Evidence map›Paper›PMID 23307070›Full record

ArticlePsychopharmacology2013

Escalation of i.v. cocaine intake in peri-adolescent vs. adult rats selectively bred for high (HiS) vs. low (LoS) saccharin intake.

Nathan A Holtz, Marilyn E Carroll

Abstract read
In one paragraph

Article in Psychopharmacology, 2013. 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
–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

10 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Modeling the development of drug addiction in male and female animals.Pharmacology, biochemistry, and behavior · 2018
    Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. 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

2 authors.

Nathan A HoltzDepartment of Psychiatry, University of Minnesota Medical School, MMC 392, Minneapolis, MN 55455, USA. holt0324@umn.edu
Marilyn E Carroll

Funding

HIV Prevention Program among Substance Abusing SMIR01DA015627 · NIDA · UNIVERSITY OF PENNSYLVANIA · PI BLANK, MICHAEL B · 2003 to 2007
$3.2M
PRECLINICAL STUDIES:ANIMAL MODELS OF IMPULSIVITY AND ADDICTIONP20DA024196 · NIDA · UNIVERSITY OF MINNESOTA · PI LIM, KELVIN O. · 2007 to 2010
$3.2M
Vulnerability to Drug Abuse: Experimental InterventionsR01DA003240 · NIDA · UNIVERSITY OF MINNESOTA TWIN CITIES · PI CARROLL, MARILYN E. · 1985 to 2010
$3.1M
Models for the Prevention and Treatment of Drug AbuseK05DA015267 · NIDA · UNIVERSITY OF MINNESOTA TWIN CITIES · PI CARROLL, MARILYN E. · 2002 to 2011
$1.3M
ENVIRONMENTAL AND PHARMACOLOGICAL CONTROL OF DRUG ABUSER37DA003240 · NIDA · UNIVERSITY OF MINNESOTA TWIN CITIES · PI CARROLL, MARILYN E. · 1991 to 2000
$48k
NIDA NIH HHS K05 DA015267NIDA NIH HHS K05 DA015627NIDA NIH HHS P20 DA024196NIDA NIH HHS R01 DA003240NIDA NIH HHS R01 DA015627NIDA NIH HHS R37 DA003240
6 · The paper itself

Abstract

rationaleAdolescence marks a period of increased vulnerability to the development of substance use disorders. High sweet preference is a genetically mediated behavioral trait that also predicts vulnerability to substances of abuse. Previous research has shown that while adolescent rats selectively bred for high (HiS) saccharin intake acquire cocaine self-administration at the same rate as adult HiS rats, adolescent rats bred for low saccharin intake (LoS) acquire cocaine self-administration faster than adult LoS rats.

objectivesThis study was conducted to investigate the interaction of the addiction vulnerability factors of peri-adolescence and saccharin preference on cocaine intake using an animal model of escalation of cocaine consumption over 6-h/day sessions.

methodsPeri-adolescent and adult HiS and LoS female rats self-administered i.v. cocaine (0.4 mg/kg/inf) during short-access (2-h/day) sessions for 2 days. Next, a long-access (6-h/day) period (LgA) commenced and lasted 16 days. Following LgA, session length was returned to 2-h/day for a second short access phase.

resultsLoS peri-adolescent rats escalated cocaine intake over the LgA period and consumed more drug than LoS adult rats; however, peri-adolescent and adult HiS rats consumed similar amounts of cocaine during this period. Additionally, adult HiS rats self-administered more cocaine than adult LoS rats during the LgA period, while there was no phenotypic difference between the rat lines during peri-adolescence for the LgA period. During the first short-access phase, peri-adolescent rats self-administered more cocaine than adult rats.

conclusionsThese results emphasize the importance of adolescent drug abuse prevention by illustrating that phenotypic protection from addiction may not be expressed until adulthood.

Indexed as

Behavior, AddictiveAge FactorsAnimalsBehavior, AnimalCocaineCocaine-Related DisordersFemaleInjections, IntravenousRatsRats, Sprague-DawleySaccharinSelf AdministrationTime FactorsCocaineSaccharin

Identifiers

PMID23307070
PMCPMC4583775

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Registered trials

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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.