Evidence map›Paper›PMID 18725235›Full record

ReviewNeuropharmacology2009

Bidirectional translational research: Progress in understanding addictive diseases.

M J Kreek, S D Schlussman, B Reed, Y Zhang, D A Nielsen, O Levran, Y Zhou, E R Butelman

Open access · greenAbstract readReview
In one paragraph

Review in Neuropharmacology, 2009. 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
1.3field-weighted citation impact, top 24% 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.

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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

8 authors at 1 institution in 1 country.

M J KreekLaboratory of the Biology of Addictive Diseases, Rockefeller University, 1230 York Avenue, New York, NY 10065, USA. kreek@rockefeller.edu
S D Schlussman
B Reed
Y Zhang
D A Nielsen
O Levran
Y Zhou
E R Butelman
Rockefeller University · US

Funding

TRANSFORMING TRANSLATIONAL SCIENCE AND EDUCATION TO BENEFIT HUMAN HEALTHUL1RR024143 · NCRR · ROCKEFELLER UNIVERSITY · PI COLLER, BARRY · 2006 to 2011
$49.1M
ULTRASTUCTURE, RECEPTORS, AND GENE EXPRESSIONP60DA005130 · NIDA · ROCKEFELLER UNIVERSITY · PI KREEK, MARY J · 2002 to 2012
$30.6M
HIV and Psychiatric Comorbidity: Selected Genetic and Epigenetic FactorsR01MH079880 · NIMH · ROCKEFELLER UNIVERSITY · PI KREEK, MARY J · 2006 to 2010
$3.0M
Addictive Drugs-Pharmacology &PhysiologyK05DA000049 · NIDA · ROCKEFELLER UNIVERSITY · PI KREEK, MARY J · 1985 to 2007
$1.0M
SYSTEMICALLY ADMINISTERED DYNORPHINSR01DA011113 · NIDA · ROCKEFELLER UNIVERSITY · PI BUTELMAN, EDUARDO R · 1996 to 2002
$976k
kappa-agonist effects of the hallucinogen Salvinorin AR01DA017369 · NIDA · ROCKEFELLER UNIVERSITY · PI BUTELMAN, EDUARDO R · 2005 to 2008
$814k
DNA Methylation of Promoter CpG Dinucleotides in Opiate AddictionR03DA022266 · NIDA · ROCKEFELLER UNIVERSITY · PI NIELSEN, DAVID ANDREW · 2006 to 2007
$333k
NCRR NIH HHS UL1 RR024143NCRR NIH HHS UL1RR024143NIDA NIH HHS DA00049NIDA NIH HHS DA017369NIDA NIH HHS DA11113NIDA NIH HHS K05 DA000049NIDA NIH HHS P60 DA005130NIDA NIH HHS P60 DA05130NIDA NIH HHS R01 DA011113NIDA NIH HHS R03 DA022266NIDA NIH HHS R03 DA22266NIMH NIH HHS R01 MH079880NIMH NIH HHS R01MH-79880
6 · The paper itself

Abstract

The focus of this review is primarily on recent developments in bidirectional translational research on the addictions, within the Laboratory of the Biology of Addictive Diseases at The Rockefeller University. This review is subdivided into major interacting aspects, including (a) Investigation of neurobiological and molecular adaptations (e.g., in genes for the opioid receptors or endogenous neuropeptides) in response to cocaine or opiates, administered under laboratory conditions modeling chronic patterns of human self-exposure (e.g., chronic escalating "binge"). (b) The impact of such drug exposure on the hypothalamic-pituitary-adrenal (HPA) axis and interacting neuropeptidergic systems (e.g., opioid, orexin and vasopressin). (c) Molecular genetic association studies using candidate gene and whole genome approaches, to define particular systems involved in vulnerability to develop specific addictions, and response to pharmacotherapy. (d) Neuroendocrine challenge studies in normal volunteers and current addictive disease patients along with former addicts in treatment, to investigate differential pharmacodynamics and responsiveness of molecular targets, in particular those also investigated in the experimental and molecular genetic approaches as described above.

Indexed as

Substance-Related DisordersAnimalsBiomedical ResearchHumansHypothalamo-Hypophyseal SystemNarcoticsPituitary-Adrenal SystemReceptors, OpioidNarcoticsReceptors, Opioid

Identifiers

PMID18725235
PMCPMC2741728
OpenAlexW1989710212

What OpenQuestion holds

Textmetadata
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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.