Piriou V, Chiari P, Lhuillier F, Bastien O, Loufoua J, Raisky O, David J S, Ovize M, Lehot J J
Service d'Anesthésie Réanimation, Hôpital cardio-vasculaire Louis Pradel, Avenue Doyen Lépine, F-69500 Lyon Bron, France.
Br J Anaesth. 2002 Sep;89(3):486-91.
Recent investigations showed that isoflurane can induce pharmacological preconditioning. The present study aimed to compare the potency of four different halogenated anaesthetics to induce preconditioning.
Anaesthetized open-chest rabbits underwent 30 min of coronary artery occlusion followed by 3 h of reperfusion. Before this, rabbits were randomized into one of five groups and underwent a treatment period consisting of either no intervention for 45 min (control; n = 10), or 30 min of 1 MAC halogenated anaesthetic inhalation followed by 15 min of washout. End-tidal concentrations of halogenated agents were 3.7% for sevoflurane (n = 11), 1.4% for halothane (n = 9), 2.0% for isoflurane (n = 11), and 8.9% for desflurane (n = 11). Area at risk and infarct size were assessed by blue dye injection and tetrazolium chloride staining.
Mean (SD) infarct size was 54 (18)% of the risk area in untreated controls and 40 (18)% in the sevoflurane group (P > 0.05, ns). In contrast, mean infarct size was significantly smaller in the halothane, isoflurane, and desflurane groups: 26 (18)%, 32 (18)% and 16 (17)%, respectively (P < 0.05 vs control).
Halothane, isoflurane and desflurane induced pharmacological preconditioning, whereas sevoflurane had no significant effect. In this preparation, desflurane was the most effective agent at preconditioning the myocardium against ischaemia.
近期研究表明异氟烷可诱导药理学预处理。本研究旨在比较四种不同卤代麻醉剂诱导预处理的效能。
麻醉开胸兔冠状动脉闭塞30分钟,随后再灌注3小时。在此之前,将兔随机分为五组之一,接受一个治疗期,包括45分钟无干预(对照组;n = 10),或吸入1 MAC卤代麻醉剂30分钟,随后冲洗15分钟。七氟烷(n = 11)的呼气末浓度为3.7%,氟烷(n = 9)为1.4%,异氟烷(n = 11)为2.0%,地氟烷(n = 11)为8.9%。通过注射蓝色染料和氯化三苯基四氮唑染色评估危险面积和梗死面积。
未治疗对照组梗死面积平均(标准差)为危险区域的54(18)%,七氟烷组为40(18)%(P > 0.05,无显著差异)。相比之下,氟烷、异氟烷和地氟烷组的平均梗死面积显著较小:分别为26(18)%、32(18)%和16(17)%(与对照组相比P < 0.05)。
氟烷、异氟烷和地氟烷可诱导药理学预处理,而七氟烷无显著作用。在此制剂中,地氟烷是预处理心肌抗缺血最有效的药物。