Evidence map›Paper›PMID 23800036›Full record

ArticleJournal of thrombosis and haemostasis : JTH2013

Peptidergic regulation of plasminogen activator inhibitor-1 gene expression in vivo.

N A Gingles, H Bai, L A Miles, R J Parmer

Open access · greenAbstract read
In one paragraph

Article in Journal of thrombosis and haemostasis : JTH, 2013. 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, top 91% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

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 at 3 institutions in 1 country.

N A GinglesDepartment of Medicine, University of California San Diego, San Diego, CA, USA; Veterans Administration San Diego Healthcare System, San Diego, CA, USA.
H Bai
L A Miles
R J Parmer
University of California, San Diego · USScripps Research Institute · USVA San Diego Healthcare System · US

Funding

Regulation of plasminogen-dependent cell functions by the novel receptor, Plg-RKTR01HL081046 · NHLBI · SCRIPPS RESEARCH INSTITUTE, THE · PI MILES, LINDSEY A · 2007 to 2024
$8.7M
REGULATION OF THE PLASMINOGEN SYSTEMR01HL045934 · NHLBI · SCRIPPS RESEARCH INSTITUTE, THE · PI MILES, LINDSEY A · 1990 to 2006
$2.5M
A Novel Plasminogen Receptor in Breast CancerR01CA166473 · NCI · TORREY PINES INST FOR MOLECULAR STUDIES · PI MILES, LINDSEY A, MUELLER, BARBARA MARIA · 2012 to 2016
$2.1M
PROCESSING OF CHROMOGRANIN A BY THE FIBRINOLYTIC SYSTEMR01HL050398 · NHLBI · VETERANS MEDICAL RESEARCH FDN/SAN DIEGO · PI PARMER, ROBERT J · 1994 to 2001
$424k
Cell Surface Plasminogen Activation and HypertensionI01BX002026 · VA · VA SAN DIEGO HEALTHCARE SYSTEM · PI PARMER, ROBERT J · 2013 to 2016
–
BLRD VA I01 BX002026NCI NIH HHS R01 CA166473NHLBI NIH HHS HL-081046NHLBI NIH HHS HL-45934NHLBI NIH HHS HL-50398NHLBI NIH HHS R01 HL045934NHLBI NIH HHS R01 HL050398NHLBI NIH HHS R01 HL081046
6 · The paper itself

Abstract

backgroundThe mechanisms by which PAI-1 biosynthesis is altered during stress have not been fully elucidated. Studies suggest a major role for neuro-peptidergic modulation of the stress response by PACAP (pituitary adenylate cyclase-activating polypeptide), a member of the VIP/secretin/glucagon family.

objectiveWe tested the hypothesis that PACAP regulates PAI-1 biosynthesis during stress in vivo.

methodsPAI-1 gene expression was monitored by RT-PCR in adrenal glands harvested from C57BL/6J mice that were unstressed, or subjected to restraint stress for 2 h, or treated with PACAP.

resultsPAI-1 mRNA expression was markedly increased in adrenals from stressed mice. Restraint stress resulted in much smaller increments in adrenal tPA mRNA, suggesting that local adrenal tPA/PAI-1 biosynthetic balance is markedly altered by stress. The observed increases in PAI-1mRNA during stress were substantially blunted (55 ± 4%, P < 0.001) by pretreatment with the specific PACAP receptor antagonist, PACAP6-38, compared with pretreatment with vehicle. Administration of the agonist PACAP1-38 alone resulted in a dose-dependent increase in tissue PAI-1 mRNA. PACAP1-38 administration also resulted in substantial increases in plasma PAI-1 antigen and active PAI-1 concentrations that were significantly greater in male mice than in female mice.

conclusionsWe conclude that adrenal PAI-1 mRNA expression is markedly increased by stress, and that the PACAP peptidergic signaling pathway plays a major role in mediating the stress-induced increase in PAI-1 biosynthesis.

Indexed as

AnimalsBase SequenceDNA PrimersFemaleGene Expression RegulationMaleMiceMice, Inbred C57BLPituitary Adenylate Cyclase-Activating PolypeptidePlasminogen Activator Inhibitor 1Real-Time Polymerase Chain ReactionDNA PrimersPituitary Adenylate Cyclase-Activating PolypeptidePlasminogen Activator Inhibitor 1PhysiologicalPituitary adenylate cyclase-activating polypeptidePlasminogen activator inhibitor-1StressSympathetic Nervous Systemtissue plasminogen activator

Identifiers

PMID23800036
PMCPMC3965269
OpenAlexW2062436429

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.