Quantifying tissue temperature changes induced by infrared neural stimulation: numerical simulation and MR thermometry.

IF 2.9 2区 医学 Q2 BIOCHEMICAL RESEARCH METHODS Biomedical optics express Pub Date : 2024-06-04 eCollection Date: 2024-07-01 DOI:10.1364/BOE.530854
Yinghua Xi, Kenneth E Schriver, Anna Wang Roe, Xiaotong Zhang
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Abstract

Infrared neural stimulation (INS) delivered via short pulse trains is an innovative tool that has potential for us use for studying brain function and circuitry, brain machine interface, and clinical use. The prevailing mechanism for INS involves the conversion of light energy into thermal transients, leading to neuronal membrane depolarization. Due to the potential risks of thermal damage, it is crucial to ensure that the resulting local temperature increases are within non-damaging limits for brain tissues. Previous studies have estimated damage thresholds using histological methods and have modeled thermal effects based on peripheral nerves. However, additional quantitative measurements and modeling studies are needed for the central nervous system. Here, we performed 7 T MRI thermometry on ex vivo rat brains following the delivery of infrared pulse trains at five different intensities from 0.1-1.0 J/cm2 (each pulse train 1,875 nm, 25 us/pulse, 200 Hz, 0.5 s duration, delivered through 200 µm fiber). Additionally, we utilized the General BioHeat Transfer Model (GBHTM) to simulate local temperature changes in perfused brain tissues while delivering these laser energies to tissue (with optical parameters of human skin) via three different sizes of optical fibers at five energy intensities. The simulation results clearly demonstrate that a 0.5 second INS pulse train induces an increase followed by an immediate drop in temperature at stimulation offset. The delivery of multiple pulse trains with 2.5 s interstimulus interval (ISI) leads to rising temperatures that plateau. Both thermometry and modeling results show that, using parameters that are commonly used in biological applications (200 µm diameter fiber, 0.1-1.0 J/cm2), the final temperature increase at the end of the 60 sec stimuli duration does not exceed 1°C with stimulation values of 0.1-0.5 J/cm2 and does not exceed 2°C with stimulation values of up to 1.0 J/cm2. Thus, the maximum temperature rise is consistent with the thermal damage threshold reported in previous studies. This study provides a quantitative evaluation of the temperature changes induced by INS, suggesting that existing practices pose minimal major safety concerns for biological tissues.

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量化红外神经刺激引起的组织温度变化:数值模拟和磁共振测温。
通过短脉冲序列传递的红外线神经刺激(INS)是一种创新工具,有望用于研究大脑功能和电路、脑机接口和临床应用。INS 的主要机制是将光能转化为热瞬态,从而导致神经元膜去极化。由于存在热损伤的潜在风险,确保所产生的局部温度升高在不损伤脑组织的范围内至关重要。以往的研究利用组织学方法估算了损伤阈值,并根据外周神经模拟了热效应。然而,还需要对中枢神经系统进行更多的定量测量和建模研究。在此,我们在体内大鼠脑部进行了 7 T MRI 测温,在此过程中,我们通过 200 µm 光纤传输了五种不同强度(0.1-1.0 J/cm2)的红外脉冲串(每个脉冲串 1,875 nm、25 us/脉冲、200 Hz、0.5 s 持续时间)。此外,我们还利用通用生物热传递模型(GBHTM)模拟了灌注脑组织的局部温度变化,同时在五种能量强度下通过三种不同尺寸的光纤将这些激光能量传递给组织(光学参数为人体皮肤)。模拟结果清楚地表明,0.5 秒的 INS 脉冲序列会引起温度升高,然后在刺激偏移时温度立即下降。以 2.5 秒刺激间隔(ISI)提供多个脉冲串会导致温度上升并趋于平稳。测温和建模结果都表明,使用生物应用中常用的参数(200 微米直径纤维、0.1-1.0 焦耳/平方厘米),刺激值为 0.1-0.5 焦耳/平方厘米时,60 秒刺激持续时间结束时的最终温度升高不超过 1°C,刺激值高达 1.0 焦耳/平方厘米时不超过 2°C。因此,最大温升与之前研究报告的热损伤阈值一致。这项研究对 INS 引起的温度变化进行了定量评估,表明现有做法对生物组织造成的重大安全问题微乎其微。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biomedical optics express
Biomedical optics express BIOCHEMICAL RESEARCH METHODS-OPTICS
CiteScore
6.80
自引率
11.80%
发文量
633
审稿时长
1 months
期刊介绍: The journal''s scope encompasses fundamental research, technology development, biomedical studies and clinical applications. BOEx focuses on the leading edge topics in the field, including: Tissue optics and spectroscopy Novel microscopies Optical coherence tomography Diffuse and fluorescence tomography Photoacoustic and multimodal imaging Molecular imaging and therapies Nanophotonic biosensing Optical biophysics/photobiology Microfluidic optical devices Vision research.
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