Evidence map›Paper›PMID 24706617›Full record

ArticleAndrology2014

The effect of methamphetamine on an animal model of erectile function.

M T Tar, L R Martinez, J D Nosanchuk, K P Davies

Abstract read
In one paragraph

Article in Andrology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

M T TarDepartment of Urology, Albert Einstein College of Medicine, Bronx, NY, USA.
L R Martinez
J D Nosanchuk
K P Davies

Funding

Involvement of opiorphins and polyamine synthesis in the development of priapismR01DK087872 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI DAVIES, KELVIN P · 2011 to 2013
$738k
Opiorphin as a master regulator of pathways leading to priapismR56DK087872 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI DAVIES, KELVIN P · 2014 to 2014
$115k
NIDDK NIH HHS R01 DK087872NIDDK NIH HHS R01DK087872NIDDK NIH HHS R56 DK087872
6 · The paper itself

Abstract

In the US methamphetamine is considered a first-line treatment for attention-deficit hyperactivity disorder. It is also a common drug of abuse. Reports in patients and abusers suggest its use results in impotence. The efficacy of phosphodiesterase-5 inhibitors (PDE5i) to restore erectile function in these patient groups also has not been determined. In these studies, we determined if the rat is a suitable animal model for the physiological effects of methamphetamine on erectile function, and if a PDE5i (tadalafil) has an effect on erectile function following methamphetamine treatment. In acute phase studies, erectile function was measured in male Sprague-Dawley rats, before and after administration of 10 mg/kg methamphetamine i.p. Chronically treated animals received escalating doses of methamphetamine [2.5 mg/kg (1st week), 5 mg/kg (2nd week), and 10 mg/kg (3rd week)] i.p. daily for 3 weeks and erectile function compared with untreated controls. The effect of co-administration of tadalafil was also investigated in rats acutely and chronically treated with methamphetamine. Erectile function was determined by measuring the intracorporal pressure/blood pressure ratio (ICP/BP) following cavernous nerve stimulation. In both acute and chronic phase studies, we observed a significant increase in the rates of spontaneous erections after methamphetamine administration. In addition, following stimulation of the cavernous nerve at 4 and 6 mA, there was a significant decrease in the ICP/BP ratio (approximately 50%), indicative of impaired erectile function. Tadalafil treatment reversed this effect. In chronically treated animals, the ICP/BP ratio following 4 and 6 mA stimulation decreased by approximately 50% compared with untreated animals and erectile dysfunction (ED) was also reversed by tadalafil. Overall, our data suggest that the rat is a suitable animal model to study the physiological effect of methamphetamine on erectile function. Our work also provides a rationale for treating patients that report ED associated with therapeutics-containing methamphetamine or amphetamine with PDE5i.

Indexed as

AnimalsCarbolinesDisease Models, AnimalErectile DysfunctionMaleMethamphetaminePenile ErectionPhosphodiesterase 5 InhibitorsRats, Sprague-DawleyTadalafilCarbolinesMethamphetaminePhosphodiesterase 5 InhibitorsTadalafilerectile dysfunctionmethamphetaminerat modeltadalalfil

Identifiers

PMID24706617
PMCPMC4151273

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.