Schlünzen L, Cold G E, Rasmussen M, Vafaee M S
Department of Neuroanaesthesiology, Aarhus University Hospital, Aarhus, Denmark.
Acta Anaesthesiol Scand. 2006 Mar;50(3):306-12. doi: 10.1111/j.1399-6576.2006.00954.x.
In this study, we tested the hypothesis that escalating drug concentrations of isoflurane are associated with a significant decline in cerebral blood flow (CBF) in regions sub-serving conscious brain activity, including specifically the thalamus.
Nine human volunteers received three escalating drug concentrations: 0.2, 0.4 and 1.0 MAC end-tidal inhalation. During waking, baseline and the three levels of sedation, aO PET scan was performed.
Isoflurane decreased the bispectral index (BIS) values dose-dependently. Cardiovascular and respiratory parameters were maintained constant over time. No significant change in global CBF was observed. Throughout all three MAC levels of sedation, isoflurane caused an increased regional cerebral blood flow (rCBF) in the anterior cingulate and decreased rCBF in the cerebellum. Initially, isoflurane (0 vs. 0.2 MAC) significantly increased relative rCBF in the medial frontal gyrus and in the nucleus accumbens. At the next level (0.2 vs. 0.4 MAC), relative rCBF was significantly increased in the caudate nucleus and decreased in the lingual gyrus and cuneus. At the last level (0.4 vs. 1 MAC), relative rCBF was significantly increased in the insula and decreased in the thalamus, the cuneus and lingual gyrus. Compared with flow distribution in awake volunteers, 1 MAC of isoflurane significantly raised relative activity in the anterior cingulate and insula regions. In contrast, a significant relative flow reduction was identified in the thalamus, the cerebellum and lingual gyrus.
Isoflurane, like sevoflurane, induced characteristic flow redistribution at doses of 0.2-1.0 MAC. At 1 MAC of isoflurane, rCBF decreased in the thalamus. Specific areas affected by both isoflurane and sevoflurane included the anterior cingulate, insula regions, cerebellum, lingual gyrus and thalamus.
在本研究中,我们检验了以下假设:异氟烷药物浓度的逐步升高与维持意识脑活动的区域(特别是丘脑)的脑血流量(CBF)显著下降相关。
九名人类志愿者接受了三种逐步升高的药物浓度:呼气末吸入0.2、0.4和1.0 MAC。在清醒、基线状态以及三种镇静水平期间,进行了动脉自旋标记(aO)PET扫描。
异氟烷使脑电双频指数(BIS)值呈剂量依赖性降低。心血管和呼吸参数随时间保持恒定。未观察到全脑CBF有显著变化。在所有三种MAC水平的镇静过程中,异氟烷导致前扣带回区域的局部脑血流量(rCBF)增加,小脑的rCBF减少。最初,异氟烷(0与0.2 MAC相比)使内侧前额叶皮质和伏隔核的相对rCBF显著增加。在下一个水平(0.2与0.4 MAC相比),尾状核的相对rCBF显著增加,舌回和楔叶的相对rCBF减少。在最后一个水平(0.4与1 MAC相比),岛叶的相对rCBF显著增加,丘脑、楔叶和舌回的相对rCBF减少。与清醒志愿者的血流分布相比,1 MAC的异氟烷显著提高了前扣带回和岛叶区域的相对活性。相反,在丘脑、小脑和舌回中发现了显著的相对血流减少。
与七氟烷一样,异氟烷在0.2 - 1.0 MAC剂量下会引起特征性的血流重新分布。在1 MAC的异氟烷时,丘脑的rCBF下降。受异氟烷和七氟烷影响的特定区域包括前扣带回、岛叶区域、小脑、舌回和丘脑。