Wang Lan, Traystman Richard J, Murphy Stephanie J
Oregon Health and Science University, Department of Anesthesiology and Peri-Operative Medicine, 3181 SW Sam Jackson Park Road, Portland, OR 97239-3098, USA.
Curr Opin Pharmacol. 2008 Feb;8(1):104-10. doi: 10.1016/j.coph.2007.09.005. Epub 2007 Oct 24.
While many pharmacological agents have been shown to protect the brain from cerebral ischemia in animal models, none have translated successfully to human patients. One potential clinical neuroprotective strategy in humans may involve increasing the brain's tolerance to ischemia by preischemic conditioning (preconditioning). There are many methods to induce tolerance via preconditioning such as ischemia itself, pharmacological, hypoxia, endotoxin, and others. Inhalational anesthetic agents have also been shown to result in brain preconditioning. Mechanisms responsible for brain preconditioning are many, complex, and unclear and may involve Akt activation, ATP-sensitive potassium channels, and nitric oxide, amongst many others. Anesthetics, however, may play an important and unique role as preconditioning agents, particularly during the perioperative period.
虽然在动物模型中已证明许多药物制剂可保护大脑免受脑缺血损伤,但尚无一种能成功应用于人类患者。人类一种潜在的临床神经保护策略可能是通过缺血预处理(预适应)来提高大脑对缺血的耐受性。有许多方法可通过预适应诱导耐受性,如缺血本身、药物、缺氧、内毒素等。吸入性麻醉剂也已被证明可导致脑预适应。负责脑预适应的机制众多、复杂且尚不清楚,可能涉及Akt激活、ATP敏感性钾通道、一氧化氮等多种因素。然而,麻醉剂作为预适应剂可能发挥重要且独特的作用,尤其是在围手术期。