Evidence map›Paper›PMID 23007622›Full record

ArticleThe journal of physiological sciences : JPS2013

Anandamide enhances expression of heat shock protein 72 to protect against ischemia-reperfusion injury in rat heart.

Qian Li, Min Shi, Bo Li

Open access · goldAbstract read
In one paragraph

Article in The journal of physiological sciences : JPS, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.3field-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

19 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
  5. Article
  6. Review
  7. Effects of Oleamide on the Vasomotor Responses in the Rat.Cannabis and cannabinoid research · 2020
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. The endocannabinoid system in cardiovascular function: novel insights and clinical implications.Clinical autonomic research : official journal of the Clinical Autonomic Research Society · 2018
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Autophagy, a process within reperfusion injury: an update.International journal of clinical and experimental pathology · 2014
    Review
  18. Review
  19. Review
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

3 authors at 2 institutions in 2 countries.

Qian LiDepartment of Physiology, Hebei Medical University, Shijiazhuang, 050017, China.
Min ShiDepartment of Clinical Laboratory, Second Hospital, Hebei Medical University, Shijiazhuang, 050000, China.
Bo LiDepartment of Clinical Laboratory, Shijiazhuang Center for Disease Control and Prevention, Shijiazhuang, 050011, China. liqian963@163.com.
Hebei Medical University · CNCenters for Disease Control and Prevention · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anandamide (AEA), one of endocannabinoids, has been reported to exhibit a cardioprotective ability to limit the damage produced by ischemia-reperfusion injury. AEA reportedly enhanced heat shock protein 72 (HSP72) and HSP25 expression in lungs to protect against lung inflammation. This study tested the hypothesis that intravenously injected AEA would induce HSP72 in the heart and thus render cardioprotection against ischemia-reperfusion injury in rats. Cardiac expression of HSPs was quantitatively evaluated in rats by Western blot analysis. That intravenously injected AEA 1 mg/kg in vivo induced expression of HSP72, which peaked at 24 h after administration. The enhancement of HSP72 by AEA was blocked by cannabinoid 2 (CB(2)) receptor antagonist AM630, but not cannabinoid 1 (CB(1)) receptor antagonist AM251. Therefore, the rats were induced with a 30-min coronary occlusion followed by a 120-min reperfusion in vivo at 24 h after administration of drugs or vehicle, and then the infarct size was measured. AEA reduced myocardial infarct size compared to control group. Pretreatment with AM630 but not AM251 abolished the infarct size-limiting effect of AEA. Further study demonstrated pretreatment with phosphatidylinositol 3-kinase (PI3K) inhibitor wortmannin, Akt inhibitor MK-2206 and AM630 attenuated phosphorylation of Akt and AEA-induced HSP72 expression. The results suggest that AEA is cardioprotective against ischemia-reperfusion insult through its induction of HSP72, which might be mediated by the PI3K/Akt signaling pathway. These effects were mediated by CB(2) but not CB(1) receptors.

Indexed as

AnimalsArachidonic AcidsEndocannabinoidsHeartHSP72 Heat-Shock ProteinsMaleMyocardial Reperfusion InjuryMyocardiumPhosphatidylinositol 3-KinasesPolyunsaturated AlkamidesProto-Oncogene Proteins c-aktRatsRats, Sprague-DawleyReceptor, Cannabinoid, CB1Receptor, Cannabinoid, CB2Reperfusion InjuryanandamideArachidonic AcidsEndocannabinoidsHSP72 Heat-Shock ProteinsPhosphatidylinositol 3-KinasesPolyunsaturated AlkamidesProto-Oncogene Proteins c-aktReceptor, Cannabinoid, CB1Receptor, Cannabinoid, CB2

Identifiers

PMID23007622
PMCPMC10717508
OpenAlexW2026504748

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.