Evidence map›Paper›PMID 21383614›Full record

ArticleAnesthesiology2011

Disruption of the transient receptor potential vanilloid 1 can affect survival, bacterial clearance, and cytokine gene expression during murine sepsis.

Virginia Guptill, Xizhong Cui, Alfia Khaibullina, Jason M Keller, Nicholas Spornick, Andrew Mannes, Michael Iadarola, Zenaide M N Quezado

Open access · bronzeAbstract read
In one paragraph

Article in Anesthesiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.1field-weighted citation impact, top 27% 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

26 citing papers in PubMed, 44 citations in OpenAlex.

  1. TRPV1: The key bridge in neuroimmune interactions.Journal of intensive medicine · 2024
    Review
  2. Article
  3. Review
  4. Role of Kynurenine and Its Derivatives in the Neuroimmune System.International journal of molecular sciences · 2024
    Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. The Effect of Anesthesia on the Immune System in Colorectal Cancer Patients.Canadian journal of gastroenterology & hepatology · 2018
    Review
  15. Journal of immunology (Baltimore, Md. : 1950) · 2017
    Article
  16. Extraoral Taste Receptor Discovery: New Light on Ayurvedic Pharmacology.Evidence-based complementary and alternative medicine : eCAM · 2017
    Review
  17. Review
  18. Review
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  20. Article
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 1 institution in 1 country.

Virginia GuptillDepartment of Perioperative Medicine, National Institutes of Health Clinical Center, Bethesda, Maryland, USA.
Xizhong Cui
Alfia Khaibullina
Jason M Keller
Nicholas Spornick
Andrew Mannes
Michael Iadarola
Zenaide M N Quezado
Company of Biologists · GB

Funding

Integrative And Molecular Studies Of Pain And Pain ControlZIADE000688 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI IADAROLA, MICHAEL J. · 2009 to 2012
$4.0M
The role of neuronal nitric oxide on pain thresholdsZ01CL008078 · CLC · CLINICAL CENTER · PI QUEZADO, ZENAIDE · 2005 to 2008
$273k
The role of neuronal nitric oxide synthase in a model of peritonitis and sepsisZIACL008047 · CLC · CLINICAL CENTER · PI HENDERSON, DAVID C · 2009 to 2012
$0k
The role of neuronal nitric oxide on current vocalization thresholdsZIACL008078 · CLC · CLINICAL CENTER · PI HENDERSON, DAVID C · 2009 to 2012
$0k
Intramural NIH HHS Z01 CL008078
6 · The paper itself

Abstract

backgroundPrevious studies suggest that the transient receptor potential vanilloid 1 (TRPV1) channel has a role in sepsis, but it is unclear whether its effect on survival and immune response is beneficial or harmful.

methodsWe studied the effects of genetic (Trpv1-knockout vs. wild-type [WT] mice) and pharmacologic disruption of TRPV1 with resiniferatoxin (an agonist) or capsazepine (an antagonist) on mortality, bacterial clearance, and cytokine expression during lipopolysaccharide or cecal ligation and puncture-induced sepsis.

resultsAfter cecal ligation and puncture, genetic disruption of TRPV1 in Trpv1-knockout versus WT mice was associated with increased mortality risk (hazard ratio, 2.17; 95% CI, 1.23-3.81; P = 0.01). Furthermore, pharmacologic disruption of TRPV1 with intrathecal resiniferatoxin, compared with vehicle, increased mortality risk (hazard ratio, 1.80; 95% CI, 1.05-3.2; P = 0.03) in WT, but not in Trpv1-knockout, mice. After lipopolysaccharide, neither genetic (Trpv1 knockout) nor pharmacologic disruption of TRPV1 with resiniferatoxin had significant effect on survival compared with respective controls. In contrast, after lipopolysaccharide, pharmacologic disruption of TRPV1 with capsazepine, compared with vehicle, increased mortality risk (hazard ratio, 1.92; 95% CI, 1.02-3.61; P = 0.04) in WT animals. Furthermore, after cecal ligation and puncture, increased mortality in resiniferatoxin-treated WT animals was associated with higher blood bacterial count (P = 0.0004) and higher nitrate/nitrite concentrations and down-regulation of tumor necrosis factor α expression (P = 0.004) compared with controls.

conclusionsGenetic or pharmacologic disruption of TRPV1 can affect mortality, blood bacteria clearance, and cytokine response in sepsis in patterns that may vary according to the sepsis-inducing event and the method of TRPV1 disruption.

Indexed as

AnimalsBacterial LoadCapsaicinCecumCytokinesDisease Models, AnimalDiterpenesDown-RegulationFemaleFlow CytometryGene ExpressionLigationLipopolysaccharidesMiceMice, Inbred C57BLMice, KnockoutCapsaicincapsazepineCytokinesDiterpenesLipopolysaccharidesresiniferatoxinTRPV1 protein, mouseTRPV Cation ChannelsTumor Necrosis Factor-alpha

Identifiers

PMID21383614
PMCPMC3119195
OpenAlexW2058595533

What OpenQuestion holds

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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.