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蜂毒明肽敏感钾通道参与豚鼠离体气管抗原诱导的痉挛

Involvement of apamin-sensitive K+ channels in antigen-induced spasm of guinea-pig isolated trachea.

作者信息

Yamauchi H, Miura M, Ichinose M, Ishikawa J, Nakajima N, Tomaki M, Inoue H, Maeyama K, Watanabe T, Shirato K

机构信息

First Department of Internal Medicine, Tohoku University School of Medicine, Sendai, Japan.

出版信息

Br J Pharmacol. 1994 Jul;112(3):958-62. doi: 10.1111/j.1476-5381.1994.tb13174.x.

Abstract
  1. In order to examine whether K+ channels play a role in antigen-induced airway responses, the effect of K+ channel blockers on antigen-induced airway smooth muscle contraction and mediator release was examined in vitro in guinea-pigs actively sensitized with ovalbumin (OA). 2. Tracheal strips from sensitized animals were suspended in organ baths under a resting tension of 1 g and isometric tension was continuously measured. Cumulative concentration-response curves to OA (0.1-1000 ng ml-1) or histamine (10 nM-1 mM) were obtained in the presence and absence of K+ channel blockers. 3. OA (10, 100 or 1000 ng ml-1) was incubated with minced lung tissues from the same animals for 15 min in the presence and absence of K+ channel blockers, and released histamine and leukotriene C4 (LTC4) in the incubating medium were measured. 4. Apamin, a small conductance Ca(2+)-activated K+ channel (PK,Ca) blocker, (0.1, 0.3 and 1 microM) significantly inhibited OA-induced smooth muscle contraction, while charybdotoxin (ChTX, 10 nM), an intermediate and large conductance PK,Ca blocker, and iberiotoxin (IbTX, 3 nM), a large conductance PK,Ca blocker, were without effect. Apamin (0.3 microM) had no effect on exogenously administered histamine-induced airway smooth muscle contraction, suggesting that the inhibition of OA-induced contraction by apamin did not occur at the smooth muscle level. 5. The inhibition of OA-induced contraction by apamin (0.3 microM) was not significantly affected by pretreatment with a leukotriene antagonist, ONO-1078 (10 microM), but was abolished by pretreatment with a histamine H1-receptor blocker, pyrilamine (1 microM). 6. Apamin by itself (up to 0.1 MicroM) had no effect on spontaneous histamine release from minced lung tissues. Histamine release induced by low and intermediate concentrations of OA (10 and 100 ng ml-1)was significantly suppressed by apamin pretreatment (P<0.05 and P<0.001), whereas LTC4 release was not affected. ChTX (0.1 MicroM) and IbTX (10 nM) had no significant effect on either spontaneous or OA (100 ng ml-1)-induced histamine release.7. These results suggest that apamin partially but substantially inhibits antigen-induced smooth muscle contraction, presumably by inhibiting antigen-induced histamine release from airway mast cells through small conductance PKca closure.
摘要
  1. 为了研究钾离子通道是否在抗原诱导的气道反应中发挥作用,我们在体外检测了钾离子通道阻滞剂对卵清蛋白(OA)主动致敏的豚鼠抗原诱导的气道平滑肌收缩和介质释放的影响。2. 将致敏动物的气管条悬挂于器官浴槽中,静息张力为1 g,并持续测量等长张力。在存在和不存在钾离子通道阻滞剂的情况下,获得对OA(0.1 - 1000 ng/ml)或组胺(10 nM - 1 mM)的累积浓度 - 反应曲线。3. 在存在和不存在钾离子通道阻滞剂的情况下,将OA(10、100或1000 ng/ml)与来自同一动物的肺组织匀浆孵育15分钟,并测量孵育介质中释放的组胺和白三烯C4(LTC4)。4. 蜂毒明肽,一种小电导钙激活钾通道(PK,Ca)阻滞剂,(0.1、0.3和1 μM)显著抑制OA诱导的平滑肌收缩,而中间电导和大电导PK,Ca阻滞剂蝎毒素(ChTX,10 nM)和大电导PK,Ca阻滞剂iberiotoxin(IbTX,3 nM)则无作用。蜂毒明肽(0.3 μM)对外源性给予组胺诱导的气道平滑肌收缩无影响,这表明蜂毒明肽对OA诱导的收缩的抑制作用不是在平滑肌水平发生的。5. 蜂毒明肽(0.3 μM)对OA诱导的收缩的抑制作用不受白三烯拮抗剂ONO - 1078(10 μM)预处理的显著影响,但被组胺H1受体阻滞剂吡苄明(1 μM)预处理所消除。6. 蜂毒明肽本身(高达0.1 μM)对肺组织匀浆中组胺的自发释放无影响。低浓度和中等浓度OA(10和100 ng/ml)诱导的组胺释放被蜂毒明肽预处理显著抑制(P < 0.05和P < 0.001),而LTC4释放不受影响。ChTX(0.1 μM)和IbTX(10 nM)对自发或OA(100 ng/ml)诱导的组胺释放均无显著影响。7. 这些结果表明,蜂毒明肽部分但显著地抑制抗原诱导的平滑肌收缩,推测是通过关闭小电导PKca抑制气道肥大细胞中抗原诱导的组胺释放。

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