Evidence map›Paper›PMID 25826533›Full record

ArticleInternational journal of molecular sciences2015

Elevated levels of endocannabinoids in chronic hepatitis C may modulate cellular immune response and hepatic stellate cell activation.

Eleonora Patsenker, Philip Sachse, Andrea Chicca, María Salomé Gachet, Vreni Schneider, Johan Mattsson, Christian Lanz, Mathias Worni, Andrea de Gottardi, Mariam Semmo and 6 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2015. 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
4.5field-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

26 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Current investigations for liver fibrosis treatment: between repurposing the FDA-approved drugs and the other emerging approaches.Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques · 2023
    Review
  7. Cannabinoids and Chronic Liver Diseases.International journal of molecular sciences · 2022
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. LncRNAs in HCV Infection and HCV-Related Liver Disease.International journal of molecular sciences · 2020
    Review
  14. Review
  15. Article
  16. Viruses · 2019
    Article
  17. Review
  18. Article
  19. Article
  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

16 authors at 5 institutions in 2 countries.

Eleonora PatsenkerDepartment of Clinical Research, University of Bern, Bern 3010, Switzerland. eleonora.patsenker@ikp.unibe.ch.
Philip SachseDepartment of Clinical Research, University of Bern, Bern 3010, Switzerland. sachsephilip@gmail.com.
Andrea ChiccaInstitute of Biochemistry and Molecular Medicine, University of Bern, Bern 3012, Switzerland. andrea.chicca@ibmm.unibe.ch.
María Salomé GachetInstitute of Biochemistry and Molecular Medicine, University of Bern, Bern 3012, Switzerland. maria.gachet@ibmm.unibe.ch.
Vreni SchneiderDepartment of Clinical Research, University of Bern, Bern 3010, Switzerland. vreni.schneider@ikp.unibe.ch.
Johan MattssonDepartment of Clinical Research, Laboratory of Phytopharmacology, Bioanalytics and Pharmacokinetics, University of Bern, Bern 3010, Switzerland. Johan.Mattsson@insel.ch.
Christian LanzDepartment of Clinical Research, Laboratory of Phytopharmacology, Bioanalytics and Pharmacokinetics, University of Bern, Bern 3010, Switzerland. christian.lanz@dkf.unibe.ch.
Mathias WorniDepartment of Visceral Surgery and Medicine, Inselspital, University of Bern, Bern 3010, Switzerland. christian.lanz@dkf.unibe.ch.
Andrea de GottardiDepartment of Visceral Surgery and Medicine, Inselspital, University of Bern, Bern 3010, Switzerland. andrea.degottardi@ikp.unibe.ch.
Mariam SemmoDepartment of Nephrology, Inselspital, University of Bern, Bern 3010, Switzerland. Mariam.Semmo@insel.ch.
Jochen HampeDepartment of Medicine II, Division of Gastroenterology, University of Dresden, Dresden 01307, Germany. jochen.hampe@uniklinikum-dresden.de.
Clemens SchafmayerDepartment of Visceral Surgery, University of Schleswig-Holstein, Campus Kiel, Kiel 24105, Germany. clemens.schafmayer@uksh-kiel.de.
Rudolf BrenneisenDepartment of Clinical Research, Laboratory of Phytopharmacology, Bioanalytics and Pharmacokinetics, University of Bern, Bern 3010, Switzerland. rudolf.brenneisen@dkf.unibe.ch.
Jürg GertschInstitute of Biochemistry and Molecular Medicine, University of Bern, Bern 3012, Switzerland. juerg.gertsch@ibmm.unibe.ch.
Felix StickelDepartment of Clinical Research, University of Bern, Bern 3010, Switzerland. felix.stickel@ikp.unibe.ch.
Nasser SemmoDepartment of Clinical Research, University of Bern, Bern 3010, Switzerland. nasser.semmo@insel.ch.
University of Bern · CHUniversity Hospital of Bern · CHBioanalytica (Switzerland) · CHKiel University · DETU Dresden · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The endocannabinoid (EC) system is implicated in many chronic liver diseases, including hepatitis C viral (HCV) infection. Cannabis consumption is associated with fibrosis progression in patients with chronic hepatitis C (CHC), however, the role of ECs in the development of CHC has never been explored. To study this question, anandamide (AEA) and 2-arachidonoyl glycerol (2-AG) were quantified in samples of HCV patients and healthy controls by gas and liquid chromatography mass spectrometry. Fatty acid amide hydrolase (FAAH) and monoaclyglycerol lipase (MAGL) activity was assessed by [3H]AEA and [3H]2-AG hydrolysis, respectively. Gene expression and cytokine release were assayed by TaqMan PCR and ELISpot, respectively. AEA and 2-AG levels were increased in plasma of HCV patients, but not in liver tissues. Hepatic FAAH and MAGL activity was not changed. In peripheral blood mononuclear cells (PBMC), ECs inhibited IFN-γ, TNF-α, and IL-2 secretion. Inhibition of IL-2 by endogenous AEA was stronger in PBMC from HCV patients. In hepatocytes, 2-AG induced the expression of IL-6, -17A, -32 and COX-2, and enhanced activation of hepatic stellate cells (HSC) co-cultivated with PBMC from subjects with CHC. In conclusion, ECs are increased in plasma of patients with CHC and might reveal immunosuppressive and profibrogenic effects.

Indexed as

AdultAmidohydrolasesArachidonic AcidsCells, CulturedCytokinesEndocannabinoidsFatty Acid Amide HydrolasesFemaleGlyceridesHepatic Stellate CellsHepatitis C, ChronicHumansImmunity, CellularMaleMiddle AgedMonoacylglycerol LipasesAmidohydrolasesanandamideArachidonic AcidsCytokinesEndocannabinoidsFatty Acid Amide HydrolasesGlyceridesglyceryl 2-arachidonateMonoacylglycerol LipasesPolyunsaturated Alkamides

Identifiers

PMID25826533
PMCPMC4425004
OpenAlexW2007522066

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.