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Basal forebrain projections to the lateral habenula modulate aggression reward

机译:基底前脑向外侧ha突投射可调节攻击性奖赏

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摘要

Maladaptive aggressive behaviour is associated with a number of neuropsychiatric disorders(1) and is thought to result partly from the inappropriate activation of brain reward systems in response to aggressive or violent social stimuli(2). Nuclei within the ventromedial hypothalamus(3-5), extended amygdala(6) and limbic(7) circuits are known to encode initiation of aggression; however, little is known about the neural mechanisms that directly modulate the motivational component of aggressive behaviour(8). Here we established a mouse model to measure the valence of aggressive inter-male social interaction with a smaller subordinate intruder as reinforcement for the development of conditioned place preference (CPP). Aggressors develop a CPP, whereas non-aggressors develop a conditioned place aversion to the intruder-paired context. Furthermore, we identify a functional GABAergic projection from the basal forebrain (BF) to the lateral habenula (lHb) that bi-directionally controls the valence of aggressive interactions. Circuit-specific silencing of GABAergic BF-lHb terminals of aggressors with halorhodopsin (NpHR3.0) increases lHb neuronal firing and abolishes CPP to the intruder-paired context. Activation of GABAergic BF-lHb terminals of non-aggressors with channelrhodopsin (ChR2) decreases lHb neuronal firing and promotes CPP to the intruder-paired context. Finally, we show that altering inhibitory transmission at BF-lHb terminals does not control the initiation of aggressive behaviour. These results demonstrate that the BF-lHb circuit has a critical role in regulating the valence of inter-male aggressive behaviour and provide novel mechanistic insight into the neural circuits modulating aggression reward processing.
机译:适应性攻击行为与许多神经精神疾病有关(1),并且被认为部分是由于对激进或暴力社交刺激做出不适当的大脑奖励系统激活所致(2)。已知腹内侧下丘脑(3-5),扁桃体(6)和边缘(7)回路中的核编码攻击的起始。然而,对于直接调节攻击性行为动机成分的神经机制知之甚少(8)。在这里,我们建立了一个小鼠模型来衡量与较小的下属入侵者之间积极的男性间社会互动的效价,以此来增强条件性位置偏好(CPP)的发展。侵略者发展了CPP,而非侵略者发展了对入侵者配对环境的有条件的地方厌恶。此外,我们确定了从基底前脑(BF)到侧ha(lHb)的功能性GABA能投影,该投影双向控制了积极相互作用的化合价。侵袭者的GABA能性BF-1Hb末端与视紫红质素(NpHR3.0)的电路特异性沉默增加了1Hb神经元放电并在入侵者配对的环境中废除了CPP。非侵袭者的GABA能BF-1Hb末端被通道视紫红质(ChR2)激活会降低1Hb神经元放电并促进CPP进入入侵者配对环境。最后,我们显示出改变BF-1Hb末端的抑制性传递不能控制攻击性行为的启动。这些结果表明,BF-1Hb回路在调节男性间侵略行为的效价方面起着关键作用,并为调节攻击性奖励过程的神经回路提供了新颖的机理见解。

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  • 来源
    《Nature》 |2016年第7609期|688-692|共5页
  • 作者单位

    Icahn Sch Med Mt Sinai, Fishberg Dept Neurosci, New York, NY 10029 USA|Icahn Sch Med Mt Sinai, Friedman Brain Inst, New York, NY 10029 USA|Icahn Sch Med Mt Sinai, Grad Program Neurosci, New York, NY 10029 USA;

    Icahn Sch Med Mt Sinai, Fishberg Dept Neurosci, New York, NY 10029 USA|Icahn Sch Med Mt Sinai, Friedman Brain Inst, New York, NY 10029 USA|Icahn Sch Med Mt Sinai, Grad Program Neurosci, New York, NY 10029 USA;

    Icahn Sch Med Mt Sinai, Fishberg Dept Neurosci, New York, NY 10029 USA|Icahn Sch Med Mt Sinai, Friedman Brain Inst, New York, NY 10029 USA|Icahn Sch Med Mt Sinai, Grad Program Neurosci, New York, NY 10029 USA;

    Stanford Univ, Med Ctr, Dept Psychiat & Behav Sci, Palo Alto, CA 94305 USA;

    Icahn Sch Med Mt Sinai, Fishberg Dept Neurosci, New York, NY 10029 USA|Icahn Sch Med Mt Sinai, Friedman Brain Inst, New York, NY 10029 USA|Icahn Sch Med Mt Sinai, Grad Program Neurosci, New York, NY 10029 USA;

    Icahn Sch Med Mt Sinai, Fishberg Dept Neurosci, New York, NY 10029 USA|Icahn Sch Med Mt Sinai, Friedman Brain Inst, New York, NY 10029 USA|Icahn Sch Med Mt Sinai, Grad Program Neurosci, New York, NY 10029 USA;

    Icahn Sch Med Mt Sinai, Fishberg Dept Neurosci, New York, NY 10029 USA|Icahn Sch Med Mt Sinai, Friedman Brain Inst, New York, NY 10029 USA;

    Icahn Sch Med Mt Sinai, Fishberg Dept Neurosci, New York, NY 10029 USA|Icahn Sch Med Mt Sinai, Friedman Brain Inst, New York, NY 10029 USA;

    Icahn Sch Med Mt Sinai, Pharmacol & Syst Therapeut, New York, NY 10029 USA|Icahn Sch Med Mt Sinai, Inst Syst Biomed, New York, NY 10029 USA;

    Icahn Sch Med Mt Sinai, Fishberg Dept Neurosci, New York, NY 10029 USA|Icahn Sch Med Mt Sinai, Friedman Brain Inst, New York, NY 10029 USA;

    Icahn Sch Med Mt Sinai, Fishberg Dept Neurosci, New York, NY 10029 USA|Icahn Sch Med Mt Sinai, Friedman Brain Inst, New York, NY 10029 USA;

    Icahn Sch Med Mt Sinai, Fishberg Dept Neurosci, New York, NY 10029 USA|Icahn Sch Med Mt Sinai, Friedman Brain Inst, New York, NY 10029 USA;

    Icahn Sch Med Mt Sinai, Fishberg Dept Neurosci, New York, NY 10029 USA|Icahn Sch Med Mt Sinai, Friedman Brain Inst, New York, NY 10029 USA;

    Icahn Sch Med Mt Sinai, Fishberg Dept Neurosci, New York, NY 10029 USA|Icahn Sch Med Mt Sinai, Friedman Brain Inst, New York, NY 10029 USA;

    Icahn Sch Med Mt Sinai, Fishberg Dept Neurosci, New York, NY 10029 USA|Icahn Sch Med Mt Sinai, Friedman Brain Inst, New York, NY 10029 USA|Icahn Sch Med Mt Sinai, Grad Program Neurosci, New York, NY 10029 USA;

    Icahn Sch Med Mt Sinai, Pharmacol & Syst Therapeut, New York, NY 10029 USA|Icahn Sch Med Mt Sinai, Inst Syst Biomed, New York, NY 10029 USA;

    Stanford Univ, Med Ctr, Dept Psychiat & Behav Sci, Palo Alto, CA 94305 USA;

    Icahn Sch Med Mt Sinai, Fishberg Dept Neurosci, New York, NY 10029 USA|Icahn Sch Med Mt Sinai, Friedman Brain Inst, New York, NY 10029 USA|Icahn Sch Med Mt Sinai, Pharmacol & Syst Therapeut, New York, NY 10029 USA|Icahn Sch Med Mt Sinai, Inst Syst Biomed, New York, NY 10029 USA;

    Icahn Sch Med Mt Sinai, Fishberg Dept Neurosci, New York, NY 10029 USA|Icahn Sch Med Mt Sinai, Friedman Brain Inst, New York, NY 10029 USA;

    Icahn Sch Med Mt Sinai, Fishberg Dept Neurosci, New York, NY 10029 USA|Icahn Sch Med Mt Sinai, Friedman Brain Inst, New York, NY 10029 USA;

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