Fisher Simon D, Robertson Paul B, Black Melony J, Redgrave Peter, Sagar Mark A, Abraham Wickliffe C, Reynolds John N J
Department of Anatomy and the Brain Health Research Centre, Brain Research New Zealand, University of Otago, Dunedin, 9054, New Zealand.
Laboratory for Animate Technologies, Auckland Bioengineering Institute, University of Auckland, Auckland, 1142, New Zealand.
Nat Commun. 2017 Aug 24;8(1):334. doi: 10.1038/s41467-017-00394-x.
Plasticity at synapses between the cortex and striatum is considered critical for learning novel actions. However, investigations of spike-timing-dependent plasticity (STDP) at these synapses have been performed largely in brain slice preparations, without consideration of physiological reinforcement signals. This has led to conflicting findings, and hampered the ability to relate neural plasticity to behavior. Using intracellular striatal recordings in intact rats, we show here that pairing presynaptic and postsynaptic activity induces robust Hebbian bidirectional plasticity, dependent on dopamine and adenosine signaling. Such plasticity, however, requires the arrival of a reward-conditioned sensory reinforcement signal within 2 s of the STDP pairing, thus revealing a timing-dependent eligibility trace on which reinforcement operates. These observations are validated with both computational modeling and behavioral testing. Our results indicate that Hebbian corticostriatal plasticity can be induced by classical reinforcement learning mechanisms, and might be central to the acquisition of novel actions.Spike timing dependent plasticity (STDP) has been studied extensively in slices but whether such pairings can induce plasticity in vivo is not known. Here the authors report an experimental paradigm that achieves bidirectional corticostriatal STDP in vivo through modulation by behaviourally relevant reinforcement signals, mediated by dopamine and adenosine signaling.
皮层与纹状体之间突触的可塑性被认为对学习新行为至关重要。然而,对这些突触处的尖峰时间依赖性可塑性(STDP)的研究大多是在脑片制备中进行的,并未考虑生理强化信号。这导致了相互矛盾的结果,并阻碍了将神经可塑性与行为联系起来的能力。我们在此使用完整大鼠的细胞内纹状体记录表明,配对突触前和突触后活动会诱导强大的赫布双向可塑性,这依赖于多巴胺和腺苷信号传导。然而,这种可塑性需要奖励条件性感觉强化信号在STDP配对的2秒内到达,从而揭示了强化作用所依赖的时间依赖性合格痕迹。这些观察结果通过计算建模和行为测试得到了验证。我们的结果表明,赫布皮质纹状体可塑性可由经典强化学习机制诱导,并且可能是获取新行为的核心。尖峰时间依赖性可塑性(STDP)已在切片中得到广泛研究,但这种配对是否能在体内诱导可塑性尚不清楚。在此,作者报告了一种实验范式,该范式通过行为相关强化信号的调节在体内实现双向皮质纹状体STDP,这种调节由多巴胺和腺苷信号传导介导。