Evidence map›Paper›PMID 36232988›Full record

ArticleInternational journal of molecular sciences2022

Mechanisms Underlining Inflammatory Pain Sensitivity in Mice Selected for High and Low Stress-Induced Analgesia-The Role of Endocannabinoids and Microglia.

Piotr Poznanski, Joanna Giebultowicz, Justyna Durdzinska, Tomasz Kocki, Mariusz Sacharczuk, Magdalena Bujalska-Zadrozny, Anna Lesniak

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 30% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 5 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. 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

7 authors at 3 institutions in 1 country.

Piotr PoznanskiDepartment of Experimental Genomics, Institute of Genetics and Animal Biotechnology, Polish Academy of Sciences in Jastrzebiec, Postepu 36A Str., 05-552 Magdalenka, Poland.ORCID 0000-0002-1321-2235
Joanna GiebultowiczDepartment of Bioanalysis and Drugs Analysis, Faculty of Pharmacy, Medical University of Warsaw, Centre for Preclinical Research and Technology, Banacha 1 Str., 02-097 Warsaw, Poland.ORCID 0000-0002-2567-4453
Justyna DurdzinskaDepartment of Pharmacodynamics, Faculty of Pharmacy, Medical University of Warsaw, Banacha 1 Str., 02-097 Warsaw, Poland.
Tomasz KockiDepartment of Experimental and Clinical Pharmacology, Medical University of Lublin, Jaczewskiego 8b Str., 20-090 Lublin, Poland.ORCID 0000-0002-7587-2626
Mariusz SacharczukDepartment of Experimental Genomics, Institute of Genetics and Animal Biotechnology, Polish Academy of Sciences in Jastrzebiec, Postepu 36A Str., 05-552 Magdalenka, Poland.
Magdalena Bujalska-ZadroznyDepartment of Pharmacodynamics, Faculty of Pharmacy, Medical University of Warsaw, Banacha 1 Str., 02-097 Warsaw, Poland.
Anna LesniakDepartment of Pharmacodynamics, Faculty of Pharmacy, Medical University of Warsaw, Banacha 1 Str., 02-097 Warsaw, Poland.
Medical University of Warsaw · PLMedical University of Lublin · PLPolish Academy of Sciences · PL

Funding

Institute of Genetics and Animal Biotechnology S.I.1.3Medical University of Warsaw FW3/PM1/17
6 · The paper itself

Abstract

In this work we strived to determine whether endocannabinoid system activity could account for the differences in acute inflammatory pain sensitivity in mouse lines selected for high (HA) and low (LA) swim-stress-induced analgesia (SSIA). Mice received intraplantar injections of 5% formalin and the intensity of nocifensive behaviours was scored. To assess the contribution of the endocannabinoid system, mice were intraperitoneally (i.p.) injected with rimonabant (0.3-3 mg/kg) prior to formalin. Minocycline (45 and 100 mg/kg, i.p.) was administered to investigate microglial activation. The possible involvement of the endogenous opioid system was investigated with naloxone (1 mg/kg, i.p.). Cannabinoid receptor types 1 and 2 (

Indexed as

AnalgesiaEndocannabinoidsAnalgesics, OpioidAnimalsArachidonic AcidsChromatography, LiquidFormaldehydeMiceMicrogliaMinocyclineNaloxonePainPain ThresholdPolyunsaturated AlkamidesReceptors, CannabinoidReceptors, OpioidAnalgesics, OpioidanandamideArachidonic AcidsEndocannabinoidsFormaldehydeMinocyclineNaloxonePolyunsaturated AlkamidesReceptors, CannabinoidReceptors, OpioidRimonabant2-arachidonoylglycerolanandamideHA/LA micemicrogliareceptor expression

Identifiers

PMID36232988
PMCPMC9570076
OpenAlexW4303699376

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.