Evidence map›Paper›PMID 27019746›Full record

ArticleFuture science OA2015

Development and therapeutic applications of nitric oxide releasing materials to treat erectile dysfunction.

Kelvin P Davies

Open access · goldAbstract read
In one paragraph

Article in Future science OA, 2015. 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
0.8field-weighted citation impact, top 26% 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

10 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Dietary supplements for improving nitric-oxide synthesis.Journal of preventive medicine and hygiene · 2022
    Review
  5. Article
  6. A visualization system for erectile vascular dynamics.Frontiers in cell and developmental biology · 2022
    Article
  7. Review
  8. Aqueous extract ofFood science and biotechnology · 2019
    Article
  9. Pharmacokinetics and Pharmacodynamics of Promising Arginase Inhibitors.European journal of drug metabolism and pharmacokinetics · 2017
    Review
  10. Review
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

1 author at 1 institution in 1 country.

Kelvin P DaviesAlbert Einstein College of Medicine, Forchheimer 742, 1300 Morris Park Ave, Bronx, NY 10461, USA.
Albert Einstein College of Medicine · US

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 R56 DK087872
6 · The paper itself

Abstract

The role of nitric oxide (NO) in erectile physiology is well documented. NO activates relaxation of corporal cavernosal smooth muscle tissue resulting in increased blood flow into the penis resulting in an erection. At present, pharmacologic treatments for erectile dysfunction, such as the phosphodiesterase-5 inhibitors, potentiate the erectile response generated by NO. However, a new class of treatments at a preclinical stage may allow localized delivery of NO to the penis via cutaneous application. These treatments may be of particular value to patients with a neurogenic component to their erectile dysfunction, and may act synergistically with phosphodiesterase-5 inhibitors to increase their efficacy.

Indexed as

EDerectile dysfunctionnanoparticlesnitric oxideNOPDE5 inhibitorsphosphodiesterase-5 inhibitors

Identifiers

PMID27019746
PMCPMC4806684
OpenAlexW2194772966

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.