A hypothalamic-amygdala circuit underlying sexually dimorphic aggression.

IF 14.7 1区 医学 Q1 NEUROSCIENCES Neuron Pub Date : 2024-09-25 Epub Date: 2024-07-16 DOI:10.1016/j.neuron.2024.06.022
Zhenggang Zhu, Lu Miao, Kaiyuan Li, Qingqing Ma, Lina Pan, Chenjie Shen, Qianqian Ge, Yonglan Du, Luping Yin, Hongbin Yang, Xiaohong Xu, Ling-Hui Zeng, Yijun Liu, Han Xu, Xiao-Ming Li, Li Sun, Yan-Qin Yu, Shumin Duan
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Abstract

Male animals often display higher levels of aggression than females. However, the neural circuitry mechanisms underlying this sexually dimorphic aggression remain elusive. Here, we identify a hypothalamic-amygdala circuit that mediates male-biased aggression in mice. Specifically, the ventrolateral part of the ventromedial hypothalamus (VMHvl), a sexually dimorphic region associated with eliciting male-biased aggression, projects densely to the posterior substantia innominata (pSI), an area that promotes similar levels of attack in both sexes of mice. Although the VMHvl innervates the pSI unidirectionally through both excitatory and inhibitory connections, it is the excitatory VMHvl-pSI projections that are strengthened in males to promote aggression, whereas the inhibitory connections that reduce aggressive behavior are strengthened in females. Consequently, the convergent hypothalamic input onto the pSI leads to heightened pSI activity in males, resulting in male-biased aggression. Our findings reveal a sexually distinct excitation-inhibition balance of a hypothalamic-amygdala circuit that underlies sexually dimorphic aggression.

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下丘脑-杏仁核回路是性双态攻击行为的基础。
雄性动物通常比雌性动物表现出更高水平的攻击性。然而,这种性别二态攻击性的神经回路机制仍然难以捉摸。在这里,我们发现了一个介导小鼠雄性攻击行为的下丘脑-杏仁核回路。具体来说,下丘脑腹内侧的腹外侧部分(VMHvl)是一个与诱发雄性偏向攻击性相关的性双态区域,它密集地投射到小鼠的后腹内实质(pSI),而该区域在两种性别的小鼠中都能促进相似水平的攻击。虽然 VMHvl 通过兴奋性和抑制性连接单向支配 pSI,但在雄性小鼠中,VMHvl-pSI 的兴奋性投射得到加强,从而促进攻击行为,而在雌性小鼠中,抑制性连接得到加强,从而减少攻击行为。因此,下丘脑对 pSI 的会聚输入会导致男性的 pSI 活动增强,从而产生男性偏好的攻击行为。我们的研究结果揭示了下丘脑-杏仁核回路在兴奋-抑制平衡方面的性别差异,而这正是性别二态攻击行为的基础。
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来源期刊
Neuron
Neuron 医学-神经科学
CiteScore
24.50
自引率
3.10%
发文量
382
审稿时长
1 months
期刊介绍: Established as a highly influential journal in neuroscience, Neuron is widely relied upon in the field. The editors adopt interdisciplinary strategies, integrating biophysical, cellular, developmental, and molecular approaches alongside a systems approach to sensory, motor, and higher-order cognitive functions. Serving as a premier intellectual forum, Neuron holds a prominent position in the entire neuroscience community.
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