University College London Institute of Ophthalmology, London EC1V 9EL, United Kingdom.
University College London Institute of Ophthalmology, London EC1V 9EL, United Kingdom
J Lipid Res. 2017 Oct;58(10):1962-1976. doi: 10.1194/jlr.M073932. Epub 2017 Aug 17.
There is great individual variation in response to general anesthetics (GAs) leading to difficulties in optimal dosing and sometimes even accidental awareness during general anesthesia (AAGA). AAGA is a rare, but potentially devastating, complication affecting between 0.1% and 2% of patients undergoing surgery. The development of novel personalized screening techniques to accurately predict a patient's response to GAs and the risk of AAGA remains an unmet clinical need. In the present study, we demonstrate the principle of using a fluorescent reporter of the membrane dipole potential, di-8-ANEPPs, as a novel method to monitor anesthetic activity using a well-described inducer/noninducer pair. The membrane dipole potential has previously been suggested to contribute a novel mechanism of anesthetic action. We show that the fluorescence ratio of di-8-ANEPPs changed in response to physiological concentrations of the anesthetic, 1-chloro-1,2,2-trifluorocyclobutane (F), but not the structurally similar noninducer, 1,2-dichlorohexafluorocyclobutane (F), to artificial membranes and in vitro retinal cell systems. Modulation of the membrane dipole provides an explanation to overcome the limitations associated with the alternative membrane-mediated mechanisms of GA action. Furthermore, by combining this technique with noninvasive retinal imaging technologies, we propose that this technique could provide a novel and noninvasive technique to monitor GA susceptibility and identify patients at risk of AAGA.
个体对全身麻醉药(GAs)的反应存在很大差异,这导致在最佳剂量方面存在困难,有时甚至在全身麻醉期间会出现意外意识(AAGA)。AAGA 是一种罕见但潜在破坏性的并发症,影响接受手术的患者的 0.1%至 2%。开发新型个性化筛选技术来准确预测患者对 GAs 的反应和 AAGA 的风险仍然是未满足的临床需求。在本研究中,我们展示了使用膜偶极势的荧光报告子 di-8-ANEPPs 的原理,作为一种使用描述良好的诱导剂/非诱导剂对监测麻醉活性的新方法。膜偶极势先前被认为是麻醉作用的一种新机制。我们表明,di-8-ANEPPs 的荧光比在响应生理浓度的麻醉剂,1-氯-1,2,2-三氟环丁烷(F)时发生变化,但对结构相似的非诱导剂 1,2-二氯六氟环丁烷(F)则不会在人工膜和体外视网膜细胞系统中发生变化。膜偶极的调制提供了一种解释,可以克服与 GA 作用的替代膜介导机制相关的局限性。此外,通过将该技术与非侵入性视网膜成像技术相结合,我们提出该技术可以提供一种新的非侵入性技术来监测 GA 易感性并识别发生 AAGA 的风险患者。