Zhong Ling, Brown Joshua, Kramer Audra, Kaleka Kanwardeep, Petersen Amber, Krueger Jamie N, Florence Matthew, Muelbl Matthew J, Battle Michelle, Murphy Geoffrey G, Olsen Christopher M, Gerges Nashaat Z
Departments of Cell Biology, Neurobiology and Anatomy, Neuroscience Research Center, and.
Molecular & Behavioral Neuroscience Institute and.
J Neurosci. 2015 May 13;35(19):7503-8. doi: 10.1523/JNEUROSCI.0274-15.2015.
Increasing plasticity in neurons of the prefrontal cortex (PFC) has been proposed as a possible therapeutic tool to enhance extinction, a process that is impaired in post-traumatic stress disorder, schizophrenia, and addiction. To test this hypothesis, we generated transgenic mice that overexpress neurogranin (a calmodulin-binding protein that facilitates long-term potentiation) in the PFC. Neurogranin overexpression in the PFC enhanced long-term potentiation and increased the rates of extinction learning of both fear conditioning and sucrose self-administration. Our results indicate that elevated neurogranin function within the PFC can enhance local plasticity and increase the rate of extinction learning across different behavioral tasks. Thus, neurogranin can provide a molecular link between enhanced plasticity and enhanced extinction.
前额叶皮层(PFC)神经元可塑性的增强已被提议作为一种可能的治疗手段,以增强消退作用,这一过程在创伤后应激障碍、精神分裂症和成瘾中会受到损害。为了验证这一假设,我们构建了在前额叶皮层中过表达神经颗粒素(一种促进长时程增强的钙调蛋白结合蛋白)的转基因小鼠。前额叶皮层中神经颗粒素的过表达增强了长时程增强,并提高了恐惧条件反射和蔗糖自我给药的消退学习速率。我们的结果表明,前额叶皮层内神经颗粒素功能的增强可增强局部可塑性,并提高不同行为任务的消退学习速率。因此,神经颗粒素可在增强的可塑性和增强的消退之间提供分子联系。