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本文引用的文献

1
Requested retraction of six studies on the PK/PD and tolerability of fospropofol.
Anesth Analg. 2010 Apr 1;110(4):1240. doi: 10.1213/ANE.0b013e3181d82560.
2
Cognitive function after major noncardiac surgery, apolipoprotein E4 genotype, and biomarkers of brain injury.重大非心脏手术后的认知功能、载脂蛋白 E4 基因型和脑损伤的生物标志物。
Anesthesiology. 2010 Apr;112(4):852-9. doi: 10.1097/ALN.0b013e3181d31fd7.
3
Carboetomidate: a pyrrole analog of etomidate designed not to suppress adrenocortical function.卡泊芬净:一种吡咯烷酮类似物,设计用于不抑制肾上腺皮质功能。
Anesthesiology. 2010 Mar;112(3):637-44. doi: 10.1097/ALN.0b013e3181cf40ed.
4
Argon: neuroprotection in in vitro models of cerebral ischemia and traumatic brain injury.氩气:在体外脑缺血和创伤性脑损伤模型中的神经保护作用。
Crit Care. 2009;13(6):R206. doi: 10.1186/cc8214. Epub 2009 Dec 17.
5
Neurotoxicity of general anesthetics: cause for concern?全身麻醉药的神经毒性:值得关注吗?
Anesthesiology. 2009 Dec;111(6):1365-71. doi: 10.1097/ALN.0b013e3181bf1d61.
6
Reduced immobilizing properties of isoflurane and nitrous oxide in mutant mice lacking the N-methyl-D-aspartate receptor GluR(epsilon)1 subunit are caused by the secondary effects of gene knockout.突变型小鼠缺乏 N-甲基-D-天冬氨酸受体 GluR(epsilon)1 亚单位,导致异氟烷和氧化亚氮的固定作用降低,这是基因敲除的继发效应所致。
Anesth Analg. 2010 Feb 1;110(2):461-5. doi: 10.1213/ANE.0b013e3181c76e73. Epub 2009 Nov 21.
7
A high-throughput approach for identification of novel general anesthetics.高通量筛选新型全身麻醉剂的方法。
PLoS One. 2009 Sep 24;4(9):e7150. doi: 10.1371/journal.pone.0007150.
8
Methoxycarbonyl-etomidate: a novel rapidly metabolized and ultra-short-acting etomidate analogue that does not produce prolonged adrenocortical suppression.甲氧基羰基依托咪酯:一种新型的快速代谢且超短效的依托咪酯类似物,不会产生长期的肾上腺皮质抑制。
Anesthesiology. 2009 Aug;111(2):240-9. doi: 10.1097/ALN.0b013e3181ae63d1.
9
A unitary anesthetic binding site at high resolution.高分辨率下的单一麻醉剂结合位点。
J Biol Chem. 2009 Sep 4;284(36):24176-84. doi: 10.1074/jbc.M109.017814. Epub 2009 Jul 15.
10
General anesthetics and the developing brain.全身麻醉与发育中的大脑。
Curr Opin Anaesthesiol. 2009 Jun;22(3):368-73. doi: 10.1097/aco.0b013e3283294c9e.

改善全身麻醉剂的分子方法。

Molecular approaches to improving general anesthetics.

作者信息

Forman Stuart A

机构信息

Department of Anesthesia, Critical Care & Pain Medicine, Massachusetts General Hospital, Jackson 4, MGH, 55 Fruit Street, Boston, MA 02114, USA.

出版信息

Anesthesiol Clin. 2010 Dec;28(4):761-71. doi: 10.1016/j.anclin.2010.08.004.

DOI:10.1016/j.anclin.2010.08.004
PMID:21074751
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2990980/
Abstract

Over the last several decades, the average age of patients has steadily increased, whereas the use of general anesthesia and deep sedation has grown largely outside the operating room environment. Currently available general anesthetics and delivery models represent limitations in addressing these trends. At the same time, research has tremendously expanded the knowledge of how general anesthetics produce their beneficial effects and also revealed evidence of previously unappreciated general anesthetic toxicities. The goal of this review is to highlight these important developments and describe translational research on new general anesthetics with the potential to improve and reshape clinical care.

摘要

在过去几十年中,患者的平均年龄稳步上升,而全身麻醉和深度镇静的使用在很大程度上已扩展至手术室环境之外。目前可用的全身麻醉药和给药模式在应对这些趋势方面存在局限性。与此同时,研究极大地扩展了我们对全身麻醉药如何产生有益作用的认识,也揭示了此前未被认识到的全身麻醉药毒性的证据。本综述的目的是突出这些重要进展,并描述关于新型全身麻醉药的转化研究,这些研究有可能改善和重塑临床护理。