Department of Pharmacology and Toxicology, University at Buffalo, Buffalo, New York 14214
Department of Pharmacology and Toxicology, University at Buffalo, Buffalo, New York 14214.
J Neurosci. 2019 Dec 11;39(50):10071-10080. doi: 10.1523/JNEUROSCI.1005-19.2019. Epub 2019 Nov 8.
The claustrum connects with a broad range of cortical areas including the prefrontal cortex (PFC). However, the function of the claustrum (CLA) and its neural projections remains largely unknown. Here, we elucidated the role of the neural projections from the CLA to the PFC in regulating impulsivity in male rats. We first identified the CLA-PFC pathway by retrograde tracer and virus expression. By using immunofluorescent staining of the c-Fos-positive neurons, we showed that chemogenetic activation and inhibition of the CLA-PFC pathway reduced and increased overall activity of the PFC, respectively. In the 5-choice serial reaction time task (5-CSRTT), we found that chemogenetic activation and inhibition of the CLA-PFC pathway increased and reduced the impulsive-like behavior (i.e., premature responses), respectively. Furthermore, chemogenetic inhibition of the CLA-PFC pathway prevented methamphetamine-induced impulsivity, without affecting methamphetamine-induced hyperactivity. In contrast to the role of CLA-PFC pathway in selectively regulating impulsivity, activation of the claustrum disrupted attention in the 5-CSRTT. These results indicate that the CLA-PFC pathway is essential for impulsivity. This study may shed light on the understanding of impulsivity-related disorders such as drug addiction. The claustrum is one of the most mysterious brain regions. Although extensive anatomical studies demonstrated that the claustrum connects with many cortical areas, the function of the neural projections between the claustrum and cortical areas remain largely unknown. Here, we showed that the neural projections from the claustrum to the prefrontal cortex regulates impulsivity by using the designer drugs (DREADDs)-based chemogenetic tools. Interestingly, the claustrum-prefrontal cortex pathway also regulates methamphetamine-induced impulsivity, suggesting a critical role of this neural pathway in regulating impulsivity-related disorders such as drug addiction. Our results provided preclinical evidence that the claustrum-prefrontal cortex regulates impulsivity. The claustrum-prefrontal cortex pathway may be a novel target for the treatment of impulsivity-related brain disorders.
屏状核与包括前额叶皮层(PFC)在内的广泛皮质区域相连。然而,屏状核(CLA)及其神经投射的功能在很大程度上仍然未知。在这里,我们阐明了 CLA 投射到 PFC 的神经投射在调节雄性大鼠冲动性中的作用。我们首先通过逆行示踪剂和病毒表达鉴定了 CLA-PFC 通路。通过对 c-Fos 阳性神经元的免疫荧光染色,我们显示化学遗传激活和抑制 CLA-PFC 通路分别减少和增加了 PFC 的整体活动。在 5 选择序列反应时间任务(5-CSRTT)中,我们发现化学遗传激活和抑制 CLA-PFC 通路分别增加和减少冲动样行为(即过早反应)。此外,化学遗传抑制 CLA-PFC 通路可预防安非他命引起的冲动性,而不影响安非他命引起的多动。与 CLA-PFC 通路在选择性调节冲动性中的作用相反,CLA 的激活破坏了 5-CSRTT 中的注意力。这些结果表明 CLA-PFC 通路对于冲动性是必不可少的。这项研究可能有助于理解与冲动性相关的疾病,如药物成瘾。屏状核是大脑最神秘的区域之一。尽管广泛的解剖学研究表明屏状核与许多皮质区域相连,但屏状核和皮质区域之间的神经投射的功能在很大程度上仍然未知。在这里,我们使用基于设计药物(DREADDs)的化学遗传工具表明,来自屏状核到前额叶皮层的神经投射通过调节冲动性。有趣的是,CLA-PFC 通路也调节安非他命引起的冲动性,表明该神经通路在调节冲动性相关疾病(如药物成瘾)中起着关键作用。我们的结果提供了临床前证据,表明 CLA-PFC 调节冲动性。CLA-PFC 通路可能是治疗与冲动性相关的大脑疾病的新靶点。