Instituto de Fisica, Universidad Nacional Autonoma de Mexico, Mexico City, Mexico.
Department of Psychiatry, School of Medicine, Washington University, St. Louis, Missouri, USA.
Ultrasound Med Biol. 2020 Aug;46(8):2044-2056. doi: 10.1016/j.ultrasmedbio.2020.04.004. Epub 2020 May 29.
Studies in animal models have revealed that long exposures to anesthetics can induce apoptosis in the newborn and young developing brain. These effects have not been confirmed in humans because of the lack of a non-invasive, practical in vivo imaging tool with the ability to detect these changes. Following the successful use of ultrasound backscatter spectroscopy (UBS) to monitor in vivo cell death in breast tumors, we aimed to use UBS to assess the neurotoxicity of the anesthetic sevoflurane (SEVO) in a non-human primate (NHP) model. Sixteen 2- to 7-day-old rhesus macaques were exposed for 5 h to SEVO. Ultrasound scanning was done with a phased array transducer on a clinical ultrasound scanner operated at 10 MHz. Data consisting of 10-15 frames of radiofrequency (RF) echo signals from coronal views of the thalamus were obtained 0.5 and 6.0 h after initiating exposure. The UBS parameter "effective scatterer size" (ESS) was estimated by fitting a scattering form factor (FF) model to the FF measured from RF echo signals. The approach involved analyzing the frequency dependence of the measured FF to characterize scattering sources and selecting the FF model based on a χ goodness-of-fit criterion. To assess data quality, a rigorous acceptance criterion based on the analysis of prevalence of diffuse scattering (an assumption in the estimation of ESS) was established. ESS changes after exposure to SEVO were compared with changes in a control group of five primates for which ultrasound data were acquired at 0 and 10 min (no apoptosis expected). Over the entire data set, the average measured FF at 0.5 and 6.0 h monotonically decreased with frequency, justifying fitting a single FF over the analysis bandwidth. χ values of a (inhomogeneous continuum) Gaussian FF model were one-fifth those of the discrete fluid sphere model, suggesting that a continuum scatterer model better represents ultrasound scattering in the young rhesus brain. After application of the data quality criterion, only 5 of 16 subjects from the apoptotic group and 5 of 5 subjects from the control group fulfilled the acceptance criteria. All subjects in the apoptotic group that passed the acceptance criterion exhibited a significant ESS reduction at 6.0 h. These changes (-6.4%, 95% Interquartile Range: -14.3% to -3.3%) were larger than those in the control group (-0.8%, 95% Interquartile Range: -2.0% to 1.5%]). Data with a low prevalence of diffuse scattering corresponded to possibly biased results. Thus, ESS has the potential to detect changes in brain microstructure related to anesthesia-induced apoptosis.
在动物模型中的研究表明,长时间暴露于麻醉剂会诱导新生和发育中大脑的细胞凋亡。由于缺乏一种能够检测到这些变化的非侵入性、实用的体内成像工具,这些影响在人类中尚未得到证实。在成功使用超声背散射光谱(UBS)监测乳腺肿瘤体内细胞死亡之后,我们旨在使用 UBS 评估麻醉剂七氟醚(SEVO)在非人类灵长类动物(NHP)模型中的神经毒性。将 16 只 2 至 7 天大的恒河猴暴露于 SEVO 中 5 小时。使用临床超声扫描仪上的相控阵换能器以 10 MHz 的频率进行超声扫描。在开始暴露后 0.5 和 6.0 小时,从丘脑冠状视图获得由 10-15 个射频(RF)回波信号帧组成的数据。通过将散射形式因子(FF)模型拟合到从 RF 回波信号测量的 FF 来估计 UBS 参数“有效散射体尺寸”(ESS)。该方法涉及分析所测量的 FF 的频率依赖性,以表征散射源,并根据 χ 拟合优度准则选择 FF 模型。为了评估数据质量,根据弥散散射的普遍性分析(在 ESS 估计中是一个假设)建立了严格的接受标准。与超声数据在 0 和 10 分钟(无细胞凋亡预期)时采集的对照组的五只灵长类动物相比,SEVO 暴露后 ESS 的变化。在整个数据集上,在 0.5 和 6.0 小时时,平均测量的 FF 随频率单调下降,证明在分析带宽上拟合单个 FF 是合理的。(不均匀连续体)高斯 FF 模型的 χ 值是离散流体球模型的五分之一,表明连续体散射模型更能代表年轻恒河猴大脑中的超声散射。在应用数据质量标准之后,只有凋亡组的 16 个研究对象中的 5 个和对照组的 5 个研究对象符合接受标准。通过接受标准的凋亡组的所有研究对象在 6.0 小时时均显示出 ESS 明显降低。这些变化(-6.4%,95% 四分位距:-14.3%至-3.3%)大于对照组(-0.8%,95% 四分位距:-2.0%至 1.5%])。具有低弥散散射普遍性的数据对应于可能存在偏差的结果。因此,ESS 有可能检测到与麻醉诱导的细胞凋亡相关的脑微观结构变化。