Evidence map›Paper›PMID 22989320›Full record

ArticleThe journal of sexual medicine2013

Analysis of erectile responses to BAY 41-8543 and muscarinic receptor stimulation in the rat.

George F Lasker, Edward A Pankey, Alexander V Allain, Jasdeep S Dhaliwal, Johannes-Peter Stasch, Subramanyam N Murthy, Philip J Kadowitz

Open access · greenAbstract read
In one paragraph

Article in The journal of sexual medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 17% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Analysis of erectile responses to H2S donors in the anesthetized rat.American journal of physiology. Heart and circulatory physiology · 2015
    Article
  6. Analysis of erectile responses to bradykinin in the anesthetized rat.American journal of physiology. Heart and circulatory physiology · 2015
    Article
  7. Article
  8. The sGC activator BAY 60-2770 has potent erectile activity in the rat.American journal of physiology. Heart and circulatory physiology · 2013
    Article
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

7 authors at 3 institutions in 2 countries.

George F LaskerDepartment of Pharmacology, Tulane University School of Medicine, New Orleans, LA 70112-2699, USA.
Edward A Pankey
Alexander V Allain
Jasdeep S Dhaliwal
Johannes-Peter Stasch
Subramanyam N Murthy
Philip J Kadowitz
Tulane University · USBayer (Germany) · DEUniversity of New Orleans · US

Funding

CARDIOPULMONARY SURGERY RESEARCHR01HL062000 · NHLBI · TULANE UNIVERSITY OF LOUISIANA · PI KADOWITZ, PHILIP J · 2000 to 2008
$2.5M
Stem Cell Therapy for Pulmonary HypertensionR01HL077421 · NHLBI · TULANE UNIVERSITY OF LOUISIANA · PI KADOWITZ, PHILIP J · 2005 to 2008
$1.9M
NHLBI NIH HHS HL62000NHLBI NIH HHS HL77421NHLBI NIH HHS R01 HL062000NHLBI NIH HHS R01 HL077421
6 · The paper itself

Abstract

introductionSoluble guanylate cyclase (sGC) is the receptor for nitric oxide (NO) and in pathophysiologic conditions where NO formation or bioavailability is impaired, erectile dysfunction (ED) occurs.

aimThe aim of this study was to investigate erectile responses to the sGC stimulator BAY 41-8543 in physiologic and pathophysiologic conditions.

methodsIncreases in intracavernosal pressure (ICP) in response to intracavernosal (ic) injections of BAY 41-8543 were investigated in the anesthetized rat.

main outcome measuresIncreases in ICP/MAP in response to ic injections of BAY 41-8543 and the interaction of BAY 41-8543 with exogenous and endogenously released NO were investigated and the effect of the sGC stimulator on cavernosal nerve injury was assessed. The mechanism of the increase in ICP/MAP in response to ic injection of acetylcholine was investigated.

resultsThe ic injections of BAY 41-8543 increased ICP/MAP and the duration of the response. BAY 41-8543 was less potent than sodium nitroprusside (SNP) and ic injections of BAY 41-8543 and SNP produced a larger response than the algebraic sum of responses to either agent alone. Simultaneous ic injection of BAY 41-8543 and cavernosal nerve stimulation produced a greater response than either intervention alone. Atropine and cavernosal nerve crush injury decreased the response to nerve stimulation and ic injection of BAY 41-8543 restored the response.

conclusionThese data show that BAY 41-8543 has significant erectile activity and can synergize with exogenous and endogenously released NO. This study shows that atropine and nerve crush attenuate the response to cavernosal nerve stimulation and that BAY 41-8543 can restore the response. The results with atropine, L-NAME and hexamethonium indicate that the response to ic injection of acetylcholine is mediated by muscarinic receptors and the release of NO with no significant role for nicotinic receptors. These results suggest that BAY 41-8543 would be useful in the treatment of ED.

Indexed as

Electric StimulationAcetylcholineAnimalsAtropineBlood PressureCholinergic AgonistsEnzyme InhibitorsHeart RateHexamethoniumInjectionsMaleMorpholinesNG-Nitroarginine Methyl EsterNicotinic AntagonistsNitric Oxide DonorsNitroprussideAcetylcholineAtropineBAY 41-8543Cholinergic AgonistsEnzyme InhibitorsHexamethoniumMorpholinesNG-Nitroarginine Methyl EsterNicotinic AntagonistsNitric Oxide DonorsNitroprussideParasympatholyticsPyrimidines

Identifiers

PMID22989320
PMCPMC3594361
OpenAlexW1957719936

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.