Evidence map›Paper›PMID 25136404›Full record

ArticleOxidative medicine and cellular longevity2014

Anandamide protects HT22 cells exposed to hydrogen peroxide by inhibiting CB1 receptor-mediated type 2 NADPH oxidase.

Ji Jia, Lei Ma, Mingchun Wu, Lei Zhang, Xiajing Zhang, Qian Zhai, Tao Jiang, Qiang Wang, Lize Xiong

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 2 pooled it
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

33 citing papers in PubMed, 2 syntheses or guidelines pooled it, 57 citations in OpenAlex.

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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 2 institutions in 1 country.

Ji JiaDepartment of Anesthesiology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.
Lei MaDepartment of Anesthesiology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.ORCID 0000-0002-8559-3305
Mingchun WuDepartment of Anesthesiology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.
Lei ZhangDepartment of Anesthesiology, Xi'an No. 4 Hospital, Xi'an 710032, China.
Xiajing ZhangDepartment of Anesthesiology, Xi'an No. 4 Hospital, Xi'an 710032, China.
Qian ZhaiDepartment of Anesthesiology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.
Tao JiangDepartment of Anesthesiology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.
Qiang WangDepartment of Anesthesiology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.ORCID 0000-0002-3620-3446
Lize XiongDepartment of Anesthesiology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.
Xijing Hospital · CNWuhan No.1 Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEndogenous cannabinoid anandamide (AEA) protects neurons from oxidative injury in rodent models; however the mechanism of AEA-induced neuroprotection remains to be determined. Activation of neuronal NADPH oxidase 2 (Nox2) contributes to oxidative damage of the brain, and inhibition of Nox2 can attenuate cerebral oxidative stress. We aimed to determine whether the neuronal Nox2 was involved in protection mediated by AEA.

methodsThe mouse hippocampal neuron cell line HT22 was exposed to hydrogen peroxide (H2O2) to mimic oxidative injury of neurons. The protective effect of AEA was assessed by measuring cell metabolic activity, apoptosis, lactate dehydrogenase (LDH) release, cellular morphology, intracellular reactive oxygen species (ROS), and antioxidant and oxidant levels and Nox2 expression.

resultsHT22 cells exposed to H2O2 demonstrated morphological changes, decreased LDH release, reduced metabolic activity, increased levels of intracellular ROS and oxidized glutathione (GSSG), reduced levels of superoxide dismutase (SOD), and reduced glutathione (GSH) and increased expression of Nox2. AEA prevented these effects, a property abolished by simultaneous administration of CB1 antagonist AM251 or CB1-siRNA.

conclusionNox2 inhibition is involved in AEA-induced cytoprotection against oxidative stress through CB1 activation in HT22 cells.

Indexed as

AnimalsApoptosisArachidonic AcidsCannabinoid Receptor AgonistsCell LineEndocannabinoidsGlutathioneHippocampusHydrogen PeroxideL-Lactate DehydrogenaseMembrane GlycoproteinsMiceNADPH Oxidase 2NADPH OxidasesOxidative StressPolyunsaturated AlkamidesanandamideArachidonic AcidsCannabinoid Receptor AgonistsCybb protein, mouseEndocannabinoidsGlutathioneHydrogen PeroxideL-Lactate DehydrogenaseMembrane GlycoproteinsNADPH Oxidase 2NADPH OxidasesPolyunsaturated AlkamidesReactive Oxygen SpeciesReceptor, Cannabinoid, CB1RNA, Small InterferingSuperoxide Dismutase

Identifiers

PMID25136404
PMCPMC4127243
OpenAlexW2029683856

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.