Sakai Hiroyasu, Kurihara Yusuke, Hashimoto Yuki, Chiba Yoshihiko, Misawa Miwa
Department of Pharmacology, School of Pharmacy, Hoshi University, Shinagawa-ku, Tokyo, Japan.
J Smooth Muscle Res. 2010;46(5):259-66. doi: 10.1540/jsmr.46.259.
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.
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。