Evidence map›Paper›PMID 34472489›Full record

ArticleNeural regeneration research2022

Involvement of A5/A7 noradrenergic neurons and B2 serotonergic neurons in nociceptive processing: a fiber photometry study.

Shunpei Moriya, Akira Yamashita, Daiki Masukawa, Junichi Sakaguchi, Yoko Ikoma, Yoshimune Sameshima, Yuki Kambe, Akihiro Yamanaka, Tomoyuki Kuwaki

Open access · goldAbstract read
In one paragraph

Article in Neural regeneration research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Review
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

9 authors at 3 institutions in 1 country.

Shunpei MoriyaDepartment of Physiology, Kagoshima University Graduate School of Medical and Dental Science, Kagoshima, Japan.
Akira YamashitaDepartment of Physiology, Kagoshima University Graduate School of Medical and Dental Science, Kagoshima, Japan.
Daiki MasukawaDepartment of Molecular Pharmacology and Neurobiology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Junichi SakaguchiDepartment of Physiology, Kagoshima University Graduate School of Medical and Dental Science, Kagoshima, Japan.
Yoko IkomaDepartment of Physiology, Kagoshima University Graduate School of Medical and Dental Science, Kagoshima, Japan.
Yoshimune SameshimaDepartment of Pharmacology, Kagoshima University Graduate School of Medical and Dental Science, Kagoshima, Japan.
Yuki KambeDepartment of Pharmacology, Kagoshima University Graduate School of Medical and Dental Science, Kagoshima, Japan.
Akihiro YamanakaResearch Institute of Environmental Medicine, Nagoya University, Nagoya, Japan.
Tomoyuki KuwakiDepartment of Physiology, Kagoshima University Graduate School of Medical and Dental Science, Kagoshima, Japan.
Kagoshima University · JPNagoya University · JPYokohama City University · JP

Funding

Quédate Tranquila: A Mobile, Web-based Stress Management Intervention for Hispanic WomenR44MD017105 · NIMHD · ISA ASSOCIATES, INC. · PI RIOS, DEBRA · 2024 to 2025
$1.6M
Quédate Tranquila: A Mobile, Web-based Stress Management Intervention for Hispanic WomenR43MD017105 · NIMHD · ISA ASSOCIATES, INC. · PI RIOS, DEBRA · 2021 to 2021
$256k
NIMHD NIH HHS R43 MD017105NIMHD NIH HHS R44 MD017105
6 · The paper itself

Abstract

In the central nervous system, the A6 noradrenaline (NA) and the B3 serotonin (5-HT) cell groups are well-recognized players in the descending antinociceptive system, while other NA/5-HT cell groups are not well characterized. A5/A7 NA and B2 5-HT cells project to the spinal horn and form descending pathways. We recorded G-CaMP6 green fluorescence signal intensities in the A5/A7 NA and the B2 5-HT cell groups of awake mice in response to acute tail pinch stimuli, acute heat stimuli, and in the context of a non-noxious control test, using fiber photometry with a calcium imaging system. We first introduced G-CaMP6 in the A5/A7 NA or B2 5-HT neuronal soma, using transgenic mice carrying the tetracycline-controlled transactivator transgene under the control of either a dopamine β-hydroxylase or a tryptophan hydroxylase-2 promoters and by the site-specific injection of adeno-associated virus (AAV-TetO(3G)-G-CaMP6). After confirming the specific expression patterns of G-CaMP6, we recorded G-CaMP6 green fluorescence signals in these sites in awake mice in response to acute nociceptive stimuli. G-CaMP6 fluorescence intensity in the A5, A7, and B2 cell groups was rapidly increased in response to acute nociceptive stimuli and soon after, it returned to baseline fluorescence intensity. This was not observed in the non-noxious control test. The results indicate that acute nociceptive stimuli rapidly increase the activities of A5/A7 NA or B2 5-HT neurons but the non-noxious stimuli do not. The present study suggests that A5/A7 NA or B2 5-HT neurons play important roles in nociceptive processing in the central nervous system. We suggest that A5/A7/B2 neurons may be new therapeutic targets. All performed procedures were approved by the Institutional Animal Use Committee of Kagoshima University (MD17105) on February 22, 2018.

Indexed as

A5 NA neuronsA7 NA neuronsB2 5-HT neuronsDBH-tTA micefiber photometryG-CaMP6mCherrymonoaminergic signalingnociceptionTPH-tTA mice

Identifiers

PMID34472489
PMCPMC8530127
OpenAlexW3121857659

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.