Evidence map›Paper›PMID 42046407›Full record

ArticleCNS neuroscience & therapeutics2026

Whole-Brain Neural Connectivity to Cholinergic Neurons in the Lower Thoracic Intermediolateral Column.

Yuan-Jun Yang, Kai-Ying Zhang, Bin-Bin Li, Xia-Wan Liu, Jing-Rong Li, Yi-Nuo Liu, Yu-Han Liu, Ji Li, Xiang-Shan Yuan, Ming Zhong

Abstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Yuan-Jun YangDepartment of Critical Care Medicine, Zhongshan Hospital, Fudan University, Shanghai, China.
Kai-Ying ZhangDepartment of Anatomy and Histoembryology, School of Basic Medical Sciences, Fudan University, Shanghai, China.
Bin-Bin LiDepartment of Critical Care Medicine, Zhongshan Hospital, Fudan University, Shanghai, China.
Xia-Wan LiuDepartment of Anatomy and Histoembryology, School of Basic Medical Sciences, Fudan University, Shanghai, China.
Jing-Rong LiDepartment of Anatomy and Histoembryology, School of Basic Medical Sciences, Fudan University, Shanghai, China.
Yi-Nuo LiuDepartment of Anatomy and Histoembryology, School of Basic Medical Sciences, Fudan University, Shanghai, China.
Yu-Han LiuDepartment of Anatomy and Histoembryology, School of Basic Medical Sciences, Fudan University, Shanghai, China.
Ji LiDepartment of Pancreatic Surgery, Huashan Hospital, Fudan University, Shanghai, China.
Xiang-Shan YuanDepartment of Anatomy and Histoembryology, School of Basic Medical Sciences, Fudan University, Shanghai, China.ORCID https://orcid.org/0000-0003-2365-8756
Ming ZhongDepartment of Critical Care Medicine, Zhongshan Hospital, Fudan University, Shanghai, China.ORCID https://orcid.org/0000-0002-5578-5277

Funding

Key Disciplines of the Three-year Action Plan for Strengthening the Construction of Public Health System in Shanghai GWVI-11.1-14National Natural Science Foundation of China 32171142National Natural Science Foundation of China 32371192Open Project of Key Laboratory of Longevity and Aging-related Diseases (Guangxi Medical University), Ministry of Education KLLAD202501Open Project of State Key Laboratory of Respiratory Disease SKLRD-ОР-202321Shanghai Key Laboratory of Lung Inflammation and Injury
6 · The paper itself

Abstract

objectiveThe intermediolateral column (IML) serves as a crucial hub for sympathetic information processing between the brain and peripheral organs, with its defining hallmark being the presence of cholinergic neurons expressing choline acetyltransferase (ChAT). Specifically, the IML of the lower thoracic cord plays a pivotal role in regulating abdominal metabolic and digestive viscera. However, little is known about the whole-brain neural connectivity targeting these lower thoracic IML cholinergic neurons, necessitating further investigation.

methodsSpecific retrograde tracing virus was injected into the lower thoracic IML of ChAT-Cre transgenic mice expressing Cre in the cholinergic neurons. After the virus has fully expressed, brain and spinal cord sections were prepared for whole-brain fluorescence imaging and quantitative analysis.

resultsWe found that virally labeled neurons were detected in 40 brain regions of ChAT-Cre mice, encompassing the telencephalon, diencephalon, and brainstem. Afferents were predominantly concentrated in 25 brainstem regions, with the pons providing the highest total number of afferents and the medulla offering the highest afferent density across both hemispheres. Although a small subset of regions exhibited strictly unilateral inputs or hemispheric preference, the overall projection pattern remained bilateral. Furthermore, our results revealed extensive projections to the IML from regions classically implicated in sympathetic outflow regulation and homeostatic control, including the paraventricular hypothalamic nucleus (PVN), lateral hypothalamic area (LH), and rostroventrolateral reticular nucleus (RVLM). In addition, inputs were also observed from motor-related regions, such as primary and secondary motor cortices (M1, M2), red nucleus (RN), and gigantocellular reticular nucleus (Gi), suggesting a potential anatomical basis for the central coupling of somatic motor and sympathetic functions.

conclusionOur study provides a comprehensive whole-brain anatomical map of inputs to lower thoracic IML cholinergic neurons. This extensive supraspinal network, integrating classical sympathetic and homeostatic centers with motor-related regions, suggests a potential anatomical basis for the central coordination of somatic motor and autonomic functions.

Indexed as

BrainCholinergic NeuronsSpinal CordAnimalsCholine O-AcetyltransferaseMaleMiceMice, TransgenicNeural PathwaysCholine O-Acetyltransferasecholinergic neuronsrabies virusspinal cordsympathetic nervous system

Identifiers

PMID42046407
PMCPMC13121841

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.