Yoshimura H, Kai T, Nishimura J, Kobayashi S, Takahashi S, Kanaide H
Department of Anesthesiology and Critical Care Medicine, Faculty of Medicine, Kyushu University, Fukuoka, Japan.
Anesthesiology. 1995 Nov;83(5):1009-20. doi: 10.1097/00000542-199511000-00015.
It has been demonstrated that a group of minor tranquilizers, benzodiazepines, are able to relax airway smooth muscles. To determine the underlying mechanisms of this phenomenon, the effects of midazolam on the intracellular Ca2+ concentration ([Ca2+]i) and tension in airway smooth muscles were investigated.
Using front-surface fluorometry and fura-2-loaded porcine tracheal smooth muscle strips, both [Ca2+]i and isometric tension developments were simultaneously recorded.
When the tracheal strips were exposed to a high external K(+)-solution (40 mM) or 10(-7) M carbachol containing 1.25 mM Ca2+, both [Ca2+]i and tension increased rapidly until they reached a plateau (the steady state). During steady-state contraction induced by K(+)-depolarization or carbachol, the cumulative application of midazolam (10(-7) approximately 10(-4) M) caused decreases in both [Ca2+]i and tension, in a concentration-dependent manner. During 40 mM K(+)-induced depolarization, the stepwise increases in the extracellular Ca2+ concentration induced the stepwise increases in [Ca2+]i and tension. Midazolam (3 x 10(-5) M) inhibited these increases in [Ca2+]i and tension, but had no effect on the [Ca2+]i-tension relationship. In the presence of 3 x 10(-3) M NiCl2 (a nonselective cation channel blocker), midazolam (3 x 10(-5) M) did not cause any additional reduction of [Ca2+]i or tension during the contraction induced by carbachol (10(-7) M). In the absence of extracellular Ca2+, midazolam (3 x 10(-5) M) had no effect on the transient increases in either [Ca2+]i or the tension induced by carbachol (10(-7) M) or caffeine (20 mM). Pretreatment with both 10(-5) M flumazenil (a specific central antagonist of benzodiazepines) and 10(-5) M PK11195 (a specific peripheral antagonist of benzodiazepines) did not influence the effect of 10(-5) M midazolam on [Ca2+]i or tension during the contractions induced by carbachol.
Midazolam directly relaxes airway smooth muscles by decreasing [Ca2+]i; this can be attributed to the inhibition of the influx of extracellular Ca2+. Midazolam has no effect on the release of stored Ca2+. In addition, midazolam has no effect on Ca2+ sensitivity of the contractile apparatus. Finally, benzodiazepine antagonists, flumazenil and PK11195, have no effect on this mechanism of direct action of midazolam on airway smooth muscles.
已证实一组弱安定药,即苯二氮䓬类药物,能够舒张气道平滑肌。为确定此现象的潜在机制,研究了咪达唑仑对气道平滑肌细胞内钙离子浓度([Ca2+]i)和张力的影响。
使用表面荧光测定法和负载fura - 2的猪气管平滑肌条,同时记录[Ca2+]i和等长张力变化。
当气管条暴露于高浓度细胞外钾溶液(40 mM)或含1.25 mM Ca2+的10(-7) M卡巴胆碱时,[Ca2+]i和张力均迅速增加直至达到平台期(稳态)。在由钾离子去极化或卡巴胆碱诱导的稳态收缩过程中,累积应用咪达唑仑(10(-7) ~ 10(-4) M)导致[Ca2+]i和张力均以浓度依赖方式降低。在40 mM钾离子诱导的去极化过程中,细胞外钙离子浓度的逐步增加导致[Ca2+]i和张力逐步增加。咪达唑仑(3×10(-5) M)抑制了[Ca2+]i和张力的这些增加,但对[Ca2+]i - 张力关系无影响。在存在3×10(-3) M氯化镍(一种非选择性阳离子通道阻滞剂)的情况下,咪达唑仑(3×10(-5) M)在卡巴胆碱(10(-7) M)诱导的收缩过程中未引起[Ca2+]i或张力的任何额外降低。在无细胞外钙离子的情况下,咪达唑仑(3×10(-5) M)对卡巴胆碱(10(-7) M)或咖啡因(20 mM)诱导的[Ca2+]i或张力的瞬时增加无影响。用10(-5) M氟马西尼(苯二氮䓬类药物的特异性中枢拮抗剂)和10(-5) M PK11195(苯二氮䓬类药物的特异性外周拮抗剂)预处理,不影响10(-5) M咪达唑仑在卡巴胆碱诱导的收缩过程中对[Ca2+]i或张力的作用。
咪达唑仑通过降低[Ca2+]i直接舒张气道平滑肌;这可归因于对细胞外钙离子内流的抑制。咪达唑仑对储存钙离子的释放无影响。此外,咪达唑仑对收缩装置的钙离子敏感性无影响。最后,苯二氮䓬类拮抗剂氟马西尼和PK11195对咪达唑仑对气道平滑肌的这种直接作用机制无影响。