Evidence map›Paper›PMID 31969645›Full record

ArticleScientific reports2020

Behavioral characterization of a CRISPR-generated TRPA1 knockout rat in models of pain, itch, and asthma.

Rebecca M Reese, Michelle Dourado, Keith Anderson, Søren Warming, Kimberly L Stark, Alessia Balestrini, Eric Suto, Wyne Lee, Lorena Riol-Blanco, Shannon D Shields and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.2field-weighted citation impact, top 6% 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

29 citing papers in PubMed, 55 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. TRP Ion Channels in Immune Cells and Their Implications for Inflammation.International journal of molecular sciences · 2024
    Review
  5. Review
  6. Article
  7. Review
  8. Cannabis Pharmacogenomics: A Path to Personalized Medicine.Current issues in molecular biology · 2023
    Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. TRPA1 Role in Inflammatory Disorders: What Is Known So Far?International journal of molecular sciences · 2022
    Review
  14. Recent Advances in the Production of Genome-Edited Rats.International journal of molecular sciences · 2022
    Review
  15. Role of TRP ion channels in pruritus.Neuroscience letters · 2022
    Review
  16. Article
  17. Article
  18. Article
  19. 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

11 authors at 1 institution in 1 country.

Rebecca M Reese *Department of Neuroscience, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Michelle Dourado *Department of Neuroscience, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Keith AndersonDepartment of Molecular Biology, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.ORCID http://orcid.org/0000-0001-8713-4965
Søren WarmingDepartment of Molecular Biology, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.ORCID http://orcid.org/0000-0002-5721-0741
Kimberly L StarkDepartment of Neuroscience, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Alessia BalestriniDepartment of Immunology, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Eric SutoDepartment of Immunology, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Wyne LeeDepartment of Immunology, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Lorena Riol-BlancoDepartment of Immunology, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
Shannon D ShieldsDepartment of Neuroscience, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA.
David H HackosDepartment of Neuroscience, Genentech, 1 DNA Way, South San Francisco, CA, 94080, USA. hackos.david@gene.com.
Gene Therapy Laboratory · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The transient receptor potential (TRP) superfamily of ion channels has garnered significant attention by the pharmaceutical industry. In particular, TRP channels showing high levels of expression in sensory neurons such as TRPV1, TRPA1, and TRPM8, have been considered as targets for indications where sensory neurons play a fundamental role, such as pain, itch, and asthma. Modeling these indications in rodents is challenging, especially in mice. The rat is the preferred species for pharmacological studies in pain, itch, and asthma, but until recently, genetic manipulation of the rat has been technically challenging. Here, using CRISPR technology, we have generated a TRPA1 KO rat to enable more sophisticated modeling of pain, itch, and asthma. We present a detailed phenotyping of the TRPA1 KO rat in models of pain, itch, and asthma that have previously only been investigated in the mouse. With the exception of nociception induced by direct TRPA1 activation, we have found that the TRPA1 KO rat shows apparently normal behavioral responses in multiple models of pain and itch. Immune cell infiltration into the lung in the rat OVA model of asthma, on the other hand, appears to be dependent on TRPA1, similar to was has been observed in TRPA1 KO mice. Our hope is that the TRPA1 KO rat will become a useful tool in further studies of TRPA1 as a drug target.

Indexed as

AnimalsAsthmaBehavior, AnimalClustered Regularly Interspaced Short Palindromic RepeatsPainPhenotypePruritusRatsRats, TransgenicTRPA1 Cation ChannelTRPA1 Cation Channel

Identifiers

PMID31969645
PMCPMC6976688
OpenAlexW3001350449

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.