School of Engineering, Brown University, Providence, Rhode Island.
Department of Biomedical Engineering, Kyung Hee University, Yongin, South Korea.
Biophys J. 2018 Oct 16;115(8):1481-1497. doi: 10.1016/j.bpj.2018.09.004. Epub 2018 Sep 13.
Over the past decade, optical methods have emerged for modulating brain functions as an alternative to electrical stimulation. Among various optical techniques, infrared neural stimulation has been effective via a thermal mechanism enabling focused and noninvasive stimulation without any genetic manipulation, but it results in bulk heating of neural tissue. Recently, it has been shown that neural cells can be activated more efficiently by pulsed near-infrared (NIR) light delivered to gold nanorods (GNRs) near the neural cells. Despite its potential, however, the biophysical mechanism underlying this GNR-enhanced NIR stimulation has not been clearly explained yet. Here, we propose an integrative and quantitative model to elucidate the mechanism by modeling heat generated from interaction between NIR light and GNRs, the temperature-dependent ion channels (transient receptor potential vanilloid 1; TRPV1) in the neuronal membrane, and a heat-induced capacitive current through the membrane. Our results show that NIR pulses induce abrupt temperature elevation near the neuronal membrane and lead to both the TRPV1-channel and capacitive currents. Both current sources synergistically increase the membrane potential and elicit an action potential, and which mechanism is dominant depends on conditions such as the laser pulse duration and TRPV1 channel density. Although the TRPV1 mechanism dominates in most cases we tested, the capacitive current makes a larger contribution when a very short laser pulse is illuminated on neural cells with relatively low TRPV1 channel densities.
在过去的十年中,光学方法已经作为电刺激的替代方法出现,用于调节大脑功能。在各种光学技术中,红外神经刺激通过热机制有效,能够实现聚焦和非侵入性刺激,而无需任何遗传操作,但它会导致神经组织的整体加热。最近,已经表明,通过将脉冲近红外(NIR)光递送至靠近神经细胞的金纳米棒(GNR),可以更有效地激活神经细胞。然而,尽管有这种潜力,但这种 GNR 增强的 NIR 刺激的生物物理机制尚未得到明确解释。在这里,我们提出了一个综合和定量的模型,通过模拟 NIR 光与 GNR 之间相互作用产生的热量、神经元膜中温度依赖性离子通道(瞬时受体电位香草酸 1;TRPV1)以及通过膜的热诱导电容电流,来阐明这种机制。我们的结果表明,NIR 脉冲会在神经元膜附近引起突然的温度升高,并导致 TRPV1 通道和电容电流。这两个电流源协同增加膜电位并引发动作电位,并且哪种机制占主导地位取决于激光脉冲持续时间和 TRPV1 通道密度等条件。虽然 TRPV1 机制在我们测试的大多数情况下占主导地位,但当用相对较低 TRPV1 通道密度的神经细胞照射非常短的激光脉冲时,电容电流的贡献更大。