Boumhaouad Siham, Makowicz Emily A, Choi Sejoon, Bouhaddou Nezha, Balla Jihane, Taghzouti Khalid, Sulzer David, Mosharov Eugene V
Departments of Psychiatry and Neurology, Division of Molecular Therapeutics, New York State Psychiatric Institute, Columbia University Medical Center, New York, New York 10032, United States.
Physiology and Physiopathology Team, Genomics of Human Pathologies Research Center, Faculty of Sciences, Mohammed V University in Rabat, Rabat 10000, Morocco.
ACS Chem Neurosci. 2025 Feb 5;16(3):303-310. doi: 10.1021/acschemneuro.4c00323. Epub 2025 Jan 11.
Voluntary movement, motivation, and reinforcement learning depend on the activity of ventral midbrain neurons, which extend axons to release dopamine (DA) in the striatum. These neurons exhibit two patterns of action potential activity: low-frequency tonic activity that is intrinsically generated and superimposed high-frequency phasic bursts that are driven by synaptic inputs. acute striatal brain preparations are widely employed to study the regulation of evoked DA release but exhibit very different DA release kinetics than recordings. To investigate the relationship between phasic and tonic neuronal activity, we stimulated the slice in patterns intended to mimic tonic activity, which were interrupted by a series of burst stimuli. Conditioning the striatal slice with low-frequency activity altered DA release triggered by high-frequency bursts and produced kinetic parameters that resemble those . In the absence of applied tonic activity, nicotinic acetylcholine receptor and D2 DA receptor antagonists had no significant effect on neurotransmitter release, driven by repeated burst activity in the striatal brain slice. In contrast, in tonically stimulated slices, the D2 receptor blockade decreased the amount of DA released during a single-burst and facilitated DA release in subsequent bursts. This experimental system provides a means to reconcile the difference in the kinetics of DA release and and provides a novel approach to more accurately emulate pre- and postsynaptic mechanisms that control axonal DA release .
自主运动、动机和强化学习依赖于腹侧中脑神经元的活动,这些神经元延伸轴突以在纹状体中释放多巴胺(DA)。这些神经元表现出两种动作电位活动模式:内在产生的低频紧张性活动以及由突触输入驱动的叠加高频相位爆发。急性纹状体脑标本被广泛用于研究诱发DA释放的调节,但与记录相比表现出非常不同的DA释放动力学。为了研究相位和紧张性神经元活动之间的关系,我们以旨在模拟紧张性活动的模式刺激切片,这些模式被一系列爆发性刺激中断。用低频活动预处理纹状体切片会改变由高频爆发触发的DA释放,并产生类似于那些的动力学参数。在没有施加紧张性活动的情况下,烟碱型乙酰胆碱受体和D2 DA受体拮抗剂对纹状体脑切片中重复爆发活动驱动的神经递质释放没有显著影响。相比之下,在紧张性刺激的切片中,D2受体阻断减少了单次爆发期间释放的DA量,并促进了后续爆发中的DA释放。这个实验系统提供了一种调和DA释放动力学差异的方法,并提供了一种新的方法来更准确地模拟控制轴突DA释放的突触前和突触后机制。