Constraints on the subsecond modulation of striatal dynamics by physiological dopamine signaling

IF 21.2 1区 医学 Q1 NEUROSCIENCES
Charltien Long, Kwang Lee, Long Yang, Theresia Dafalias, Alexander K. Wu, Sotiris C. Masmanidis
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Abstract

Dopaminergic neurons play a crucial role in associative learning, but their capacity to regulate behavior on subsecond timescales remains debated. It is thought that dopaminergic neurons drive certain behaviors by rapidly modulating striatal spiking activity; however, a view has emerged that only artificially high (that is, supra-physiological) dopamine signals alter behavior on fast timescales. This raises the possibility that moment-to-moment striatal spiking activity is not strongly shaped by dopamine signals in the physiological range. To test this, we transiently altered dopamine levels while monitoring spiking responses in the ventral striatum of behaving mice. These manipulations led to only weak changes in striatal activity, except when dopamine release exceeded reward-matched levels. These findings suggest that dopaminergic neurons normally play a minor role in the subsecond modulation of striatal dynamics in relation to other inputs and demonstrate the importance of discerning dopaminergic neuron contributions to brain function under physiological and potentially nonphysiological conditions.

Abstract Image

生理多巴胺信号对纹状体动力学亚秒级调控的制约因素
多巴胺能神经元在联想学习中起着至关重要的作用,但它们在亚秒级时间尺度上调节行为的能力仍存在争议。一般认为,多巴胺能神经元通过快速调节纹状体的尖峰活动来驱动某些行为;但也有一种观点认为,只有人为的高水平(即超生理水平)多巴胺信号才能在快速时间尺度上改变行为。这就提出了一种可能性,即在生理范围内,纹状体尖峰活动并不会受到多巴胺信号的强烈影响。为了验证这一点,我们在监测行为小鼠腹侧纹状体尖峰反应的同时,瞬时改变了多巴胺水平。除了当多巴胺释放量超过奖赏匹配水平时,这些操作只会导致纹状体活动发生微弱变化。这些研究结果表明,多巴胺能神经元通常在纹状体动态的亚秒级调控中扮演着相对于其他输入的次要角色,并证明了在生理和潜在的非生理条件下辨别多巴胺能神经元对大脑功能贡献的重要性。
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来源期刊
Nature neuroscience
Nature neuroscience 医学-神经科学
CiteScore
38.60
自引率
1.20%
发文量
212
审稿时长
1 months
期刊介绍: Nature Neuroscience, a multidisciplinary journal, publishes papers of the utmost quality and significance across all realms of neuroscience. The editors welcome contributions spanning molecular, cellular, systems, and cognitive neuroscience, along with psychophysics, computational modeling, and nervous system disorders. While no area is off-limits, studies offering fundamental insights into nervous system function receive priority. The journal offers high visibility to both readers and authors, fostering interdisciplinary communication and accessibility to a broad audience. It maintains high standards of copy editing and production, rigorous peer review, rapid publication, and operates independently from academic societies and other vested interests. In addition to primary research, Nature Neuroscience features news and views, reviews, editorials, commentaries, perspectives, book reviews, and correspondence, aiming to serve as the voice of the global neuroscience community.
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