Evidence map›Paper›PMID 18376408›Full record

ArticleNature medicine2008

Neurotensin increases mortality and mast cells reduce neurotensin levels in a mouse model of sepsis.

Adrian M Piliponsky, Ching-Cheng Chen, Toshihiko Nishimura, Martin Metz, Eon J Rios, Paul R Dobner, Etsuko Wada, Keiji Wada, Sherma Zacharias, Uma M Mohanasundaram and 6 more

Open access · greenAbstract read
In one paragraph

Article in Nature medicine, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

64 citing papers in PubMed, 127 citations in OpenAlex.

  1. Article
  2. IL-18-associated basophil and mast cell activation in sepsis.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Mast Cell and Basophil Granule Proteases -Frontiers in immunology · 2022
    Review
  12. Studying Kidney Diseases Using Organoid Models.Frontiers in cell and developmental biology · 2022
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Absence of neurotensin attenuates intestinal dysbiosis and inflammation by maintaining Mmp7/α-defensin axis in diet-induced obese mice.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    Article
  18. Article
  19. Article
  20. Review

4 more citing papers are in PubMed but not listed here.

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

16 authors at 8 institutions in 4 countries.

Adrian M PiliponskyDepartment of Pathology, Stanford University School of Medicine, Stanford, California 94305, USA.
Ching-Cheng Chen
Toshihiko Nishimura
Martin Metz
Eon J Rios
Paul R Dobner
Etsuko Wada
Keiji Wada
Sherma Zacharias
Uma M Mohanasundaram
James D Faix
Magnus Abrink
Gunnar Pejler
Ronald G Pearl
Mindy Tsai
Stephen J Galli
Stanford University · USJapan Science and Technology Agency · JPNational Center of Neurology and Psychiatry · JPStanford Medicine · USSwedish University of Agricultural Sciences · SEUniversity of Applied Sciences Mainz · DEUniversity of Massachusetts Chan Medical School · USUppsala University · SE

Funding

Role of Mast Cells in Inflammation and ImmunityR01CA072074 · NCI · STANFORD UNIVERSITY · PI GALLI, STEPHEN JOSEPH · 1996 to 2010
$4.4M
Expression and Modulation of Mast Cell Function in AsthmaR01AI070813 · NIAID · STANFORD UNIVERSITY · PI GALLI, STEPHEN JOSEPH · 2006 to 2010
$2.5M
Regulation of Mast Cell Development and FunctionR01AI023990 · NIAID · STANFORD UNIVERSITY · PI GALLI, STEPHEN JOSEPH · 1986 to 2010
$2.4M
Paired lg-Like Receptor as a Regulator of Hematopoietic Stem Cell FunctionR00HL087936 · NHLBI · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI CHEN, CHING-CHENG · 2010 to 2012
$747k
Paired lg-Like Receptor as a Regulator of Hematopoietic Stem Cell FunctionK99HL087936 · NHLBI · STANFORD UNIVERSITY · PI CHEN, CHING-CHENG · 2007 to 2008
$172k
NCI NIH HHS R01 CA072074NHLBI NIH HHS K99 HL087936NHLBI NIH HHS R00 HL087936NIAID NIH HHS R01 AI023990NIAID NIH HHS R01 AI070813
6 · The paper itself

Abstract

Sepsis is a complex, incompletely understood and often fatal disorder, typically accompanied by hypotension, that is considered to represent a dysregulated host response to infection. Neurotensin (NT) is a 13-amino-acid peptide that, among its multiple effects, induces hypotension. We find that intraperitoneal and plasma concentrations of NT are increased in mice after severe cecal ligation and puncture (CLP), a model of sepsis, and that mice treated with a pharmacological antagonist of NT, or NT-deficient mice, show reduced mortality during severe CLP. In mice, mast cells can degrade NT and reduce NT-induced hypotension and CLP-associated mortality, and optimal expression of these effects requires mast cell expression of neurotensin receptor 1 and neurolysin. These findings show that NT contributes to sepsis-related mortality in mice during severe CLP and that mast cells can lower NT concentrations, and suggest that mast cell-dependent reduction in NT levels contributes to the ability of mast cells to enhance survival after CLP.

Indexed as

AnimalsCell DegranulationDisease Models, AnimalFemaleHumansHypotensionMaleMast CellsMetalloendopeptidasesMiceMice, CongenicMice, Inbred C57BLMice, KnockoutMice, Mutant StrainsNeurotensinProto-Oncogene Proteins c-kitMetalloendopeptidasesneurolysinNeurotensinneurotensin type 1 receptorProto-Oncogene Proteins c-kitReceptors, Neurotensin

Identifiers

PMID18376408
PMCPMC2873870
OpenAlexW2095142211

What OpenQuestion holds

Textmetadata
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.