Parabrachial CGRP Neurons Establish and Sustain Aversive Taste Memories

被引:93
|
作者
Chen, Jane Y. [1 ,2 ,3 ,4 ]
Campos, Carlos A. [1 ,2 ,3 ]
Jarvie, Brooke C. [1 ,2 ,3 ,4 ]
Palmiter, Richard D. [1 ,2 ,3 ]
机构
[1] Univ Washington, Howard Hughes Med Inst, Seattle, WA 98195 USA
[2] Univ Washington, Dept Biochem, Seattle, WA 98195 USA
[3] Univ Washington, Dept Genome Sci, Seattle, WA 98195 USA
[4] Univ Washington, Grad Program Neurosci, Seattle, WA 98195 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
BED NUCLEUS; STRIA TERMINALIS; NEURAL CIRCUIT; AMYGDALA; LESIONS; MECHANISMS; ARC/ARG3.1; INDUCTION; PAIN;
D O I
10.1016/j.neuron.2018.09.032
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Food aversions develop when the taste of a novel food is associated with sickness, which often occurs after food poisoning or chemotherapy treatment. We identified calcitonin-gene-related peptide (CGRP) neurons in the parabrachial nucleus (PBN) as sufficient and necessary for establishing a conditioned taste aversion (CTA). Photoactivating projections from CGRP (PBN )neurons to either the central nucleus of the amygdala or the bed nucleus of the stria terminalis can also induce robust CTA. CGRP(PBN) neurons undergo plasticity following CTA, and inactivation of either Arc or Grin1 (genes involved in memory consolidation) prevents establishment of a strong CTA. Calcium imaging reveals that the novel food re-activates CGRP(PBN) neurons after conditioning. Inhibition of these neurons or inactivation of the Grin1 gene after conditioning attenuates CTA expression. Our results indicate that CGRP(PBN )neurons not only play a key role for learning food aversions but also contribute to the maintenance and expression of those memories.
引用
收藏
页码:891 / +
页数:14
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