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挥发性麻醉药对气道平滑肌Ca2+致敏的药物特异性作用。

Drug-specific effects of volatile anesthetics on Ca2+ sensitization in airway smooth muscle.

作者信息

Kai T, Bremerich D H, Jones K A, Warner D O

机构信息

Department of Anesthesiology, Mayo Clinic and Mayo Foundation, Rochester, Minnesota 55905, USA.

出版信息

Anesth Analg. 1998 Aug;87(2):425-9. doi: 10.1097/00000539-199808000-00036.

Abstract

UNLABELLED

Halothane directly relaxes airway smooth muscle, partly by decreasing the Ca2+ sensitivity during membrane receptor stimulation. The effects of other volatile anesthetics on Ca2+ sensitivity are unclear. In the current study, we compared the ability of halothane, sevoflurane, and isoflurane to inhibit increases in Ca2+ sensitivity during muscarinic receptor stimulation. Beta-escin-permeabilized canine tracheal smooth muscle strips were used. Anesthetics were applied during contractions induced by 3 microM acetylcholine and 10 microM guanosine 5'-triphosphate at a constant cytosolic Ca2+ concentration of 0.3 microM. Effects were evaluated as a percent relaxation from initial force corrected for time. Halothane significantly decreased force at both low (0.76 minimum alveolar anesthetic concentration [MAC]) and high (1.8 MAC) concentrations in a concentration-dependent manner. Sevoflurane also decreased force, significantly so at a high concentration (1.7 MAC). Isoflurane did not significantly affect force even at a high concentration (1.7 MAC). Halothane's relaxing effect was significantly greater than that of the other two anesthetics at each corresponding MAC concentration. Among these three volatile anesthetics compared at equipotent anesthetic concentrations, halothane was the most potent in reducing Ca2+ sensitivity during muscarinic receptor stimulation in canine tracheal smooth muscle. This may contribute to halothane's greater relaxing effect compared with isoflurane at the same MAC concentrations in intact airway smooth muscle.

IMPLICATIONS

In this study, we showed that three volatile anesthetics (halothane, sevoflurane, and isoflurane) compared at equipotent anesthetic concentrations differed in their ability to inhibit Ca2+ sensitivity during muscarinic receptor stimulation in airway smooth muscle. The potency order was halothane > sevoflurane > or = isoflurane.

摘要

未标记

氟烷可直接舒张气道平滑肌,部分原因是在膜受体刺激过程中降低了钙离子敏感性。其他挥发性麻醉药对钙离子敏感性的影响尚不清楚。在本研究中,我们比较了氟烷、七氟烷和异氟烷在毒蕈碱受体刺激过程中抑制钙离子敏感性增加的能力。使用了经β-七叶皂苷渗透的犬气管平滑肌条。在3微摩尔乙酰胆碱和10微摩尔鸟苷5'-三磷酸诱导收缩期间,在细胞溶质钙离子浓度恒定为0.3微摩尔的情况下应用麻醉药。将效应评估为相对于初始力经时间校正后的舒张百分比。氟烷在低浓度(0.76最低肺泡麻醉浓度[MAC])和高浓度(1.8 MAC)时均以浓度依赖性方式显著降低张力。七氟烷也降低了张力,在高浓度(1.7 MAC)时显著降低。异氟烷即使在高浓度(1.7 MAC)时也未显著影响张力。在每个相应的MAC浓度下,氟烷的舒张作用明显大于其他两种麻醉药。在等效能麻醉浓度下比较的这三种挥发性麻醉药中,氟烷在犬气管平滑肌毒蕈碱受体刺激过程中降低钙离子敏感性的作用最强。这可能有助于解释在相同MAC浓度下,与异氟烷相比,氟烷在完整气道平滑肌中具有更大的舒张作用。

启示

在本研究中,我们表明在等效能麻醉浓度下比较的三种挥发性麻醉药(氟烷、七氟烷和异氟烷)在气道平滑肌毒蕈碱受体刺激过程中抑制钙离子敏感性的能力不同。效能顺序为氟烷>七氟烷>或=异氟烷。

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