Seidemann Thomas, Spies Claudia, Morgenstern Rudolf, Wernecke Klaus-Dieter, Netzhammer Nicolai
Department of Anesthesiology and Intensive Care Medicine, Campus Charité Mitte and Campus Virchow-Klinikum, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Institute of Pharmacology, Campus Charité Mitte, Charité - Universitätsmedizin Berlin, Berlin, Germany.
PLoS One. 2017 Jan 3;12(1):e0169017. doi: 10.1371/journal.pone.0169017. eCollection 2017.
Alcohol withdrawal syndrome is a potentially life-threatening condition, which can occur when patients with alcohol use disorders undergo general anesthesia. Excitatory amino acids, such as glutamate, act as neurotransmitters and are known to play a key role in alcohol withdrawal syndrome. To understand this process better, we investigated the influence of isoflurane, sevoflurane, and desflurane anesthesia on the profile of excitatory and inhibitory amino acids in the nucleus accumbens (NAcc) of alcohol-withdrawn rats (AWR).
Eighty Wistar rats were randomized into two groups of 40, pair-fed with alcoholic or non-alcoholic nutrition. Nutrition was withdrawn and microdialysis was performed to measure the activity of amino acids in the NAcc. The onset time of the withdrawal syndrome was first determined in an experiment with 20 rats. Sixty rats then received isoflurane, sevoflurane, or desflurane anesthesia for three hours during the withdrawal period, followed by one hour of elimination. Amino acid concentrations were measured using chromatography and results were compared to baseline levels measured prior to induction of anesthesia.
Glutamate release increased in the alcohol group at five hours after the last alcohol intake (p = 0.002). After 140 min, desflurane anesthesia led to a lower release of glutamate (p < 0.001) and aspartate (p = 0.0007) in AWR compared to controls. GABA release under and after desflurane anesthesia was also significantly lower in AWR than controls (p = 0.023). Over the course of isoflurane anesthesia, arginine release decreased in AWR compared to controls (p < 0.001), and aspartate release increased after induction relative to controls (p20min = 0.015 and p40min = 0.006). However, amino acid levels did not differ between the groups as a result of sevoflurane anesthesia.
Each of three volatile anesthetics we studied showed different effects on excitatory and inhibitory amino acid concentrations. Under desflurane anesthesia, both glutamate and aspartate showed a tendency to be lower in AWR than controls over the whole timecourse. The inhibitory amino acid arginine increased in AWR compared to controls, whereas GABA levels decreased. However, there were no significant differences in amino acid concentrations under or after sevoflurane anesthesia. Under isoflurane, aspartate release increased in AWR following induction, and from 40 min to 140 min arginine release in controls was elevated. The precise mechanisms through which each of the volatile anesthetics affected amino acid concentrations are still unclear and further experimental research is required to draw reliable conclusions.
酒精戒断综合征是一种潜在的危及生命的状况,可发生于酒精使用障碍患者接受全身麻醉时。兴奋性氨基酸,如谷氨酸,作为神经递质,已知在酒精戒断综合征中起关键作用。为了更好地理解这一过程,我们研究了异氟烷、七氟烷和地氟烷麻醉对酒精戒断大鼠(AWR)伏隔核(NAcc)中兴奋性和抑制性氨基酸谱的影响。
80只Wistar大鼠随机分为两组,每组40只,分别给予酒精或非酒精营养配对喂养。停止营养供应并进行微透析以测量NAcc中氨基酸的活性。首先在20只大鼠的实验中确定戒断综合征的发作时间。然后60只大鼠在戒断期接受异氟烷、七氟烷或地氟烷麻醉3小时,随后进行1小时的恢复期。使用色谱法测量氨基酸浓度,并将结果与麻醉诱导前测量的基线水平进行比较。
酒精组在最后一次摄入酒精后5小时谷氨酸释放增加(p = 0.002)。140分钟后,与对照组相比,地氟烷麻醉导致AWR中谷氨酸(p < 0.001)和天冬氨酸(p = 0.0007)释放降低。地氟烷麻醉期间及之后,AWR中GABA释放也显著低于对照组(p = 0.023)。在异氟烷麻醉过程中,与对照组相比,AWR中精氨酸释放减少(p < 0.001),诱导后相对于对照组天冬氨酸释放增加(p20分钟 = 0.015和p40分钟 = 0.006)。然而,七氟烷麻醉后两组间氨基酸水平无差异。
我们研究的三种挥发性麻醉剂对兴奋性和抑制性氨基酸浓度均显示出不同的影响。在地氟烷麻醉下,整个时间段内AWR中谷氨酸和天冬氨酸均有低于对照组的趋势。与对照组相比,AWR中抑制性氨基酸精氨酸增加,而GABA水平降低。然而,七氟烷麻醉期间及之后氨基酸浓度无显著差异。在异氟烷麻醉下,诱导后AWR中天冬氨酸释放增加,且在40分钟至140分钟期间对照组中精氨酸释放升高。每种挥发性麻醉剂影响氨基酸浓度的确切机制仍不清楚,需要进一步的实验研究以得出可靠结论。