Evidence map›Paper›PMID 30806746›Full record

ArticlePsychopharmacology2019

Lipocalin-2 is dispensable in inflammation-induced sickness and depression-like behavior.

Elisabeth G Vichaya, Phillip S Gross, Darlene J Estrada, Steve W Cole, Aaron J Grossberg, Scott E Evans, Michael J Tuvim, Burton F Dickey, Robert Dantzer

Open access · greenAbstract read
In one paragraph

Article in Psychopharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.0field-weighted citation impact, top 29% 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

17 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Potential Role of Bmal1 in Lipopolysaccharide-Induced Depression-Like Behavior and its Associated "Inflammatory Storm".Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Lipocalin-2 and Cerebral Stroke.Frontiers in molecular neuroscience · 2022
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. 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

9 authors at 3 institutions in 1 country.

Elisabeth G VichayaDepartment of Symptom Research, Division of Internal Medicine, University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Unit 384, Houston, TX, 77030, USA. egvichaya@mdanderson.org.ORCID http://orcid.org/0000-0001-9421-7419
Phillip S GrossDepartment of Symptom Research, Division of Internal Medicine, University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Unit 384, Houston, TX, 77030, USA.
Darlene J EstradaDepartment of Symptom Research, Division of Internal Medicine, University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Unit 384, Houston, TX, 77030, USA.
Steve W ColeDepartments of Medicine and Psychiatry & Biobehavioral Sciences, Jonsson Comprehensive Cancer Center and Norman Cousins Center, UCLA School of Medicine, Los Angeles, CA, USA.
Aaron J GrossbergDepartment of Radiation Medicine, School of Medicine, Oregon Health & Sciences University, Portland, OR, USA.
Scott E EvansDepartment of Pulmonary Medicine, Division of Internal Medicine, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Michael J TuvimDepartment of Pulmonary Medicine, Division of Internal Medicine, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Burton F DickeyDepartment of Pulmonary Medicine, Division of Internal Medicine, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Robert DantzerDepartment of Symptom Research, Division of Internal Medicine, University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Unit 384, Houston, TX, 77030, USA.
The University of Texas MD Anderson Cancer Center · USOregon Health & Science University · USUCLA Jonsson Comprehensive Cancer Center

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Neuroimmune Mechanisms of Recovery from Comorbid Depression and Chronic PainR01NS073939 · NINDS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DANTZER, ROBERT, HEIJNEN, COBI J · 2011 to 2020
$4.0M
The Metabolic Basis of Cancer-Related FatigueR01CA193522 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DANTZER, ROBERT · 2015 to 2023
$3.8M
Controlling the core airway mucin secretion machinery to prevent pathophysiologyR01HL129795 · NHLBI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DICKEY, BURTON F · 2015 to 2023
$3.8M
Blood-Brain Barrier Transport Mechanisms in Inflammation-Induced DepressionR21MH104694 · NIMH · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DANTZER, ROBERT · 2015 to 2016
$444k
NCI NIH HHS P30 CA016672NCI NIH HHS R01 CA193522NHLBI NIH HHS R01 HL129795NIMH NIH HHS R21 MH104694NINDS NIH HHS R01 NS073939
6 · The paper itself

Abstract

rationaleWhile the relationship between inflammation and depression is well-established, the molecular mechanisms mediating this relationship remain unclear. RNA sequencing analysis comparing brains of vehicle- and lipopolysaccharide-treated mice revealed LCN2 among the most dysregulated genes. As LCN2 is known to be an important regulator of the immune response to bacterial infection, we investigated its role in the behavioral response to lipopolysaccharide.

objectiveTo explore the role of LCN2 in modulating behavior following lipopolysaccharide administration using wild type (WT) and lcn2

methodsUsing a within-subjects design, mice were treated with 0.33 mg/kg liposaccharide (LPS) and vehicle. Primary outcome measures included body weight, food consumption, voluntary wheel running, sucrose preference, and the tail suspension test. To evaluate the inflammatory response, 1 week later, mice were re-administered either vehicle or LPS and terminated at 6 h.

resultsWhile lcn2

conclusionsOur data demonstrate that lcn2 is dispensable for sterile inflammation-induced sickness and depression-like behavior. Specifically, lcn2

Indexed as

AnimalsBrainCytokinesDepressionIllness BehaviorInflammationLipocalin-2LipopolysaccharidesMaleMiceMice, Inbred C57BLMice, KnockoutMotor ActivityCytokinesLipocalin-2LipopolysaccharidesDepressionInflammationInnate immunityLipocalin-2LipopolysaccharideSickness behavior

Identifiers

PMID30806746
PMCPMC6710168
OpenAlexW2917729267

What OpenQuestion holds

Textmetadata
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.