Derwall M, Coburn M, Rex S, Hein M, Rossaint R, Fries M
Department of Anesthesiology, University Hospital Aachen, RWTH Aachen, Germany.
Minerva Anestesiol. 2009 Jan-Feb;75(1-2):37-45. Epub 2008 May 15.
The noble gas xenon exerts favorable anesthetic properties along with remarkable hemodynamic stability in healthy patients undergoing elective surgery. Recent investigations documented that it does not prolong the duration of widely used neuromuscular blocking agents, including mivacurium and rocuronium. Some studies also suggest reduced neurocognitive compromise in the very early phase after general anesthesia. These properties differ from those observed for conventional inhalational anesthetics like isoflurane, desflurane and sevoflurane. However, a wider use of xenon in daily clinical routine has been limited owing to its higher price and technical restraints regarding economic delivery. Although there are controversial opinions, xenon seems to exert its main anesthetic features via the glutamate receptor. Recently, a novel binding cavity on the NMDA-subtype glutamate receptor has been elucidated that is occupied by xenon as well as isoflurane. Studies utilizing advanced imaging technologies have furthermore revealed that xenon markedly suppresses cerebral blood flow and glucose metabolism in distinct regions of the human brain. These investigations promise to further the understanding of the basic mechanisms underlying the induction and maintenance of anesthesia in general. Results from in vitro studies and various animal models have consistently demonstrated organoprotective properties of xenon, mainly in settings of ischemia and reperfusion injury. Interestingly, these effects have frequently been observed at subanesthetic concentrations and seem to be synergistic when used in combination with therapeutic hypothermia. Future studies will have to prove whether the high costs of xenon administration might be outweighed by its ability to substantially reduce the sequelae of myocardial and cerebral ischemia.
在接受择期手术的健康患者中,稀有气体氙具有良好的麻醉特性以及显著的血流动力学稳定性。最近的研究表明,它不会延长包括米库氯铵和罗库溴铵在内的广泛使用的神经肌肉阻滞剂的作用时间。一些研究还表明,在全身麻醉后的极早期,它能减少神经认知功能损害。这些特性与异氟烷、地氟烷和七氟烷等传统吸入麻醉剂不同。然而,由于其价格较高以及在经济输送方面的技术限制,氙在日常临床实践中的广泛应用受到了限制。尽管存在争议,但氙似乎主要通过谷氨酸受体发挥其麻醉作用。最近,已阐明了NMDA亚型谷氨酸受体上的一个新结合腔,氙和异氟烷均可占据该腔。利用先进成像技术的研究还进一步表明,氙能显著抑制人脑不同区域的脑血流量和葡萄糖代谢。这些研究有望进一步加深对全身麻醉诱导和维持的基本机制的理解。体外研究和各种动物模型的结果一致表明,氙具有器官保护特性,主要在缺血和再灌注损伤的情况下。有趣的是,这些作用经常在亚麻醉浓度下观察到,并且与治疗性低温联合使用时似乎具有协同作用。未来的研究将不得不证明,氙给药的高成本是否可能被其大幅减少心肌和脑缺血后遗症的能力所抵消。