A synaptic model for pain: Long-term potentiation in the anterior cingulate cortex

被引:0
作者
Zhuo, Min [1 ]
机构
[1] Univ Toronto, Dept Physiol, Fac Med, Ctr Study Pain, Toronto, ON M5S 1A8, Canada
关键词
adenylyl cyclases; anterior cingulate cortex; fear memory; gene knockout; immediate early genes; long-term depression; long-term potentiation; mice; persistent pain; synaptic plasticity;
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Investigation of molecular and cellular mechanisms of synaptic plasticity is the major focus of many neuroscientists. There are two major reasons for searching new genes and molecules contributing to central plasticity: first, it provides basic neural mechanism for learning and memory, a key function of the brain; second, it provides new targets for treating brain-related disease. Long-term potentiation (LTP), mostly intensely studies in the hippocampus and amygdala, is proposed to be a cellular model for learning and memory. Although it remains difficult to understand the roles of LTP in hippocampus-related memory, a role of LTP in fear, a simplified form of memory, has been established. Here, I will review recent cellular studies of LTP in the anterior cingulate cortex (ACC) and then compare studies in vivo and in vitro LTP by genetic/ pharmacological approaches. I propose that ACC LTP may serve as a cellular model for studying central sensitization that related to chronic pain, as well as pain-related cognitive emotional disorders. Understanding signaling pathways related to ACC LTP may help us to identify novel drug target for various mental disorders.
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页码:259 / 271
页数:13
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