Evidence map›Paper›PMID 17043671›Full record

ArticleBritish journal of pharmacology2006

Anandamide mediates hyperdynamic circulation in cirrhotic rats via CB(1) and VR(1) receptors.

L Moezi, S A Gaskari, H Liu, S K Baik, A R Dehpour, S S Lee

Abstract read
In one paragraph

Article in British journal of pharmacology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
–field-weighted citation impact
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.

  1. Article
  2. Hepatic targeting of the centrally active cannabinoid 1 receptor (CBJournal of controlled release : official journal of the Controlled Release Society · 2023
    Article
  3. Review
  4. Article
  5. Article
  6. Vascular syndromes in liver cirrhosis.Clinical journal of gastroenterology · 2019
    Review
  7. Review
  8. Article
  9. Cardiohepatic syndrome.Current heart failure reports · 2015
    Review
  10. Article
  11. Pathophysiology of portal hypertension.Clinics in liver disease · 2014 · on this map
    Review
  12. Review
  13. Review
  14. Why do cannabinoid receptors have more than one endogenous ligand?Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2012
    Review
  15. Review
  16. Article
  17. Recent advances in the understanding of the role of the endocannabinoid system in liver diseases.Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver · 2011
    Review
  18. Endocannabinoids in liver disease.Hepatology (Baltimore, Md.) · 2011
    Review
  19. Article
  20. 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

6 authors.

L MoeziLiver Unit, Department of Medicine, University of Calgary, Calgary, Alberta, Canada.
S A Gaskari
H Liu
S K Baik
A R Dehpour
S S Lee

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeHyperdynamic circulation and mesenteric hyperaemia are found in cirrhosis. To delineate the role of endocannabinoids in these changes, we examined the cardiovascular effects of anandamide, AM251 (CB(1) antagonist), AM630 (CB(2) antagonist) and capsazepine (VR1 antagonist), in a rat model of cirrhosis. EXPERIMENTAL APPROACH: Cirrhosis was induced by bile duct ligation. Controls underwent sham operation. Four weeks later, diameters of mesenteric arteriole and venule (intravital microscopy), arterial pressure, cardiac output, systemic vascular resistance and superior mesenteric artery (SMA) flow were measured after anandamide, AM251 (with or without anandamide), AM630 and capsazepine administration. CB(1), CB(2) and VR1 receptor expression in SMA was assessed by western blot and RT-PCR. KEY

resultsAnandamide increased mesenteric vessel diameter and flow, and cardiac output in cirrhotic rats, but did not affect controls. Anandamide induced a triphasic arterial pressure response in controls, but this pattern differed markedly in cirrhotic rats. Pre-administration of AM251 blocked the effects of anandamide. AM251 (without anandamide) increased arterial pressure and systemic vascular resistance, constricted mesenteric arterioles, decreased SMA flow and changed cardiac output in a time-dependent fashion in cirrhotic rats. Capsazepine decreased cardiac output and mesenteric arteriolar diameter and flow, and increased systemic vascular resistance in cirrhotic rats, but lacked effect in controls. Expression of CB(1) and VR1 receptor proteins were increased in cirrhotic rats. AM630 did not affect any cardiovascular parameter in either group. CONCLUSIONS AND IMPLICATIONS: These data suggest that endocannabinoids contribute to hyperdynamic circulation and mesenteric hyperaemia in cirrhosis, via CB(1)- and VR1-mediated mechanisms.

Indexed as

AnimalsArachidonic AcidsBile DuctsBlood Flow VelocityBlood PressureBlotting, WesternCapsaicinCardiac OutputDisease Models, AnimalEndocannabinoidsHyperemiaIndolesLiver CirculationLiver Cirrhosis, BiliaryMaleMesenteric Artery, SuperiorAM 251anandamideArachidonic AcidsCapsaicincapsazepineEndocannabinoidsIndolesiodopravadolinePiperidinesPolyunsaturated AlkamidesPyrazolesReceptor, Cannabinoid, CB1Receptor, Cannabinoid, CB2RNA, MessengerTRPV1 receptorTRPV Cation ChannelsVasodilator Agents

Identifiers

PMID17043671
PMCPMC2014695

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.