Lopez-Castro Alejandra, Angeles-Valdez Diego, Rojas-Piloni Gerardo, Garza-Villarreal Eduardo A
Instituto de Neurobiología, Universidad Nacional Autónoma de México, Querétaro, Mexico.
Department of Biomedical Sciences of Cells and Systems, Cognitive Neuroscience Center, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.
Front Neurosci. 2022 Sep 29;16:945594. doi: 10.3389/fnins.2022.945594. eCollection 2022.
Neuromodulation interventions, such as Deep Brain Stimulation (DBS) and repeated transcranial magnetic stimulation (rTMS), are proposed as possible new complementary therapies to treat substance use disorders (SUD) such as alcohol use disorder (AUD). It is hypothesized that neuromodulation may induce neural plasticity in the reward and frontostriatal systems electrical field induction, possibly reducing symptoms. Preclinical self-administration rodent models of AUD may help us gain insight into the effects of neuromodulation therapies on different pathology, as well as the neural mechanisms behind the positive effects. DBS, or any type of brain stimulation using intracranial electrodes in rodents, would benefit from the use of magnetic resonance imaging (MRI) to study the longitudinal effects and mechanisms of stimulation as well as novel targets, as it is a non-invasive technique that allows the analysis of structural and functional changes in the brain. To do this, there is a need for MRI-compatible electrodes that allow for MRI acquisition with minimal distortion of the magnetic field. In this protocol, we present a method for the construction and surgery of chronically implantable monopolar carbon electrodes for use in rats. Unlike conventional electrodes, carbon electrodes are resistant to high temperatures, flexible, and generate fewer artifacts in MRI compared to conventional ones. We validated its use by using a focal electrical stimulation high-frequency (20 Hz) protocol that lasted ∼10 sessions. We propose that this technique can also be used for the research of the neurophysiological bases of the neuromodulatory treatment in other preclinical substance use disorders (SUD) models.
神经调节干预措施,如深部脑刺激(DBS)和重复经颅磁刺激(rTMS),被提议作为治疗酒精使用障碍(AUD)等物质使用障碍(SUD)的可能的新辅助疗法。据推测,神经调节可能通过电场诱导在奖赏和前额叶纹状体系统中诱导神经可塑性,从而可能减轻症状。酒精使用障碍的临床前自我给药啮齿动物模型可能有助于我们深入了解神经调节疗法对不同病理的影响,以及积极效果背后的神经机制。DBS或在啮齿动物中使用颅内电极的任何类型的脑刺激,将受益于使用磁共振成像(MRI)来研究刺激的纵向效应和机制以及新的靶点,因为它是一种非侵入性技术,可以分析大脑的结构和功能变化。为此,需要与MRI兼容的电极,以便在磁场最小失真的情况下进行MRI采集。在本方案中,我们介绍了一种用于大鼠的可长期植入的单极碳电极的构建和手术方法。与传统电极不同,碳电极耐高温、柔韧性好,并且在MRI中产生的伪影比传统电极少。我们通过使用持续约10次的局灶性高频(20 Hz)电刺激方案验证了其用途。我们提出,该技术也可用于研究其他临床前物质使用障碍(SUD)模型中神经调节治疗的神经生理基础。