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本文引用的文献

1
Medial septal cholinergic neurons modulate isoflurane anesthesia.中隔胆碱能神经元调节异氟醚麻醉。
Anesthesiology. 2014 Feb;120(2):392-402. doi: 10.1097/ALN.0b013e3182a7cab6.
2
Adenosine receptors as drug targets--what are the challenges?腺苷受体作为药物靶点——存在哪些挑战?
Nat Rev Drug Discov. 2013 Apr;12(4):265-86. doi: 10.1038/nrd3955.
3
Activation of D1 dopamine receptors induces emergence from isoflurane general anesthesia.D1 多巴胺受体的激活可诱导异氟醚全身麻醉苏醒。
Anesthesiology. 2013 Jan;118(1):30-9. doi: 10.1097/ALN.0b013e318278c896.
4
Presynaptic inhibition of the release of multiple major central nervous system neurotransmitter types by the inhaled anaesthetic isoflurane.吸入麻醉剂异氟烷对中枢神经系统多种主要神经递质释放的突触前抑制作用。
Br J Anaesth. 2013 Apr;110(4):592-9. doi: 10.1093/bja/aes448. Epub 2012 Dec 4.
5
Distinct initial SNARE configurations underlying the diversity of exocytosis.不同的初始 SNARE 构型是胞吐多样性的基础。
Physiol Rev. 2012 Oct;92(4):1915-64. doi: 10.1152/physrev.00007.2012.
6
Active emergence from propofol general anesthesia is induced by methylphenidate.哌醋甲酯可诱导丙泊酚全身麻醉后的主动苏醒。
Anesthesiology. 2012 May;116(5):998-1005. doi: 10.1097/ALN.0b013e3182518bfc.
7
A gain-of-function mutation in adenylate cyclase confers isoflurane resistance in Caenorhabditis elegans.腺嘌呤环化酶的功能获得性突变赋予秀丽隐杆线虫对异氟烷的耐药性。
Anesthesiology. 2011 Dec;115(6):1162-71. doi: 10.1097/ALN.0b013e318239355d.
8
Cognitive and behavioral outcomes after early exposure to anesthesia and surgery.早期接触麻醉和手术对认知和行为的影响。
Pediatrics. 2011 Nov;128(5):e1053-61. doi: 10.1542/peds.2011-0351. Epub 2011 Oct 3.
9
Methylphenidate actively induces emergence from general anesthesia.哌醋甲酯能主动诱导全麻苏醒。
Anesthesiology. 2011 Oct;115(4):791-803. doi: 10.1097/ALN.0b013e31822e92e5.
10
Arousal effect of caffeine depends on adenosine A2A receptors in the shell of the nucleus accumbens.咖啡因的觉醒效应取决于伏隔核壳部的腺苷 A2A 受体。
J Neurosci. 2011 Jul 6;31(27):10067-75. doi: 10.1523/JNEUROSCI.6730-10.2011.

咖啡因可加速全身麻醉后的恢复。

Caffeine accelerates recovery from general anesthesia.

机构信息

Department of Neurobiology, Pharmacology and Physiology, University of Chicago, Chicago, Illinois;

出版信息

J Neurophysiol. 2014 Mar;111(6):1331-40. doi: 10.1152/jn.00792.2013. Epub 2013 Dec 26.

DOI:10.1152/jn.00792.2013
PMID:24375022
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3949308/
Abstract

General anesthetics inhibit neurotransmitter release from both neurons and secretory cells. If inhibition of neurotransmitter release is part of an anesthetic mechanism of action, then drugs that facilitate neurotransmitter release may aid in reversing general anesthesia. Drugs that elevate intracellular cAMP levels are known to facilitate neurotransmitter release. Three cAMP elevating drugs (forskolin, theophylline, and caffeine) were tested; all three drugs reversed the inhibition of neurotransmitter release produced by isoflurane in PC12 cells in vitro. The drugs were tested in isoflurane-anesthetized rats. Animals were injected with either saline or saline containing drug. All three drugs dramatically accelerated recovery from isoflurane anesthesia, but caffeine was most effective. None of the drugs, at the concentrations tested, had significant effects on breathing rates, O2 saturation, heart rate, or blood pressure in anesthetized animals. Caffeine alone was tested on propofol-anesthetized rats where it dramatically accelerated recovery from anesthesia. The ability of caffeine to accelerate recovery from anesthesia for different chemical classes of anesthetics, isoflurane and propofol, opens the possibility that it will do so for all commonly used general anesthetics, although additional studies will be required to determine whether this is in fact the case. Because anesthesia in rodents is thought to be similar to that in humans, these results suggest that caffeine might allow for rapid and uniform emergence from general anesthesia in human patients.

摘要

全身麻醉会抑制神经元和分泌细胞的神经递质释放。如果神经递质释放抑制是全身麻醉作用机制的一部分,那么促进神经递质释放的药物可能有助于逆转全身麻醉。已知升高细胞内 cAMP 水平的药物可促进神经递质释放。测试了三种升高 cAMP 的药物(forskolin、茶碱和咖啡因);这三种药物均能逆转异氟烷在体外对 PC12 细胞神经递质释放的抑制作用。在异氟烷麻醉的大鼠中测试了这些药物。动物注射盐水或含药盐水。这三种药物都能显著加速异氟烷麻醉的恢复,但咖啡因效果最显著。在麻醉动物中,在测试浓度下,这些药物对呼吸频率、O2 饱和度、心率或血压均无显著影响。单独测试了咖啡因对异丙酚麻醉大鼠的作用,结果表明它能显著加速麻醉恢复。咖啡因能够加速不同化学类别的全身麻醉药(异氟烷和异丙酚)的麻醉恢复,这为它可能对所有常用的全身麻醉药都有效开辟了可能性,尽管还需要进一步的研究来确定这是否属实。由于啮齿动物的麻醉被认为与人类相似,这些结果表明,咖啡因可能会使人类患者能够快速、均匀地从全身麻醉中苏醒。