Evidence map›Paper›PMID 23108551›Full record

ReviewPhilosophical transactions of the Royal Society of London. Series B, Biological sciences2012

Endocannabinoids in neuroendopsychology: multiphasic control of mitochondrial function.

Alistair Nunn, Geoffrey Guy, Jimmy D Bell

Open access · bronzeAbstract readReview
In one paragraph

Review in Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Endocannabinoids in nervous system health and disease: the big picture in a nutshell.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2012
    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

3 authors at 3 institutions in 1 country.

Alistair NunnMetabolic and Molecular Imaging Group, MRC Clinical Sciences Centre, Imperial College London, Hammersmith Hospital, London W12 0NN, UK. a.nunn@imperial.ac.uk
Geoffrey Guy
Jimmy D Bell
GW Pharmaceuticals (United Kingdom) · GBHammersmith Hospital · GBImperial College London · GB

Funding

Medical Research Council MC_U120061305
6 · The paper itself

Abstract

The endocannabinoid system (ECS) is a construct based on the discovery of receptors that are modulated by the plant compound tetrahydrocannabinol and the subsequent identification of a family of nascent ligands, the 'endocannabinoids'. The function of the ECS is thus defined by modulation of these receptors-in particular, by two of the best-described ligands (2-arachidonyl glycerol and anandamide), and by their metabolic pathways. Endocannabinoids are released by cell stress, and promote both cell survival and death according to concentration. The ECS appears to shift the immune system towards a type 2 response, while maintaining a positive energy balance and reducing anxiety. It may therefore be important in resolution of injury and inflammation. Data suggest that the ECS could potentially modulate mitochondrial function by several different pathways; this may help explain its actions in the central nervous system. Dose-related control of mitochondrial function could therefore provide an insight into its role in health and disease, and why it might have its own pathology, and possibly, new therapeutic directions.

Indexed as

AnimalsApoptosisCalciumElectron TransportEndocannabinoidsEnergy MetabolismHumansInflammationInflammation MediatorsMitochondriaMitochondrial DiseasesNitric OxideNitric Oxide SynthaseNitric Oxide Synthase Type IIIReceptor, Cannabinoid, CB1TOR Serine-Threonine KinasesCalciumEndocannabinoidsInflammation MediatorsNitric OxideNitric Oxide SynthaseNitric Oxide Synthase Type IIIReceptor, Cannabinoid, CB1TOR Serine-Threonine Kinases

Identifiers

PMID23108551
PMCPMC3481535
OpenAlexW2156747199

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.