Evidence map›Paper›PMID 35534865›Full record

ArticleMolecular brain2022

Exogenous expression of an allatotropin-related peptide receptor increased the membrane excitability in Aplysia neurons.

Guo Zhang, Shi-Qi Guo, Si-Yuan Yin, Wang-Ding Yuan, Ping Chen, Ji-Il Kim, Hui-Ying Wang, Hai-Bo Zhou, Abraham J Susswein, Bong-Kiun Kaang and 1 more

Open access · goldAbstract read
In one paragraph

Article in Molecular brain, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 40% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
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  4. Characterization of anFrontiers in pharmacology · 2023
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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

11 authors at 4 institutions in 4 countries.

Guo Zhang *State Key Laboratory of Pharmaceutical Biotechnology, Institute for Brain Sciences, Advanced Institute for Life Sciences, School of Life Sciences, Nanjing University, Nanjing, 210023, Jiangsu, China.
Shi-Qi Guo *State Key Laboratory of Pharmaceutical Biotechnology, Institute for Brain Sciences, Advanced Institute for Life Sciences, School of Life Sciences, Nanjing University, Nanjing, 210023, Jiangsu, China.
Si-Yuan Yin *State Key Laboratory of Pharmaceutical Biotechnology, Institute for Brain Sciences, Advanced Institute for Life Sciences, School of Life Sciences, Nanjing University, Nanjing, 210023, Jiangsu, China.
Wang-Ding Yuan *State Key Laboratory of Pharmaceutical Biotechnology, Institute for Brain Sciences, Advanced Institute for Life Sciences, School of Life Sciences, Nanjing University, Nanjing, 210023, Jiangsu, China.
Ping ChenState Key Laboratory of Pharmaceutical Biotechnology, Institute for Brain Sciences, Advanced Institute for Life Sciences, School of Life Sciences, Nanjing University, Nanjing, 210023, Jiangsu, China.
Ji-Il KimSchool of Biological Sciences, Seoul National University, 1, Gwanak-ro, Gwanak-gu, Seoul, 08826, Korea.
Hui-Ying WangState Key Laboratory of Pharmaceutical Biotechnology, Institute for Brain Sciences, Advanced Institute for Life Sciences, School of Life Sciences, Nanjing University, Nanjing, 210023, Jiangsu, China.
Hai-Bo ZhouSchool of Electronic Science and Engineering, Nanjing University, Nanjing, 210023, Jiangsu, China.
Abraham J SussweinThe Mina and Everard Goodman Faculty of Life Sciences, Bar Ilan University, 52900, Ramat Gan, Israel.
Bong-Kiun KaangSchool of Biological Sciences, Seoul National University, 1, Gwanak-ro, Gwanak-gu, Seoul, 08826, Korea.
Jian JingState Key Laboratory of Pharmaceutical Biotechnology, Institute for Brain Sciences, Advanced Institute for Life Sciences, School of Life Sciences, Nanjing University, Nanjing, 210023, Jiangsu, China. jingj01@live.com.ORCID 0000-0003-1422-143X
State Key Laboratory of Pharmaceutical BiotechnologyPeng Cheng Laboratory · CNSeoul National University · KRBar-Ilan University · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neuropeptides act mostly on a class of G-protein coupled receptors, and play a fundamental role in the functions of neural circuits underlying behaviors. However, physiological functions of some neuropeptide receptors are poorly understood. Here, we used the molluscan model system Aplysia and microinjected the exogenous neuropeptide receptor apATRPR (Aplysia allatotropin-related peptide receptor) with an expression vector (pNEX3) into Aplysia neurons that did not express the receptor endogenously. Physiological experiments demonstrated that apATRPR could mediate the excitability increase induced by its ligand, apATRP (Aplysia allatotropin-related peptide), in the Aplysia neurons that now express the receptor. This study provides a definitive evidence for a physiological function of a neuropeptide receptor in molluscan animals.

Indexed as

AplysiaNeuropeptidesAnimalsInsect HormonesNeuronsReceptors, NeuropeptideallatotropinInsect HormonesNeuropeptidesReceptors, NeuropeptideAplysiaElectrophysiologyG-protein coupled receptorsNeuronal excitabilityNeuropeptidePlasmid microinjection

Identifiers

PMID35534865
PMCPMC9082908
OpenAlexW4229372988

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.