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钙通道阻滞剂对恶性高热危象无效。

Calcium channel blockers are inadequate for malignant hyperthermia crisis.

机构信息

Division of Anesthesia, Hiroshima Red Cross Hospital and Atomic-Bomb Survivors Hospital, 1-9-6 Senda-machi, Naka-ku, Hiroshima, 730-8619, Japan.

出版信息

J Anesth. 2012 Aug;26(4):579-84. doi: 10.1007/s00540-012-1347-0. Epub 2012 Feb 16.

Abstract

PURPOSE

Malignant hyperthermia (MH) results from disordered calcium (Ca(2+)) homeostasis in skeletal muscle during general anesthesia. Although Ca(2+) channel blockers may be given to treat the tachycardia and circulatory instability, coadministration of Ca(2+) channel blockers and dantrolene is contraindicated during MH crisis. We evaluated the effect of Ca(2+) channel blockers on Ca(2+) homeostasis and their interactions with dantrolene in human skeletal muscle.

METHODS

Human skeletal muscle samples were obtained by biopsy and divided into two groups according to the results of the Ca(2+)-induced Ca(2+) release rate test. Differentiated myotubes were labeled with Fura-2, and changes in the 340/380-nm ratio were used to calculate changes in Ca(2+) concentration following nifedipine treatment in the absence or presence of dantrolene.

RESULTS

Nifedipine induced a transient increase in the intracellular Ca(2+) concentration (Ca(2+)) in a dose-dependent manner. The half-maximal concentration (EC(50)) for nifedipine was 0.718 ± 0.329 μM in the accelerated group and 1.389 ± 0.482 μM in the nonaccelerated group (P = 0.009). The addition of 50 μM dantrolene attenuated by 15.4% the increase in Ca(2+) caused by the 0.5 μM nifedipine.

CONCLUSION

Ca(2+) channel blockers led to increased Ca(2+) in human skeletal muscle cells. The increase is thus scarcely affected by dantrolene treatment. Data provide a greater physiologic basis for avoiding the use of Ca(2+) channel blockers during MH crisis.

摘要

目的

恶性高热(MH)是全身麻醉时骨骼肌中钙(Ca(2+))稳态紊乱引起的。尽管可以给予 Ca(2+)通道阻滞剂来治疗心动过速和循环不稳定,但在 MH 危机期间,Ca(2+)通道阻滞剂和丹曲林钠不能同时使用。我们评估了 Ca(2+)通道阻滞剂对 Ca(2+)稳态的影响及其与丹曲林钠的相互作用在人体骨骼肌中。

方法

通过活检获得人体骨骼肌样本,并根据 Ca(2+)诱导的 Ca(2+)释放率试验的结果将其分为两组。分化的肌管用 Fura-2 标记,并用 340/380nm 比值的变化来计算硝苯地平治疗时有无丹曲林钠存在下 Ca(2+)浓度的变化。

结果

硝苯地平以剂量依赖的方式诱导细胞内 Ca(2+)浓度([Ca(2+)](i))的短暂增加。在加速组中,硝苯地平的半最大浓度(EC(50))为 0.718±0.329μM,在非加速组中为 1.389±0.482μM(P=0.009)。添加 50μM 丹曲林钠可使 0.5μM 硝苯地平引起的 [Ca(2+)](i)增加减少 15.4%。

结论

Ca(2+)通道阻滞剂导致人体骨骼肌细胞中 [Ca(2+)](i)增加。因此,丹曲林钠的处理对其影响很小。这些数据为避免 MH 危机期间使用 Ca(2+)通道阻滞剂提供了更大的生理基础。

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