Evidence map›Paper›PMID 39953101›Full record

ArticleScientific reports2025

The neuronal and glial cell diversity in the celiac ganglion revealed by single-nucleus RNA sequencing.

Hirosato Kanda, Hiroki Yamanaka, Yi Dai, Koichi Noguchi

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Hirosato KandaLaboratory of Anatomy, School of Pharmacy, Hyogo Medical University, Kobe, Hyogo, 650-8530, Japan. kanda@hyo-med.ac.jp.
Hiroki YamanakaLaboratory of Anatomy, School of Pharmacy, Hyogo Medical University, Kobe, Hyogo, 650-8530, Japan.
Yi DaiLaboratory of Basic Pain Research, Hyogo Medical University, Kobe, Hyogo, 650-8530, Japan.
Koichi NoguchiLaboratory of Basic Pain Research, Hyogo Medical University, Kobe, Hyogo, 650-8530, Japan.

Funding

Japan Society for the Promotion of Science 22K06489
6 · The paper itself

Abstract

The sympathetic nervous system regulates various visceral functions, including those of the heart, lungs, and digestive system, and maintains homeostasis. The prevertebral ganglia (PVG) in the peripheral nervous system serve as a vital relay station, transmitting efferent signals to visceral organs. The PVG receives innervation from intestinofugal afferent neurones (IFANs) that originate from the enteric plexus, as well as from spinal sensory nerves that innervate the enteric tract. While neural circuits comprising sensory and sympathetic nerves have been proposed, the exact diversity of the individual neurones in these circuits is still not well characterized in rats. In this study, we employed single-nuclei RNA-sequencing to characterize all the cell types present in the celiac ganglion (CG). We identified five distinct neural clusters, including celiac noradrenergic and celiac cholinergic neurones (CNA1-4, CACh). Among these, the CNA3 cluster expressed Tacr1 and Cckar, while the CACh cluster expressed Ramp1. Furthermore, we characterised Mki67-positive proliferating cells and found that they expressed genes associated with satellite glial cells (SGCs). Additionally, general resident and sympathetic SGCs with distinct SGC clusters were localised within the CG. Our data provide a valuable resource for investigating neural circuits within the PVG and for identifying target organs innervated by specific neuronal populations.

Indexed as

Ganglia, SympatheticNeurogliaNeuronsAnimalsMaleRatsSequence Analysis, RNACeliac ganglionSingle-nuclei RNA-sequencingSympathetic nervous system

Identifiers

PMID39953101
PMCPMC11828872

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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.