takeshi Katsuragi,Kéiichi Tanaka
标识
DOI:10.1124/jpet.104.074922
摘要
We investigated the effects of cysteinyl-leukotriene (cysLT) type 1 receptor antagonist montelukast (MK) and compared them with those of methylprednisolone (MP) in an allergic asthma model. Rats sensitized to ovalbumin (OVA) received repeated intratracheal exposure to OVA for up to 3 consecutive days. Pretreatment with MK or MP before OVA exposure inhibited late airway response (LAR) and reduced cellular infiltration into the bronchial submucosa after the triple OVA. The amount of N-acetyl-leukotriene E4 in the bile was significantly reduced by pretreatment with MK or MP, suggesting that both drugs reduced the production of cysLTs in the lungs. In the in vitro study, when the fragments of lungs that had been repeatedly pretreated with MK or MP and exposed to OVA were removed and incubated with OVA, the coaddition of either drug significantly reduced cysLT production. In contrast, the cysLT production following the addition of OVA to the lung fragments that had not received in vivo pretreatment with either drug was inhibited by MK but not by MP. These results indicate that MK and MP inhibit LAR by suppressing the infiltration of inflammatory cells into the bronchial submucosa, thereby inhibiting the production of cysLTs in the lungs, and that MK but not MP may inhibit cysLT production directly. The different effects on cysLT production between the two drugs may provide a rationale for the use of combination therapy with cysLT1 receptor antagonists and steroids for the treatment of asthma.
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