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前扣带皮层在病理性攻击控制中的核心作用。

A central role for anterior cingulate cortex in the control of pathological aggression.

机构信息

Donders Institute for Brain, Cognition and Behaviour, Radboudumc, Nijmegen, the Netherlands; Department of Cognitive Neuroscience, Radboudumc, Nijmegen, the Netherlands.

Donders Institute for Brain, Cognition and Behaviour, Radboudumc, Nijmegen, the Netherlands; Department of Cognitive Neuroscience, Radboudumc, Nijmegen, the Netherlands.

出版信息

Curr Biol. 2021 Jun 7;31(11):2321-2333.e5. doi: 10.1016/j.cub.2021.03.062. Epub 2021 Apr 14.

Abstract

Controlling aggression is a crucial skill in social species like rodents and humans and has been associated with anterior cingulate cortex (ACC). Here, we directly link the failed regulation of aggression in BALB/cJ mice to ACC hypofunction. We first show that ACC in BALB/cJ mice is structurally degraded: neuron density is decreased, with pervasive neuron death and reactive astroglia. Gene-set enrichment analysis suggested that this process is driven by neuronal degeneration, which then triggers toxic astrogliosis. cFos expression across ACC indicated functional consequences: during aggressive encounters, ACC was engaged in control mice, but not BALB/cJ mice. Chemogenetically activating ACC during aggressive encounters drastically suppressed pathological aggression but left species-typical aggression intact. The network effects of our chemogenetic perturbation suggest that this behavioral rescue is mediated by suppression of amygdala and hypothalamus and activation of mediodorsal thalamus. Together, these findings highlight the central role of ACC in curbing pathological aggression.

摘要

控制攻击性是像啮齿动物和人类这样的社会性物种的关键技能,与前扣带皮层(ACC)有关。在这里,我们将 BALB/cJ 小鼠攻击行为的调节失败直接与 ACC 功能低下联系起来。我们首先表明,BALB/cJ 小鼠的 ACC 在结构上被破坏:神经元密度降低,广泛存在神经元死亡和反应性星形胶质细胞。基因集富集分析表明,这个过程是由神经元变性驱动的,随后引发毒性星形胶质细胞增生。整个 ACC 中的 cFos 表达表明存在功能后果:在攻击性行为中,ACC 在对照小鼠中被激活,但在 BALB/cJ 小鼠中未被激活。在攻击性行为中化学遗传激活 ACC 会极大地抑制病理性攻击行为,但不会影响物种典型的攻击行为。我们的化学遗传干扰的网络效应表明,这种行为挽救是通过抑制杏仁核和下丘脑以及激活中背侧丘脑来介导的。总之,这些发现强调了 ACC 在抑制病理性攻击行为中的核心作用。

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