Evidence map›Paper›PMID 35294287›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

Nociception and hypersensitivity involve distinct neurons and molecular transducers in

Pengyu Gu, Fei Wang, Ye Shang, Jingjing Liu, Jiaxin Gong, Wei Xie, Junhai Han, Yang Xiang

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

22 citing papers in PubMed, 26 citations in OpenAlex.

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  17. When Do We Start Caring About Insect Welfare?Neotropical entomology · 2023
    Review
  18. Review
  19. Nociception in fruit fly larvae.Frontiers in pain research (Lausanne, Switzerland) · 2023
    Review
  20. 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

8 authors at 2 institutions in 2 countries.

Pengyu GuDepartment of Neurobiology, University of Massachusetts Medical School, Worcester, MA 01605.ORCID 0000-0003-2571-3579
Fei WangDepartment of Neurobiology, University of Massachusetts Medical School, Worcester, MA 01605.
Ye ShangDepartment of Neurobiology, University of Massachusetts Medical School, Worcester, MA 01605.
Jingjing LiuSchool of Life Science and Technology, Key Laboratory of Developmental Genes and Human Disease, Southeast University, Nanjing 210096, China.
Jiaxin GongDepartment of Neurobiology, University of Massachusetts Medical School, Worcester, MA 01605.ORCID 0000-0001-5101-3109
Wei XieSchool of Life Science and Technology, Key Laboratory of Developmental Genes and Human Disease, Southeast University, Nanjing 210096, China.ORCID 0000-0002-9179-4787
Junhai HanSchool of Life Science and Technology, Key Laboratory of Developmental Genes and Human Disease, Southeast University, Nanjing 210096, China.ORCID 0000-0001-8941-2578
Yang XiangDepartment of Neurobiology, University of Massachusetts Medical School, Worcester, MA 01605.
University of Massachusetts Chan Medical School · USSoutheast University · CN

Funding

Molecular Mechanisms of nociceptor sensitizationR01NS089787 · NINDS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI XIANG, YANG · 2015 to 2019
$1.8M
Cellular and molecular mechanisms underlying neuronal activity-controlled regeneration specificityR21NS107924 · NINDS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI XIANG, YANG · 2018 to 2019
$481k
NINDS NIH HHS R01 NS089787NINDS NIH HHS R21 NS107924
6 · The paper itself

Abstract

Acute nociception is essential for survival by warning organisms against potential dangers, whereas tissue injury results in a nociceptive hypersensitivity state that is closely associated with debilitating disease conditions, such as chronic pain. Transient receptor potential (Trp) ion channels expressed in nociceptors detect noxious thermal and chemical stimuli to initiate acute nociception. The existing hypersensitivity model suggests that under tissue injury and inflammation, the same Trp channels in nociceptors are sensitized through transcriptional and posttranslational modulation, leading to nociceptive hypersensitivity. Unexpectedly and different from this model, we find that in Drosophila larvae, acute heat nociception and tissue injury-induced hypersensitivity involve distinct cellular and molecular mechanisms. Specifically, TrpA1-D in peripheral sensory neurons mediates acute heat nociception, whereas TrpA1-C in a cluster of larval brain neurons transduces the heat stimulus under the allodynia state. As a result, interfering with synaptic transmission of these brain neurons or genetic targeting of TrpA1-C blocks heat allodynia but not acute heat nociception. TrpA1-C and TrpA1-D are two splicing variants of TrpA1 channels and are coexpressed in these brain neurons. We further show that Gq-phospholipase C signaling, downstream of the proalgesic neuropeptide Tachykinin, differentially modulates these two TrpA1 isoforms in the brain neurons by selectively sensitizing heat responses of TrpA1-C but not TrpA1-D. Together, our studies provide evidence that nociception and noncaptive sensitization could be mediated by distinct sensory neurons and molecular sensors.

Indexed as

NociceptionTransient Receptor Potential ChannelsAnimalsDrosophilaNeuronsNociceptorsTransducersTransient Receptor Potential Channelsalternative splicingDrosophilanociceptionnociceptive hypersensitivitytransient receptor potential (Trp)

Identifiers

PMID35294287
PMCPMC8944580
OpenAlexW4220942538

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.