Evidence map›Paper›PMID 27872594›Full record

ArticleFrontiers in pharmacology2016

Modafinil Induces Rapid-Onset Behavioral Sensitization and Cross-Sensitization with Cocaine in Mice: Implications for the Addictive Potential of Modafinil.

Raphael Wuo-Silva, Daniela F Fukushiro, André W Hollais, Renan Santos-Baldaia, Elisa Mári-Kawamoto, Laís F Berro, Thaís S Yokoyama, Leonardo B Lopes-Silva, Carolina S Bizerra, Roberta Procópio-Souza and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

7 citing papers in PubMed, 19 citations in OpenAlex.

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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

15 authors at 2 institutions in 1 country.

Raphael Wuo-SilvaLaboratory of Neurophysiology, Department of Physiology, Universidade Federal de São PauloSão Paulo, Brazil; Department of Pharmacology, Universidade Federal de São PauloSão Paulo, Brazil.
Daniela F FukushiroDepartment of Pharmacology, Universidade Federal de São Paulo São Paulo, Brazil.
André W HollaisDepartment of Pharmacology, Universidade Federal de São Paulo São Paulo, Brazil.
Renan Santos-BaldaiaDepartment of Pharmacology, Universidade Federal de São Paulo São Paulo, Brazil.
Elisa Mári-KawamotoDepartment of Pharmacology, Universidade Federal de São Paulo São Paulo, Brazil.
Laís F BerroDepartment of Psychobiology, Universidade Federal de São Paulo São Paulo, Brazil.
Thaís S YokoyamaLaboratory of Neurophysiology, Department of Physiology, Universidade Federal de São Paulo São Paulo, Brazil.
Leonardo B Lopes-SilvaDepartment of Psychobiology, Universidade Federal de São Paulo São Paulo, Brazil.
Carolina S BizerraDepartment of Pharmacology, Universidade Federal de São Paulo São Paulo, Brazil.
Roberta Procópio-SouzaDepartment of Pharmacology, Universidade Federal de São Paulo São Paulo, Brazil.
Debora HashiguchiLaboratory of Neurophysiology, Department of Physiology, Universidade Federal de São Paulo São Paulo, Brazil.
Lilian A FigueiredoLaboratory of Neurophysiology, Department of Physiology, Universidade Federal de São Paulo São Paulo, Brazil.
Jose L CostaFaculty of Pharmaceutical Sciences, Universidade Estadual de Campinas Campinas, Brazil.
Roberto Frussa-FilhoDepartment of Pharmacology, Universidade Federal de São Paulo São Paulo, Brazil.
Beatriz M LongoLaboratory of Neurophysiology, Department of Physiology, Universidade Federal de São Paulo São Paulo, Brazil.
Universidade Federal de São Paulo · BRUniversidade Estadual de Campinas (UNICAMP) · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is substantial controversy about the addictive potential of modafinil, a wake-promoting drug used to treat narcolepsy, proposed as pharmacotherapy for cocaine abuse, and used indiscriminately by healthy individuals due to its positive effects on arousal and cognition. The rapid-onset type of behavioral sensitization (i.e., a type of sensitization that develops within a few hours from the drug priming administration) has been emerged as a valuable tool to study binge-like patterns of drug abuse and the neuroplastic changes that occur quickly after drug administration that ultimately lead to drug abuse. Our aim was to investigate the possible development of rapid-onset behavioral sensitization to modafinil and bidirectional rapid-onset cross-sensitization with cocaine in male Swiss mice. A priming injection of a high dose of modafinil (64 mg/kg) induced rapid-onset behavioral sensitization to challenge injections of modafinil at the doses of 16, 32, and 64 mg/kg, administered 4 h later. Furthermore, rapid-onset cross-sensitization was developed between modafinil and cocaine (64 mg/kg modafinil and 20 mg/kg cocaine), in a bidirectional way. These results were not due to residual levels of modafinil as the behavioral effects of the priming injection of modafinil were no longer present and modafinil plasma concentration was reduced at 4 h post-administration. Taken together, the present findings provide preclinical evidence that modafinil can be reinforcing

Indexed as

cocainedrug abusemicemodafinilopen fieldrapid-onset behavioral sensitization

Identifiers

PMID27872594
PMCPMC5097917
OpenAlexW2546472556

What OpenQuestion holds

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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.