Viscerosensory signalling to the nucleus accumbens via the solitary tract nucleus

Author:

McDougall Stuart J.12ORCID,Ong Zhi Yi3ORCID,Heller Rosa1,Horton Anna1ORCID,Thek Kimberly K.1ORCID,Choi Eun A.3,McNally Gavan P.3ORCID,Lawrence Andrew J.12ORCID

Affiliation:

1. Florey Institute of Neuroscience and Mental Health Parkville Victoria Australia

2. Florey Department of Neuroscience and Mental Health University of Melbourne Parkville Victoria Australia

3. School of Psychology UNSW Sydney Kensington New South Wales Australia

Abstract

AbstractThe nucleus of the solitary tract (NTS) receives direct viscerosensory vagal afferent input that drives autonomic reflexes, neuroendocrine function and modulates behaviour. A subpopulation of NTS neurons project to the nucleus accumbens (NAc); however, the function of this NTS‐NAc pathway remains unknown. A combination of neuroanatomical tracing, slice electrophysiology and fibre photometry was used in mice and/or rats to determine how NTS‐NAc neurons fit within the viscerosensory network. NTS‐NAc projection neurons are predominantly located in the medial and caudal portions of the NTS with 54 ± 7% (mice) and 65 ± 3% (rat) being TH‐positive, representing the A2 NTS cell group. In horizontal brainstem slices, solitary tract (ST) stimulation evoked excitatory post‐synaptic currents (EPSCs) in NTS‐NAc projection neurons. The majority (75%) received low‐jitter, zero‐failure EPSCs characteristic of monosynaptic ST afferent input that identifies them as second order to primary sensory neurons. We then examined whether NTS‐NAc neurons respond to cholecystokinin (CCK, 20 μg/kg ip) in vivo in both mice and rats. Surprisingly, there was no difference in the number of activated NTS‐NAc cells between CCK and saline‐treated mice. In rats, just 6% of NTS‐NAc cells were recruited by CCK. As NTS TH neurons are the primary source for NAc noradrenaline, we measured noradrenaline release in the NAc and showed that NAc noradrenaline levels declined in response to cue‐induced reward retrieval but not foot shock. Combined, these findings suggest that high‐fidelity afferent information from viscerosensory afferents reaches the NAc. These signals are likely unrelated to CCK‐sensitive vagal afferents but could interact with other sensory and higher order inputs to modulate learned appetitive behaviours.image

Funder

Australian Research Council

National Health and Medical Research Council

Publisher

Wiley

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3