钙通道激动剂(BAY K8644)对新生儿兔乳头肌挥发性麻醉抑制的影响。

V C Baum, T S Klitzner
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引用次数: 0

摘要

心肌依赖于细胞外液钙的进入来支持收缩,新生儿心脏对钙经肌层进入的减少特别敏感。因此,本研究评估了钙通道激动剂BAY K8644预防或逆转氟烷或异氟烷对新生兔右心室乳头肌心肌抑制作用的能力。研究了BAY K8644逆转力(F)和dF/dt(氟烷和异氟烷)还原或阻止还原(氟烷)的能力。氟化烷使F降低到基线值的24±2% (p = 0.001)。加入BAY K8644后,F值仅为基线值的54±3% (p = 0.001, p = 0.002)。异氟醚将F降低到基线的20 +/- 2% (p = 0.001),添加BAY K8644后返回到基线的45 +/- 4% (p = 0.0001与基线相比,p = 0.0025与单独使用异氟醚相比)。在加入氟烷之前,将BAY K8644放入培养液中,氟烷将F降低至基线的38 +/- 4% (p = 0.001)。dF/dt反映了所有研究中F的变化。这些数据表明,钙通道激动剂在调节新生儿兔心室乳头肌挥发性麻醉诱导的抑郁中仅部分有效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of calcium channel agonist (BAY K8644) on volatile anesthetic-mediated depression in neonatal rabbit papillary muscle.

Heart muscle is dependent on the entry of calcium from the extracellular fluid to support contraction, and neonatal hearts are particularly sensitive to reductions in transsarcolemmal entry of calcium. Accordingly, this study evaluated the ability of the calcium channel agonist BAY K8644 to prevent or reverse the myocardial depressant effects of halothane or isoflurane in right ventricular papillary muscles from neonatal rabbits. The ability of BAY K8644 to reverse reductions in force (F) and dF/dt (halothane and isoflurane) or prevent reduction (halothane) was studied. Halothane decreased F to 24 +/- 2% of baseline values (p = 0.001). The addition of BAY K8644 reversed F to only 54 +/- 3% of baseline (p = 0.001 vs. baseline and p = 0.002 vs. halothane alone). Isoflurane decreased F to 20 +/- 2% of baseline (p = 0.001) with a return to 45 +/- 4% of baseline with the addition of BAY K8644 (p = 0.0001 vs. baseline and p = 0.0025 vs. isoflurane alone). With BAY K8644 in the bath prior to the addition of halothane, halothane decreased F to 38 +/- 4% of baseline (p = 0.001). dF/dt mirrored changes in F in all studies. These data show that a calcium channel agonist is only partially effective in modulating volatile anesthetic-induced depression in neonatal rabbit ventricular papillary muscle.

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