Focused Ultrasound modulates dopamine in a mesolimbic reward circuit

bioRxiv Pub Date : 2024-02-14 DOI:10.1101/2024.02.13.580202
Greatness O. Olaitan, Mallikarjunarao Ganesana, Wendy J. Lynch, W. Legon, B. Venton
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Abstract

Dopamine is a neurotransmitter that plays a significant role in reward and motivation. Dysfunction in the mesolimbic dopamine pathway has been linked to a variety of psychiatric disorders, including addiction. Low-intensity focused ultrasound (LIFU) has demonstrated effects on brain activity, but how LIFU affects dopamine neurotransmission is not known. Here, we applied three different intensities (6.5, 13, and 26 W/cm2 Isppa) of 2-minute LIFU to the prelimbic region (PLC) and measured dopamine in the nucleus accumbens (NAc) core using fast-scan cyclic voltammetry. Two minutes of LIFU sonication at 13 W/cm2 to the PLC significantly reduced dopamine release by ∼ 50% for up to 2 hours. However, double the intensity (26 W/cm2) resulted in less inhibition (∼30%), and half the intensity (6.5 W/cm2) did not result in any inhibition of dopamine. Anatomical controls applying LIFU to the primary somatosensory cortex did not change NAc core dopamine, and applying LIFU to the PLC did not affect dopamine release in the caudate or NAc shell. Histological evaluations showed no evidence of cell damage or death. Modeling of temperature rise demonstrates a maximum temperature change of 0.5°C with 13 W/cm2, suggesting that modulation is not due to thermal mechanisms. These studies show that LIFU at a moderate intensity provides a noninvasive, high spatial resolution means to modulate specific mesolimbic circuits that could be used in future studies to target and repair pathways that are dysfunctional in addiction and other psychiatric diseases.
聚焦超声调节中边缘奖赏回路中的多巴胺
多巴胺是一种神经递质,在奖赏和动机方面发挥着重要作用。间叶多巴胺通路的功能障碍与包括成瘾在内的多种精神疾病有关。低强度聚焦超声(LIFU)已证明对大脑活动有影响,但低强度聚焦超声如何影响多巴胺神经递质尚不清楚。在这里,我们在前边缘区(PLC)应用了三种不同强度(6.5、13 和 26 W/cm2 Isppa)的 2 分钟 LIFU,并使用快速扫描循环伏安法测量了脑核(NAc)核心的多巴胺。以 13 瓦/平方厘米的功率对 PLC 进行两分钟的 LIFU 超声处理,可在长达 2 小时的时间内显著减少多巴胺释放 50%。然而,双倍强度(26 W/cm2)的抑制作用较小(∼30%),而一半强度(6.5 W/cm2)的多巴胺抑制作用则不明显。对初级躯体感觉皮层施加 LIFU 的解剖学对照没有改变 NAc 核心多巴胺,对 PLC 施加 LIFU 也没有影响尾状核或 NAc 外壳的多巴胺释放。组织学评估显示,没有细胞受损或死亡的迹象。温度上升模型显示,13 W/cm2 的最大温度变化为 0.5°C,这表明调节并非由热机制引起。这些研究表明,中等强度的 LIFU 提供了一种非侵入性、高空间分辨率的方法来调节特定的间叶环路,可用于未来的研究中,靶向修复成瘾和其他精神疾病中功能失调的通路。
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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