Evidence map›Paper›PMID 22215206›Full record

ArticleNaunyn-Schmiedeberg's archives of pharmacology2012

Cannabinoid CB1 receptor activation, pharmacological blockade, or genetic ablation affects the function of the muscarinic auto- and heteroreceptor.

Kirsten Schulte, Nina Steingrüber, Bernd Jergas, Agnes Redmer, Christina Maria Kurz, Rainer Buchalla, Beat Lutz, Andreas Zimmer, Eberhard Schlicker

Abstract read
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In one paragraph

Article in Naunyn-Schmiedeberg's archives of pharmacology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

11 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Up-regulation of CBFrontiers in neuroanatomy · 2022
    Article
  5. Intermittent ethanol exposure during adolescence impairs cannabinoid type 1 receptor-dependent long-term depression and recognition memory in adult mice.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2020
    Article
  6. N-Ethylmaleimide differentiates between the MNaunyn-Schmiedeberg's archives of pharmacology · 2018
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. 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

9 authors at 2 institutions in 1 country.

Kirsten SchulteInstitute of Pharmacology and Toxicology, BMZ, University of Bonn, Sigmund-Freud-Str. 25, 53105, Bonn, Germany.
Nina Steingrüber
Bernd Jergas
Agnes Redmer
Christina Maria Kurz
Rainer Buchalla
Beat Lutz
Andreas Zimmer
Eberhard Schlicker
University of Bonn · DEUniversity Medical Center of the Johannes Gutenberg University Mainz · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Different types of presynaptic inhibitory Gα(i/o) protein-coupled receptors usually do not act independently of each other but rather pre-activation of receptor X impairs the effect mediated via receptor Y. It is, however, unknown whether this interaction extends to the cannabinoid CB(1) receptor on cholinergic neurones and hence we studied whether its activation, pharmacological blockade, or genetic inactivation affects the function of other presynaptic inhibitory receptors. The electrically evoked acetylcholine or noradrenaline release was determined in superfused rodent tissues preincubated with (3)H-choline or (3)H-noradrenaline. The muscarinic M(2) receptor, Gα(i), and Gα(o) proteins were determined in hippocampal synaptosomes by Western blotting. Hippocampal anandamide and 2-arachidonoyl glycerol levels were determined by LC-MS/MS. The inhibitory effect of the muscarinic receptor agonist oxotremorine on acetylcholine release in hippocampal slices was increased by genetic CB(1) receptor ablation (mouse) and the CB(1) antagonist rimonabant (rat but not mouse) and decreased by a cannabinoid receptor agonist (mouse). In mouse tissues, CB(1) receptor ablation also increased the effect of a δ opioid receptor agonist on acetylcholine release in the hippocampus and the effect of oxotremorine on noradrenaline release in the vas deferens. CB(1) receptor ablation, to a very slight extent, increased Gα(o) protein levels without affecting either Gα(i) and M(2) receptor protein or the levels of anandamide and 2-arachidonoyl glycerol in the hippocampus. In conclusion, the CB(1) receptor shows an inhibitory interaction with the muscarinic and δ opioid receptor on cholinergic neurones in the rodent hippocampus and with the muscarinic receptor on noradrenergic neurones in the mouse vas deferens.

Indexed as

Analgesics, OpioidAnimalsArachidonic AcidArachidonic AcidsCerebral CortexCholinergic NeuronsEndocannabinoidsEnkephalin, D-Penicillamine (2,5)-GlyceridesGTP-Binding Protein alpha SubunitsHippocampusMaleMiceMice, Inbred C57BLMice, KnockoutMuscarinic AgonistsAnalgesics, OpioidanandamideArachidonic AcidArachidonic AcidsEndocannabinoidsEnkephalin, D-Penicillamine (2,5)-Glyceridesglyceryl 2-arachidonateGTP-Binding Protein alpha SubunitsMuscarinic AgonistsOxotremorinePiperidinesPolyunsaturated AlkamidesPyrazolesReceptor, Cannabinoid, CB1Receptors, MuscarinicReceptors, Opioid, deltaRimonabant

Identifiers

PMID22215206
OpenAlexW2149016099

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.