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增强型佛波醇丁酯介导的抗原诱导气道高反应性小鼠支气管平滑肌收缩。

Augmented PDBu-mediated contraction of bronchial smooth muscle of mice with antigen-induced airway hyperresponsiveness.

作者信息

Sakai Hiroyasu, Kurihara Yusuke, Hashimoto Yuki, Chiba Yoshihiko, Misawa Miwa

机构信息

Department of Pharmacology, School of Pharmacy, Hoshi University, Shinagawa-ku, Tokyo, Japan.

出版信息

J Smooth Muscle Res. 2010;46(5):259-66. doi: 10.1540/jsmr.46.259.

Abstract

To explore the role of protein kinase C (PKC) in the augmented bronchial smooth muscle (BSM) contraction observed in the antigen-induced airway hyperresponsive (AHR) mice, the effects of a PKC activator, phorbol 12,13-dibutylate (PDBu), on BSM contraction were compared between the AHR and control mice. Actively sensitized mice were repeatedly challenged by antigen inhalation. Twenty-four hours after the final antigen challenge the isometrical contractions of the BSMs were measured. The BSM contraction induced by acetylcholine, but not high K(+) depolarization, was significantly augmented in the AHR mice. In BSMs of control mice, PDBu caused a significant increase in tension when the tissues were precontracted with high K(+), although PDBu itself had no effect on basal tone. The PDBu-mediated contraction was markedly augmented in BSMs of the AHR mice. These findings suggest that an increase in the PKC-mediated signaling is involved in the augmented contraction of BSMs in the antigen-induced AHR mice.

摘要

为了探究蛋白激酶C(PKC)在抗原诱导的气道高反应性(AHR)小鼠中观察到的支气管平滑肌(BSM)收缩增强中的作用,比较了PKC激活剂佛波醇12,13 - 二丁酯(PDBu)对AHR小鼠和对照小鼠BSM收缩的影响。主动致敏的小鼠通过吸入抗原反复激发。在最后一次抗原激发后24小时,测量BSM的等长收缩。乙酰胆碱诱导的BSM收缩在AHR小鼠中显著增强,但高钾(K⁺)去极化诱导的收缩未增强。在对照小鼠的BSM中,当组织用高钾预收缩时,PDBu导致张力显著增加,尽管PDBu本身对基础张力没有影响。PDBu介导的收缩在AHR小鼠的BSM中明显增强。这些发现表明,PKC介导的信号传导增加参与了抗原诱导的AHR小鼠中BSM收缩的增强。

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