Department of Pharmacology, University of Maryland School of Medicine, Baltimore, Maryland.
Eating and Addiction Section, National Institute of Digestive and Diabetes and Kidney Diseases, Bethesda, Maryland.
Biol Psychiatry. 2018 Jun 15;83(12):1012-1023. doi: 10.1016/j.biopsych.2018.01.003. Epub 2018 Jan 12.
The ability to appropriately integrate and respond to rewarding and aversive stimuli is essential for survival. The ventral pallidum (VP) plays a critical role in processing both rewarding and aversive stimuli. However, the VP is a heterogeneous structure, and how VP subpopulations integrate into larger reward networks to ultimately modulate these behaviors is not known. We identify a noncanonical population of glutamatergic VP neurons that play a unique role in responding to aversive stimuli and constraining inappropriate reward seeking.
Using neurochemical, genetic, and electrophysiological approaches, we characterized glutamatergic VP neurons (n = 4-8 mice/group). We performed patch clamp and in vivo electrophysiology recordings in the lateral habenula, rostromedial tegmental nucleus, and ventral tegmental area to determine the effect of glutamatergic VP neuron activation in these target regions (n = 6-10 mice/group). Finally, we selectively optogenetically stimulated glutamatergic VP neurons in a real-time place preference task and ablated these neurons using a virally expressed caspase to determine their necessity for reward seeking.
Glutamatergic VP neurons exhibit little overlap with cholinergic or gamma-aminobutyric acidergic markers, the canonical VP subtypes, and exhibit distinct membrane properties. Glutamatergic VP neurons innervate and increase firing activity of the lateral habenula, rostromedial tegmental nucleus, and gamma-aminobutyric acidergic ventral tegmental area neurons. While nonselective optogenetic stimulation of the VP induced a robust place preference, selective activation of glutamatergic VP neurons induced a place avoidance. Viral ablation of glutamatergic VP neurons increased reward responding and abolished taste aversion to sucrose.
Glutamatergic VP neurons constitute a noncanonical subpopulation of VP neurons. These glutamatergic VP neurons increase activity of the lateral habenula, rostromedial tegmental nucleus, and gamma-aminobutyric acidergic ventral tegmental area neurons and adaptively constrain reward seeking.
适当整合和响应奖赏性和厌恶性刺激的能力对生存至关重要。腹侧苍白球(VP)在处理奖赏性和厌恶性刺激方面起着关键作用。然而,VP 是一个异质结构,VP 亚群如何整合到更大的奖励网络中,最终调节这些行为尚不清楚。我们发现了一个非典型的 VP 谷氨酸能神经元群体,它在对厌恶性刺激做出反应和限制不当的奖励寻求方面发挥着独特的作用。
使用神经化学、遗传和电生理方法,我们对 VP 谷氨酸能神经元(每组 n=4-8 只小鼠)进行了特征描述。我们在外侧缰核、中脑腹侧被盖区和腹侧被盖区进行了膜片钳和体内电生理学记录,以确定 VP 谷氨酸能神经元激活对这些靶区的影响(每组 n=6-10 只小鼠)。最后,我们在实时位置偏好任务中选择性地光遗传学刺激 VP 谷氨酸能神经元,并使用表达半胱天冬酶的病毒对这些神经元进行消融,以确定它们对奖励寻求的必要性。
VP 谷氨酸能神经元与胆碱能或γ-氨基丁酸能标记物、经典的 VP 亚型几乎没有重叠,表现出独特的膜特性。VP 谷氨酸能神经元支配并增加外侧缰核、中脑腹侧被盖区和 GABA 能腹侧被盖区神经元的放电活动。虽然 VP 的非选择性光遗传学刺激诱导了强烈的位置偏好,但 VP 谷氨酸能神经元的选择性激活诱导了位置回避。VP 谷氨酸能神经元的病毒消融增加了奖励反应,并消除了对蔗糖的味觉厌恶。
VP 谷氨酸能神经元构成了 VP 神经元的一个非典型亚群。这些 VP 谷氨酸能神经元增加了外侧缰核、中脑腹侧被盖区和 GABA 能腹侧被盖区神经元的活动,并适应性地限制了奖励寻求。