Evidence map›Paper›PMID 23885018›Full record

ArticleEndocrinology2013

The opposing roles of nitric oxide and cGMP in the age-associated decline in rat testicular steroidogenesis.

Srdjan J Sokanovic, Aleksandar Z Baburski, Marija M Janjic, Natasa J Stojkov, Maja M Bjelic, Dusan Lalosevic, Silvana A Andric, Stanko S Stojilkovic, Tatjana S Kostic

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Endocrinology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

12 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Cyclic guanosine monophosphate and 10-year change in left ventricular mass: the Multi-Ethnic Study of Atherosclerosis (MESA).Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals · 2021
    Article
  8. Review
  9. Article
  10. Aging has the opposite effect on cAMP and cGMP circadian variations in rat Leydig cells.Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology · 2017
    Article
  11. Article
  12. Leydig cell aging and hypogonadism.Experimental gerontology · 2015
    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

9 authors at 2 institutions in 2 countries.

Srdjan J SokanovicPhD, Reproductive Endocrinology and Signaling Group, University of Novi Sad, Novi Sad 21000, Serbia. tatjana.kostic@dbe.uns.ac.rs.
Aleksandar Z Baburski
Marija M Janjic
Natasa J Stojkov
Maja M Bjelic
Dusan Lalosevic
Silvana A Andric
Stanko S Stojilkovic
Tatjana S Kostic
University of Novi Sad · RSNational Institutes of Health · US

Funding

Intracellular Signaling In Endocrine CellsZIAHD000195 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI STOJILKOVIC, STANKO S. · 2009 to 2025
$18.8M
Intramural NIH HHS
6 · The paper itself

Abstract

The molecular mechanism of the aging-associated dysfunction of Leydig cells (LCs) is complex and poorly understood. In this study, we analyzed the contribution of nitric oxide (NO) and cGMP signaling to the age-dependent decline in LC function. Significant (>50%) decreases in serum, intratesticular, and LC androgens in aging rats (15-24 months) were accompanied by a proportional increase in NO production, an up-regulation of cGMP levels, and the expression of soluble guanylyl cyclase-1B and protein kinase G1 in LCs. In contrast, LC cAMP levels decreased with age, most likely reflecting the up-regulation of cAMP-specific phosphodiesterase expression. Moreover, the expression of genes encoding enzymes responsible for cholesterol transport and its conversion to T were reduced. Exposing LCs from aged animals to NO further increased cGMP levels and decreased cAMP and androgen production, whereas the addition of cell-permeable 8-bromoguanosine-cGMP alone had the opposite effect. In vivo inhibition of cGMP-specific phosphodiesterase-5 for 3 and 6 months in aged rats led to a partial restoration of androgens, NO, and cyclic nucleotide levels, as well as the expression of steroidogenic and NO/cGMP signaling genes. These results indicate that a progressive increase in NO production contributes to the age-dependent decrease in steroidogenesis in a cGMP-independent manner, whereas the sustained elevation in cGMP levels significantly slows the decline in LC function.

Indexed as

AgingSecond Messenger SystemsAndrogensAnimalsCells, CulturedCyclic AMPCyclic GMP-Dependent Protein Kinase Type ICyclic Nucleotide Phosphodiesterases, Type 5Fertility Agents, MaleGene Expression Regulation, DevelopmentalGuanylate CyclaseLeydig CellsMaleNitric OxidePhosphodiesterase 5 InhibitorsRatsAndrogensCyclic AMPCyclic GMP-Dependent Protein Kinase Type ICyclic Nucleotide Phosphodiesterases, Type 5Fertility Agents, MaleGuanylate CyclaseNitric OxidePde5a protein, mousePhosphodiesterase 5 InhibitorsPrkg1 protein, ratReceptors, Cytoplasmic and NuclearSoluble Guanylyl Cyclase

Identifiers

PMID23885018
PMCPMC3776867
OpenAlexW1965254593

What OpenQuestion holds

Textmetadata
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.