Evidence map›Paper›PMID 22479453›Full record

ArticlePloS one2012

Methamphetamine increases LPS-mediated expression of IL-8, TNF-α and IL-1β in human macrophages through common signaling pathways.

Xun Liu, Peter S Silverstein, Vijeta Singh, Ankit Shah, Nilofer Qureshi, Anil Kumar

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

36 citing papers in PubMed, 59 citations in OpenAlex.

  1. Trial
  2. Article
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  4. Article
  5. Review
  6. Role of Microglia in Psychostimulant Addiction.Current neuropharmacology · 2023
    Review
  7. Review
  8. Review
  9. Article
  10. Methamphetamine Dysregulation of the Central Nervous System and Peripheral Immunity.The Journal of pharmacology and experimental therapeutics · 2021
    Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
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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

6 authors at 1 institution in 1 country.

Xun LiuDivision of Pharmacology and Toxicology, School of Pharmacy, School of Medicine, University of Missouri-Kansas City, Kansas City, Missouri, United States of America.
Peter S Silverstein
Vijeta Singh
Ankit Shah
Nilofer Qureshi
Anil Kumar
University of Missouri–Kansas City · US

Funding

MECHANISMS INVOLVED IN THE SEPTIC SHOCK SYNDROMER01GM050870 · NIGMS · UNIVERSITY OF WISCONSIN MADISON · PI QURESHI, NILOFER · 1994 to 2010
$3.4M
Methamphetamine and AIDS in a Non-Human Primate ModelR01DA025011 · NIDA · UNIVERSITY OF MISSOURI KANSAS CITY · PI KUMAR, ANIL · 2008 to 2014
$1.8M
HIV, Drug Abuse and NeurotoxicityR01DA025528 · NIDA · UNIVERSITY OF MISSOURI KANSAS CITY · PI KUMAR, ANIL · 2009 to 2013
$1.4M
NIDA NIH HHS DA025011NIDA NIH HHS DA025528NIDA NIH HHS R01 DA025011NIDA NIH HHS R01 DA025528NIGMS NIH HHS R01 GM050870
6 · The paper itself

Abstract

The use of methamphetamine (MA) has increased in recent years, and is a major health concern throughout the world. The use of MA has been associated with an increased risk of acquiring HIV-1, along with an increased probability of the acquisition of various sexually transmitted infections. In order to determine the potential effects of MA exposure in the context of an infectious agent, U937 macrophages were exposed to various combinations of MA and bacterial lipopolysaccharide (LPS). Treatment with MA alone caused significant increases in the levels of TNF-α, while treatment with both MA and LPS resulted in significant increases in TNF-α, IL-1β and the chemokine IL-8. The increases in cytokine or chemokine levels seen when cells were treated with both LPS and MA were generally greater than those increases observed when cells were treated with only LPS. Treatment with chemical inhibitors demonstrated that the signal transduction pathways including NF-kB, MAPK, and PI3-Akt were involved in mediating the increased inflammatory response. As discussed in the paper, these pathways appear to be utilized by both MA and LPS, in the induction of these inflammatory mediators. Since these pathways are involved in the induction of inflammation in response to other pathogens, this suggests that MA-exacerbated inflammation may be a common feature of infectious disease in MA abusers.

Indexed as

Signal TransductionCell LineCell NucleusHumansInflammation MediatorsInterleukin-1betaInterleukin-8LipopolysaccharidesMacrophagesMethamphetamineMitogen-Activated Protein KinasesNF-kappa B p50 SubunitPhosphatidylinositol 3-KinasesProtein TransportProto-Oncogene Proteins c-aktThiophenesInflammation MediatorsInterleukin-1betaInterleukin-8LipopolysaccharidesMethamphetamineMitogen-Activated Protein KinasesNF-kappa B p50 SubunitPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSC 514ThiophenesTumor Necrosis Factor-alpha

Identifiers

PMID22479453
PMCPMC3315580
OpenAlexW2079048484

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.