Evidence map›Paper›PMID 27207905›Full record

Trial reportThe international journal of neuropsychopharmacology2016

Subjective and Cardiovascular Effects of Intravenous Methamphetamine during Perindopril Maintenance: A Randomized, Double-Blind, Placebo-Controlled Human Laboratory Study.

Christopher D Verrico, Colin N Haile, Richard De La Garza, Kenneth Grasing, Thomas R Kosten, Thomas F Newton

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The international journal of neuropsychopharmacology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

9 citing papers in PubMed, 15 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

6 authors at 2 institutions in 1 country.

Christopher D VerricoMenninger Department of Psychiatry and Behavioral Sciences (Drs Verrico, Haile, De La Garza, Kosten, and Newton), Department of Pharmacology (Drs Verrico, De La Garza, Kosten, and Newton), and Department of Neuroscience (Drs De La Garza and Kosten), Baylor College of Medicine, Houston, TX; Department of Veterans Affairs Medical Center, Kansas City, Missouri (Dr Grasing); University of Kansas School of Medicine, Kansas City, Missouri (Dr Grasing). verrico@bcm.edu.
Colin N HaileMenninger Department of Psychiatry and Behavioral Sciences (Drs Verrico, Haile, De La Garza, Kosten, and Newton), Department of Pharmacology (Drs Verrico, De La Garza, Kosten, and Newton), and Department of Neuroscience (Drs De La Garza and Kosten), Baylor College of Medicine, Houston, TX; Department of Veterans Affairs Medical Center, Kansas City, Missouri (Dr Grasing); University of Kansas School of Medicine, Kansas City, Missouri (Dr Grasing).
Richard De La GarzaMenninger Department of Psychiatry and Behavioral Sciences (Drs Verrico, Haile, De La Garza, Kosten, and Newton), Department of Pharmacology (Drs Verrico, De La Garza, Kosten, and Newton), and Department of Neuroscience (Drs De La Garza and Kosten), Baylor College of Medicine, Houston, TX; Department of Veterans Affairs Medical Center, Kansas City, Missouri (Dr Grasing); University of Kansas School of Medicine, Kansas City, Missouri (Dr Grasing).
Kenneth GrasingMenninger Department of Psychiatry and Behavioral Sciences (Drs Verrico, Haile, De La Garza, Kosten, and Newton), Department of Pharmacology (Drs Verrico, De La Garza, Kosten, and Newton), and Department of Neuroscience (Drs De La Garza and Kosten), Baylor College of Medicine, Houston, TX; Department of Veterans Affairs Medical Center, Kansas City, Missouri (Dr Grasing); University of Kansas School of Medicine, Kansas City, Missouri (Dr Grasing).
Thomas R KostenMenninger Department of Psychiatry and Behavioral Sciences (Drs Verrico, Haile, De La Garza, Kosten, and Newton), Department of Pharmacology (Drs Verrico, De La Garza, Kosten, and Newton), and Department of Neuroscience (Drs De La Garza and Kosten), Baylor College of Medicine, Houston, TX; Department of Veterans Affairs Medical Center, Kansas City, Missouri (Dr Grasing); University of Kansas School of Medicine, Kansas City, Missouri (Dr Grasing).
Thomas F NewtonMenninger Department of Psychiatry and Behavioral Sciences (Drs Verrico, Haile, De La Garza, Kosten, and Newton), Department of Pharmacology (Drs Verrico, De La Garza, Kosten, and Newton), and Department of Neuroscience (Drs De La Garza and Kosten), Baylor College of Medicine, Houston, TX; Department of Veterans Affairs Medical Center, Kansas City, Missouri (Dr Grasing); University of Kansas School of Medicine, Kansas City, Missouri (Dr Grasing).
Baylor College of Medicine · USVeterans Health Administration · US

Funding

An ACE Inhibitor as a Treatment for Methamphetamine DependenceR01DA023468 · NIDA · BAYLOR COLLEGE OF MEDICINE · PI NEWTON, THOMAS FREDERICK · 2008 to 2012
$1.9M
NIDA NIH HHS R01 DA023468
6 · The paper itself

Abstract

backgroundOur pilot study suggested that the angiotensin-converting enzyme inhibitor perindopril might reduce some subjective effects produced by i.v. methamphetamine. We characterized the impact of a wider range of perindopril doses on methamphetamine-induced effects in a larger group of non-treatment-seeking, methamphetamine-using volunteers.

methodsBefore treatment, participants received 30mg methamphetamine. After 5 to 7 days of perindopril treatment (0, 4, 8, or 16mg/d), participants received 15 and 30mg of methamphetamine on alternate days. Before and after treatment, participants rated subjective effects and cardiovascular measures were collected.

resultsPrior to treatment with perindopril, there were no significant differences between treatment groups on maximum or peak subjective ratings or on peak cardiovascular effects. Following perindopril treatment, there were significant main effects of treatment on peak subjective ratings of "anxious" and "stimulated"; compared to placebo treatment, treatment with 8mg perindopril significantly reduced peak ratings of both anxious (P=.0009) and stimulated (P=.0070). There were no significant posttreatment differences between groups on peak cardiovascular effects.

conclusionsModerate doses of perindopril (8mg) significantly reduced peak subjective ratings of anxious and stimulated as well as attenuated many other subjective effects produced by methamphetamine, likely by inhibiting angiotensin II synthesis. Angiotensin II is known to facilitate the effects of norepinephrine, which contributes to methamphetamine's subjective effects. The lack of a classic dose-response function likely results from either nonspecific effects of perindopril or from between-group differences that were not accounted for in the current study (i.e., genetic variations and/or caffeine use). The current findings suggest that while angiotensin-converting enzyme inhibitors can reduce some effects produced by methamphetamine, more consistent treatment effects might be achieved by targeting components of the renin-angiotensin system that are downstream of angiotensin-converting enzyme.

Indexed as

Administration, IntravenousAdolescentAdultAngiotensin-Converting Enzyme InhibitorsAnxietyBlood PressureCentral Nervous System StimulantsDose-Response Relationship, DrugDouble-Blind MethodDrug UsersFemaleHealthy VolunteersHeart RateHumansMaleMethamphetamineAngiotensin-Converting Enzyme InhibitorsCentral Nervous System StimulantsMethamphetaminePerindoprilhuman laboratory studymethamphetaminerenin-angiotensin system

Identifiers

PMID27207905
PMCPMC4966279
OpenAlexW2327282490

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.