Koga Y, Sato S, Sodeyama N, Takahashi M, Kato M, Iwatsuki N, Hashimoto Y
Department of Anesthesiology, Tohoku University School of Medicine, Sendai, Japan.
Br J Anaesth. 1992 Jul;69(1):65-9. doi: 10.1093/bja/69.1.65.
The mechanisms by which benzodiazepines produce muscle relaxation and respiratory depression are not known, but they may include actions on peripheral benzodiazepine receptors or central GABA receptors, or a direct action on airway smooth muscle may also be involved. We have compared, therefore, the effects of diazepam, flunitrazepam and midazolam on airway tone by measuring isometric tension of guineapig trachealis muscle. Cumulative concentrations of diazepam, flunitrazepam and midazolam caused concentration-dependent relaxation of resting tone in the tracheal smooth muscle with no significant differences in pD2 values (-log EC50--an index of potency) or intrinsic activities (% of maximum response) for relaxations for the three compounds. Pretreatment with propranolol 10(-6) mol litre-1, flumazenil 10(-7) and 10(-6) mol litre-1 or PK11195 10(-6) mol litre-1 had no effect on diazepam- or midazolam-induced relaxation. Diazepam 3 x 10(-6) mol litre-1 pretreatment shifted the concentration-response curves for acetylcholine, histamine and serotonin (5-HT) to the right by a factor of approximately 2. Flunitrazepam 3 x 10(-6) mol litre-1 pretreatment also shifted the curves for histamine and 5-HT similarly to the right, whereas midazolam pretreatment did not inhibit any agonist-induced contractions. These results suggest that benzodiazepines relax airway smooth muscle, not via neural pathways or central and peripheral benzodiazepine receptors, but by a direct action on airway smooth muscle.
苯二氮䓬类药物产生肌肉松弛和呼吸抑制的机制尚不清楚,但可能包括作用于外周苯二氮䓬受体或中枢γ-氨基丁酸(GABA)受体,也可能涉及对气道平滑肌的直接作用。因此,我们通过测量豚鼠气管平滑肌的等长张力,比较了地西泮、氟硝西泮和咪达唑仑对气道张力的影响。地西泮、氟硝西泮和咪达唑仑的累积浓度导致气管平滑肌静息张力呈浓度依赖性松弛,三种化合物的pD2值(-log EC50,效力指标)或松弛的内在活性(最大反应的百分比)无显著差异。用10⁻⁶mol/L普萘洛尔、10⁻⁷和10⁻⁶mol/L氟马西尼或10⁻⁶mol/L PK11195预处理对地西泮或咪达唑仑诱导的松弛无影响。3×10⁻⁶mol/L地西泮预处理使乙酰胆碱、组胺和5-羟色胺(5-HT)的浓度-反应曲线右移约2倍。3×10⁻⁶mol/L氟硝西泮预处理也使组胺和5-HT的曲线类似地右移,而咪达唑仑预处理不抑制任何激动剂诱导的收缩。这些结果表明,苯二氮䓬类药物松弛气道平滑肌不是通过神经途径或中枢及外周苯二氮䓬受体,而是通过对气道平滑肌的直接作用。