Evidence map›Paper›PMID 26100333›Full record

ArticleBrain research2015

Effects of co-administration of 2-arachidonylglycerol (2-AG) and a selective µ-opioid receptor agonist into the nucleus accumbens on high-fat feeding behaviors in the rat.

Kyle E Parker, Jordan G McCall, Sophia R McGuirk, Seema Trivedi, Dennis K Miller, Matthew J Will

Open access · greenAbstract read
In one paragraph

Article in Brain research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

3 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. 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 at 1 institution in 1 country.

Kyle E ParkerDepartment of Psychological Sciences, University of Missouri, Columbia, MO, United States; Christopher Bond Life Sciences Center, University of Missouri, Columbia, MO, United States; Interdisciplinary Neuroscience Program, University of Missouri, Columbia, MO, United States.
Jordan G McCallDepartment of Psychological Sciences, University of Missouri, Columbia, MO, United States; Christopher Bond Life Sciences Center, University of Missouri, Columbia, MO, United States.
Sophia R McGuirkDepartment of Psychological Sciences, University of Missouri, Columbia, MO, United States; Christopher Bond Life Sciences Center, University of Missouri, Columbia, MO, United States.
Seema TrivediDepartment of Psychological Sciences, University of Missouri, Columbia, MO, United States; Christopher Bond Life Sciences Center, University of Missouri, Columbia, MO, United States.
Dennis K MillerChristopher Bond Life Sciences Center, University of Missouri, Columbia, MO, United States.
Matthew J WillDepartment of Psychological Sciences, University of Missouri, Columbia, MO, United States; Christopher Bond Life Sciences Center, University of Missouri, Columbia, MO, United States. Electronic address: willm@missouri.edu.
University of Missouri · US

Funding

TRAINING GRANT IN DIABETES, ENDOCRINOLOGY, &METABOLISMT32DK007203 · NIDDK · UNIVERSITY OF MINNESOTA TWIN CITIES · PI LISA Senye CHOW, Douglas G Mashek · 1986 to 2026
$4.3M
Central opioids-cannabinoid interactions and food rewardR03DA024829 · NIDA · UNIVERSITY OF MISSOURI-COLUMBIA · PI WILL, MATTHEW J · 2008 to 2009
$140k
NIDA NIH HHS DA024829NIDA NIH HHS R03 DA024829NIDDK NIH HHS T32 DK007203
6 · The paper itself

Abstract

Previous research has demonstrated that the nucleus accumbens is a site where opioids and cannabinoids interact to alter feeding behavior. However, the influence of the endocannabinoid 2-arachidonylglycerol (2-AG) on the well-characterized model of intra-accumbens opioid driven high-fat feeding behavior has not been explored. The present experiments examined high-fat feeding associated behaviors produced by the interaction of 2-AG and the μ-opioid receptor agonist DAla(2),N,Me-Phe(4),Gly-ol(5)-enkaphalin (DAMGO) administered into the nucleus accumbens. Sprague-Dawley rats were implanted with bilateral cannulae aimed at the nucleus accumbens and were co-administered both a sub-threshold dose of 2-AG (0 or 0.25 μg/0.5 μl/side) and DAMGO (0, 0.025 μg or 0.25 μg/0.5 μl/side) in all dose combinations, and in a counterbalanced order. Animals were then immediately allowed a 2h-unrestricted access period to a palatable high-fat diet. Consumption, number and duration of food hopper entries, and locomotor activity were all monitored. DAMGO treatment led to an increase in multiple behaviors, including consumption, duration of food hopper entry, and locomotor activity. However, combined intra-accumbens administration of DAMGO and a subthreshold dose of 2-AG led to a significant increase in number of food hopper entries and locomotor activity, compared to DAMGO by itself. The results confirm that intra-accumbens administration of subthreshold dose of the endogenous cannabinoid 2-AG increases the DAMGO-induced approach and locomotor behaviors associated with high-fat feeding.

Indexed as

Analgesics, OpioidAnalysis of VarianceAnimalsArachidonic AcidsCannabinoid Receptor AgonistsDietary FatsEndocannabinoidsEnkephalin, Ala(2)-MePhe(4)-Gly(5)-Feeding BehaviorGlyceridesMaleMicroinjectionsNucleus AccumbensRatsRats, Sprague-DawleyAnalgesics, OpioidArachidonic AcidsCannabinoid Receptor AgonistsDietary FatsEndocannabinoidsEnkephalin, Ala(2)-MePhe(4)-Gly(5)-Glyceridesglyceryl 2-arachidonate2-arachidonylglycerolApproachCannabinoidConsumptionDAMGOFeedingHigh fatNucleus accumbensOpioidPalatable foodReward

Identifiers

PMID26100333
PMCPMC4522234
OpenAlexW766102754

What OpenQuestion holds

Textmetadata
LicenceTDM
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.