Evidence map›Paper›PMID 29504066›Full record

ArticleMetabolic brain disease2018

Anticonvulsive effects of endocannabinoids; an investigation to determine the role of regulatory components of endocannabinoid metabolism in the Pentylenetetrazol induced tonic- clonic seizures.

Parisa Zareie, Mehdi Sadegh, Mohammad Reza Palizvan, Homeira Moradi-Chameh

Abstract read
PubMed Publisher
In one paragraph

Article in Metabolic brain disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Efficacy of Phytocannabinoids in Epilepsy Treatment: Novel Approaches and Recent Advances.International journal of environmental research and public health · 2021
    Review
  9. DoesLaryngoscope investigative otolaryngology · 2020
    Review
  10. Article
  11. Review
  12. A Guide to Targeting the Endocannabinoid System in Drug Design.International journal of molecular sciences · 2020
    Review
  13. Review
  14. Druggable Targets in Endocannabinoid Signaling.Advances in experimental medicine and biology · 2020
    Review
  15. Article
  16. Article
  17. Effects of aqueous extract ofAvicenna journal of phytomedicine
    Article
  18. Protective effect ofAvicenna journal of phytomedicine
    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

4 authors at 2 institutions in 2 countries.

Parisa ZareieDepartment of Physiology, Faculty of Medicine, Arak University of Medical Sciences, Arak, Iran.
Mehdi SadeghDepartment of Physiology, Faculty of Medicine, Arak University of Medical Sciences, Arak, Iran. m.sadegh@arakmu.ac.ir.ORCID 0000-0001-5791-2463
Mohammad Reza PalizvanDepartment of Physiology, Faculty of Medicine, Arak University of Medical Sciences, Arak, Iran.
Homeira Moradi-ChamehDivision of Fundamental Neurobiology, Krembil Research Institute, Toronto, ON, Canada.
Arak University of Medical Sciences · IRKrembil Foundation · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

2-Arachidonoylglycerol (2-AG) and anandamide are two major endocannabinoids produced, released and eliminated by metabolic pathways. Anticonvulsive effect of 2-AG and CB1 receptor is well-established. Herein, we designed to investigate the anticonvulsive influence of key components of the 2-AG and anandamide metabolism. Tonic-clonic seizures were induced by an injection of Pentylenetetrazol (80 mg/kg, i.p.) in adult male Wistar rats. Delay and duration for the seizure stages were considered for analysis. Monoacylglycerol lipase blocker (JJKK048; 1 mg/kg) or alpha/beta hydroxylase domain 6 blocker (WWL70; 5 mg/kg) were administrated alone or with 2-AG to evaluate the anticonvulsive potential of these enzymes. To determine the CB1 receptor involvement, its blocker (MJ15; 3 mg/kg) was administrated associated with JJKK048 or WWL70. To assess anandamide anticonvulsive effect, anandamide membrane transporter blocker (LY21813240; 2.5 mg/kg) was used alone or associated with MJ15. Also, fatty acid amide hydrolase blocker (URB597; 1 mg/kg; to prevent intracellular anandamide hydrolysis) were used alone or with AMG21629 (transient receptor potential vanilloid; TRPV1 antagonist; 3 mg/kg). All compounds were dissolved in DMSO and injected i.p., before the Pentylenetetrazol. Both JJKK048 and WWL70 revealed anticonvulsive effect. Anticonvulsive effect of JJKK048 but not WWL70 was CB1 receptor dependent. LY2183240 showed CB1 receptor dependent anticonvulsive effect. However, URB597 revealed a TRPV1 dependent proconvulsive effect. It seems extracellular accumulation of 2-AG or anandamide has anticonvulsive effect through the CB1 receptor, while intracellular anandamide accumulation is proconvulsive through TRPV1.

Indexed as

AmidohydrolasesAnimalsArachidonic AcidsDisease Models, AnimalEndocannabinoidsFatty Acid Amide HydrolasesGlyceridesMalePentylenetetrazolePiperidinesPolyunsaturated AlkamidesRats, WistarReceptor, Cannabinoid, CB1SeizuresTRPV Cation ChannelsAmidohydrolasesanandamideArachidonic AcidsEndocannabinoidsFatty Acid Amide HydrolasesGlyceridesglyceryl 2-arachidonatePentylenetetrazolePiperidinesPolyunsaturated AlkamidesReceptor, Cannabinoid, CB1TRPV Cation Channels2-ArachidonoylglycerolABHD6AnandamideCB1 receptorMAGLRatTRPV1

Identifiers

PMID29504066
OpenAlexW2791704206

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.