Shin Jung Hoon, Adrover Martín F, Wess Jürgen, Alvarez Veronica A
National Institute on Alcohol Abuse and Alcoholism, NIH, Bethesda, MD 20892;
National Institute of Diabetes and Digestive and Kidney Diseases, NIH, Bethesda, MD 20892.
Proc Natl Acad Sci U S A. 2015 Jun 30;112(26):8124-9. doi: 10.1073/pnas.1508846112. Epub 2015 Jun 15.
Cholinergic transmission in the striatum functions as a key modulator of dopamine (DA) transmission and synaptic plasticity, both of which are required for reward and motor learning. Acetylcholine (ACh) can elicit striatal DA release through activation of nicotinic ACh receptors (nAChRs) on DA axonal projections. However, it remains controversial how muscarinic ACh receptors (mAChRs) modulate striatal DA release, with studies reporting both potentiation and depression of striatal DA transmission by mAChR agonists. This study investigates the mAChR-mediated regulation of release from three types of midbrain neurons that project to striatum: DA, DA/glutamate, and glutamate neurons. We found that M5 mAChRs potentiate DA and glutamate release only from DA and DA/glutamate projections from the midbrain. We also show that M2/M4 mAChRs depress the nAChR-dependent mechanism of DA release in the striatum. These results suggest that M5 receptors on DA neuron terminals enhance DA release, whereas M2/M4 autoreceptors on cholinergic terminals inhibit ACh release and subsequent nAChR-dependent DA release. Our findings clarify the mechanisms of mAChR-dependent modulation of DA and glutamate transmission in the striatum.
纹状体中的胆碱能传递作为多巴胺(DA)传递和突触可塑性的关键调节因子,这两者都是奖励和运动学习所必需的。乙酰胆碱(ACh)可通过激活DA轴突投射上的烟碱型ACh受体(nAChRs)来引发纹状体DA释放。然而,毒蕈碱型ACh受体(mAChRs)如何调节纹状体DA释放仍存在争议,研究报告显示mAChR激动剂对纹状体DA传递既有增强作用又有抑制作用。本研究调查了mAChR介导的从投射到纹状体的三种类型中脑神经元释放的调节:DA、DA/谷氨酸和谷氨酸神经元。我们发现M5 mAChRs仅增强来自中脑的DA和DA/谷氨酸投射的DA和谷氨酸释放。我们还表明,M2/M4 mAChRs抑制纹状体中DA释放的nAChR依赖性机制。这些结果表明,DA神经元终末上的M5受体增强DA释放,而胆碱能终末上的M2/M4自身受体抑制ACh释放及随后的nAChR依赖性DA释放。我们的研究结果阐明了mAChR依赖性调节纹状体中DA和谷氨酸传递的机制。