Mandal Pravat K, Arora Yashika, Samkaria Avantika, Maroon Joseph C, Fodale Vincenzo, Mehta Yatin, Chang Yue-Fang
Neuroimaging and Neurospectroscopy (NINS) Laboratory, National Brain Research Centre, Gurgaon, India.
Department of Neurosurgery, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Cell Biochem Biophys. 2025 Jun;83(2):2281-2288. doi: 10.1007/s12013-024-01640-y. Epub 2024 Dec 18.
Glutathione (GSH) is a master antioxidant that counters oxidative stress. Clinical studies have confirmed significant depletion of GSH in the hippocampus and the substantia nigra as an early diagnostic biomarker for Alzheimer's disease (AD) and Parkinson disease (PD), respectively. External agents like anesthetics (inhaled and intravenous) have a different impact on GSH. There is significant depletion of the serum GSH peroxidase level after surgery with isoflurane anesthesia that is not found in patients administered intravenous propofol. The objective of this study is to evaluate the GSH level associated with isoflurane in vitro phantom model using non-invasive magnetic resonance (MR) spectroscopy and to detect residual isoflurane in a solution. MRS data was generated utilizing a 3T MR scanner (Prisma, Siemens) equipped with a 64-channel H head coil and dual tune (F/H) head coil. The GSH data acquisition was performed using the MEGA-PRESS pulse sequence using experimental parameters: ON = 4.40 ppm, OFF = 5.00 ppm, TE = 120 ms, TR = 2500 ms, voxel size = 25 × 25 × 25 mm and average = 32. Isoflurane was detected using F MRS studies using F/H head coil. GSH data was processed using KALPANA package and F data was processed using Siemens package. The GSH peak area (without isoflurane) in a phosphate-buffered solution (PBS) solution (control) showed a slow decline over time due to natural oxidation of GSH to dimeric glutathione (GSSG). On the contrary, the GSH peak area in similar model is reduced significantly (p = 0.016) due to isoflurane induced oxidation of GSH to GSSG compared to control. We also report a concise general method for data generation and processing of H MRS data for GSH as well as F monitoring platform using F MR spectroscopy. This is the first report wherein both H and F spectroscopy are applied to generate MRS data along with a unique data processing method. This method is highly sensitive and specifically detects GSH without ambiguity as well as isoflurane due to the unique chemical shift patterns of CF and CHF moieties. This non-invasive MRS approach is developed to monitor GSH-isoflurane interaction leading to oxidative stress and this approach can be extended for other inhaled anesthetics. This methodology using non-invasive F MR spectroscopy needs further development for future clinical studies.
谷胱甘肽(GSH)是一种主要的抗氧化剂,可对抗氧化应激。临床研究已证实,海马体和黑质中的GSH显著耗竭,分别作为阿尔茨海默病(AD)和帕金森病(PD)的早期诊断生物标志物。麻醉剂(吸入和静脉注射)等外部因素对GSH有不同影响。异氟烷麻醉术后血清GSH过氧化物酶水平显著降低,而静脉注射丙泊酚的患者未出现这种情况。本研究的目的是使用非侵入性磁共振(MR)波谱评估体外模型中与异氟烷相关的GSH水平,并检测溶液中的残留异氟烷。使用配备64通道H头线圈和双调谐(F/H)头线圈的3T MR扫描仪(西门子Prisma)生成MRS数据。使用MEGA-PRESS脉冲序列采集GSH数据,实验参数为:ON = 4.40 ppm,OFF = 5.00 ppm,TE = 120 ms,TR = 2500 ms,体素大小 = 25×25×25 mm,平均次数 = 32。使用F/H头线圈通过F MRS研究检测异氟烷。GSH数据使用KALPANA软件包处理,F数据使用西门子软件包处理。磷酸盐缓冲溶液(PBS)溶液(对照)中的GSH峰面积(无异氟烷)由于GSH自然氧化为二聚体谷胱甘肽(GSSG)而随时间缓慢下降。相反,与对照相比,由于异氟烷诱导GSH氧化为GSSG,类似模型中的GSH峰面积显著降低(p = 0.016)。我们还报告了一种简洁的通用方法,用于生成和处理用于GSH的H MRS数据以及使用F MR波谱的F监测平台。这是第一份同时应用H和F波谱生成MRS数据以及独特数据处理方法的报告。由于CF和CHF基团独特的化学位移模式,该方法高度灵敏,能够明确检测GSH以及异氟烷。开发这种非侵入性MRS方法是为了监测GSH - 异氟烷相互作用导致的氧化应激,并且这种方法可以扩展到其他吸入麻醉剂。这种使用非侵入性F MR波谱的方法需要进一步发展以用于未来的临床研究。