A. R. Conde-Moro, F. Rocha-Almeida, E. Gebara, J. M. Delgado-García, C. Sandi, A. Gruart
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引用次数: 0
Abstract
Social behaviors such as cooperation are crucial for mammals. A deeper knowledge of the neuronal mechanisms underlying cooperation can be beneficial for people suffering from pathologies with impaired social behavior. Our aim was to study the brain activity when two animals synchronize their behavior to obtain a mutual reinforcement. In a previous work, we showed that the activity of the prelimbic cortex (PrL) was enhanced during cooperation in rats, especially in the ones leading most cooperative trials (leader rats). In this study, we investigated the specific cells in the PrL contributing to cooperative behaviors. To this end, we collected rats’ brains at key moments of the learning process to analyze the levels of c-FOS expression in the main cellular groups of the PrL. Leader rats showed increased c-FOS activity in cells expressing D1 receptors during cooperation. Besides, we analyzed the levels of anxiety, dominance, and locomotor behavior, finding that leader rats are in general less anxious and less dominant than followers. We also recorded local field potentials (LFPs) from the PrL, the nucleus accumbens septi (NAc), and the basolateral amygdala (BLA). A spectral analysis showed that delta activity in PrL and NAc increased when rats cooperated, while BLA activity in delta and theta bands decreased considerably during cooperation. The PrL and NAc also increased their connectivity in the high theta band during cooperation. Thus, the present work identifies the specific PrL cell types engaged in this behavior, as well as the way this information is propagated to selected downstream brain regions (BLA, NAc).
合作等社会行为对哺乳动物至关重要。深入了解合作背后的神经元机制,对患有社会行为受损病症的人来说是有益的。我们的目的是研究当两只动物同步其行为以获得相互强化时的大脑活动。在之前的研究中,我们发现大鼠在合作过程中前缘皮层(PrL)的活动会增强,尤其是在领导合作试验最多的大鼠(领导鼠)中。在这项研究中,我们调查了 PrL 中促成合作行为的特定细胞。为此,我们在学习过程的关键时刻采集了大鼠的大脑,分析了 PrL 主要细胞群中 c-FOS 的表达水平。在合作过程中,领头鼠表现出表达 D1 受体的细胞中 c-FOS 活性增加。此外,我们还分析了大鼠的焦虑程度、支配性和运动行为,发现领导者大鼠的焦虑程度和支配性普遍低于跟随者大鼠。我们还记录了PrL、隔核(NAc)和杏仁基底外侧(BLA)的局部场电位(LFPs)。频谱分析表明,当大鼠合作时,PrL和NAc的δ活动增加,而BLA的δ和θ波段活动在合作过程中大幅减少。在合作过程中,PrL和NAc在高θ波段的连接性也有所增加。因此,本研究确定了参与这种行为的特定 PrL 细胞类型,以及这种信息传播到选定下游脑区(BLA、NAc)的方式。
期刊介绍:
Cognitive Neurodynamics provides a unique forum of communication and cooperation for scientists and engineers working in the field of cognitive neurodynamics, intelligent science and applications, bridging the gap between theory and application, without any preference for pure theoretical, experimental or computational models.
The emphasis is to publish original models of cognitive neurodynamics, novel computational theories and experimental results. In particular, intelligent science inspired by cognitive neuroscience and neurodynamics is also very welcome.
The scope of Cognitive Neurodynamics covers cognitive neuroscience, neural computation based on dynamics, computer science, intelligent science as well as their interdisciplinary applications in the natural and engineering sciences. Papers that are appropriate for non-specialist readers are encouraged.
1. There is no page limit for manuscripts submitted to Cognitive Neurodynamics. Research papers should clearly represent an important advance of especially broad interest to researchers and technologists in neuroscience, biophysics, BCI, neural computer and intelligent robotics.
2. Cognitive Neurodynamics also welcomes brief communications: short papers reporting results that are of genuinely broad interest but that for one reason and another do not make a sufficiently complete story to justify a full article publication. Brief Communications should consist of approximately four manuscript pages.
3. Cognitive Neurodynamics publishes review articles in which a specific field is reviewed through an exhaustive literature survey. There are no restrictions on the number of pages. Review articles are usually invited, but submitted reviews will also be considered.