Evidence map›Paper›PMID 37694767›Full record

ArticleThe Journal of comparative neurology2023

Organization and morphology of calcitonin gene-related peptide-immunoreactive axons in the whole mouse stomach.

Jichao Ma, Duyen Nguyen, Jazune Madas, Ariege Bizanti, Anas Mistareehi, Andrew M Kwiat, Jin Chen, Mabelle Lin, Richard Christie, Peter Hunter and 6 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of comparative neurology, 2023. 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
0.9field-weighted citation impact, top 29% of its field
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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, 6 citations in OpenAlex.

  1. Article
  2. Gut-brain communication: types of sensory nerves and mechanisms of activation.Nature reviews. Gastroenterology & hepatology · 2026
    Review
  3. Review
  4. Review
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 5 institutions in 3 countries.

Jichao Ma *Burnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, Florida, USA.
Duyen Nguyen *Burnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, Florida, USA.ORCID 0000-0002-2093-2396
Jazune MadasBurnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, Florida, USA.
Ariege BizantiBurnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, Florida, USA.ORCID 0000-0002-8025-0135
Anas MistareehiBurnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, Florida, USA.
Andrew M KwiatBurnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, Florida, USA.
Jin ChenBurnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, Florida, USA.ORCID 0000-0001-7617-1664
Mabelle LinAuckland Bioengineering Institute, University of Auckland, Auckland, New Zealand.ORCID 0000-0002-6388-2181
Richard ChristieAuckland Bioengineering Institute, University of Auckland, Auckland, New Zealand.ORCID 0000-0003-4336-4640
Peter HunterAuckland Bioengineering Institute, University of Auckland, Auckland, New Zealand.ORCID 0000-0001-9665-4145
Maci HealMBF Bioscience, Williston, Vermont, USA.ORCID 0000-0001-5097-1030
Shane BaldwinMBF Bioscience, Williston, Vermont, USA.
Susan TappanRock Maple Science, Hinesburg, Vermont, USA.ORCID 0000-0001-5120-3770
John B FurnessDepartment of Anatomy & Physiology, Florey Institute of Neuroscience and Mental Health, University of Melbourne, Parkville, Victoria, Australia.ORCID 0000-0002-0219-3438
Terry L PowleyDepartment of Psychological Sciences, Purdue University, West Lafayette, Indiana, USA.ORCID 0000-0001-6689-7058
Zixi Jack ChengBurnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, Florida, USA.ORCID 0000-0002-7941-8527
University of Central Florida · USUniversity of Auckland · NZMBF Bioscience (United States) · USPurdue University West Lafayette · USThe University of Melbourne · AU

Funding

Multi-scale, multi-organ, multi-species SPARC map managementOT3OD025349 · OD · UNIVERSITY OF AUCKLAND · PI HUNTER, PETER JOHN, NICKERSON, DAVID PHILLIP · 2017 to 2024
$16.3M
Nociceptive Afferent Topographical Innervation of the Heart and StomachU01NS113867 · NINDS · UNIVERSITY OF CENTRAL FLORIDA · PI CHENG, ZIXI JACK · 2019 to 2021
$1.6M
Chronic Intermittent Hypoxia: Sympathetic and Intrinsic Cardiac GanglionicInnervationR15HL137143 · NHLBI · UNIVERSITY OF CENTRAL FLORIDA · PI CHENG, ZIXI JACK · 2018 to 2018
$431k
NHLBI NIH HHS R15 HL137143NIH HHS NIHR15HL137143-01A1NIH HHS NIHU01NS113867-01NIH HHS OT3 OD025349NINDS NIH HHS U01 NS113867
6 · The paper itself

Abstract

Nociceptive afferent axons innervate the stomach and send signals to the brain and spinal cord. Peripheral nociceptive afferents can be detected with a variety of markers (e.g., substance P [SP] and calcitonin gene-related peptide [CGRP]). We recently examined the topographical organization and morphology of SP-immunoreactive (SP-IR) axons in the whole mouse stomach muscular layer. However, the distribution and morphological structure of CGRP-IR axons remain unclear. We used immunohistochemistry labeling and applied a combination of imaging techniques, including confocal and Zeiss Imager M2 microscopy, Neurolucida 360 tracing, and integration of axon tracing data into a 3D stomach scaffold to characterize CGRP-IR axons and terminals in the whole mouse stomach muscular layers. We found that: (1) CGRP-IR axons formed extensive terminal networks in both ventral and dorsal stomachs. (2) CGRP-IR axons densely innervated the blood vessels. (3) CGRP-IR axons ran in parallel with the longitudinal and circular muscles. Some axons ran at angles through the muscular layers. (4) They also formed varicose terminal contacts with individual myenteric ganglion neurons. (5) CGRP-IR occurred in DiI-labeled gastric-projecting neurons in the dorsal root and vagal nodose ganglia, indicating CGRP-IR axons were visceral afferent axons. (6) CGRP-IR axons did not colocalize with tyrosine hydroxylase or vesicular acetylcholine transporter axons in the stomach, indicating CGRP-IR axons were not visceral efferent axons. (7) CGRP-IR axons were traced and integrated into a 3D stomach scaffold. For the first time, we provided a topographical distribution map of CGRP-IR axon innervation of the whole stomach muscular layers at the cellular/axonal/varicosity scale.

Indexed as

Calcitonin Gene-Related PeptideStomachAnimalsAxonsMiceNerve FibersNeuronsCalcitonin Gene-Related PeptideCGRPdorsal root ganglialongitudinal and circular musclesmyenteric plexusnociceptive afferentstomachvagal nodose ganglia

Identifiers

PMID37694767
PMCPMC10593087
OpenAlexW4386593029

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.