Gutlerner Johanna L, Penick Esther Chapin, Snyder Eric M, Kauer Julie A
Department of Molecular Pharmacology, Physiology, and Biotechnology, Brown University, Providence, RI 02912, USA.
Neuron. 2002 Dec 5;36(5):921-31. doi: 10.1016/s0896-6273(02)01051-6.
Dopamine neurons of the ventral tegmental area (VTA) are critically involved in processing novel and rewarding information, and mediate the addictive properties of many drugs of abuse. Excitatory synapses on these neurons, like those in other brain regions, exhibit long-term depression (LTD). Amphetamine or dopamine block LTD at VTA synapses, indicating that both pathological and local physiological stimuli regulate LTD. Here we show that in common with other forms of LTD, VTA LTD results from a selective decrease in AMPA receptor function accompanied by a decrease in cell surface AMPA receptors. However, unlike the case for any previously described form of LTD, activation of cyclic AMP-dependent protein kinase (PKA) is necessary and sufficient to trigger LTD at synapses on VTA dopamine neurons.
腹侧被盖区(VTA)的多巴胺神经元在处理新奇和奖励信息方面起着关键作用,并介导许多滥用药物的成瘾特性。与其他脑区的神经元一样,这些神经元上的兴奋性突触表现出长时程抑制(LTD)。安非他明或多巴胺可阻断VTA突触处的LTD,这表明病理刺激和局部生理刺激均可调节LTD。我们在此表明,与其他形式的LTD一样,VTA的LTD是由AMPA受体功能的选择性降低以及细胞表面AMPA受体数量的减少所致。然而,与之前描述的任何形式的LTD不同,环磷酸腺苷依赖性蛋白激酶(PKA)的激活对于触发VTA多巴胺神经元突触处的LTD而言是必要且充分的。