Evidence map›Paper›PMID 21035185›Full record

ArticleNeuropeptides2011

Cardiac ischemia-reperfusion regulates sympathetic neuropeptide expression through gp130-dependent and independent mechanisms.

Eric N Alston, Diana C Parrish, Wohaib Hasan, Kevin Tharp, Laura Pahlmeyer, Beth A Habecker

Open access · greenAbstract read
In one paragraph

Article in Neuropeptides, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.2field-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

23 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Untangling Peripheral Sympathetic Neurocircuits.Frontiers in cardiovascular medicine · 2022
    Article
  6. Review
  7. Article
  8. Article
  9. Protective Effects of PACAP in Peripheral Organs.Frontiers in endocrinology · 2020
    Review
  10. Review
  11. Article
  12. Protective effects of PACAP in ischemia.The journal of headache and pain · 2018
    Review
  13. Article
  14. Article
  15. Review
  16. Myocardial Infarction Causes Transient Cholinergic Transdifferentiation of Cardiac Sympathetic Nerves via gp130.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016
    Article
  17. Article
  18. Article
  19. Article
  20. 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

6 authors at 1 institution in 1 country.

Eric N AlstonDepartment of Physiology and Pharmacology, Oregon Health and Science University, Portland, OR 97239, United States.
Diana C Parrish
Wohaib Hasan
Kevin Tharp
Laura Pahlmeyer
Beth A Habecker
Oregon Health & Science University · US

Funding

Regulation of Sympathetic Function by InfarctionR01HL068231 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI HABECKER, BETH A · 2001 to 2015
$4.3M
NHLBI NIH HHS HL068231NHLBI NIH HHS R01 HL068231
6 · The paper itself

Abstract

Cardiac function is regulated by a balance of sympathetic and parasympathetic transmission. Neuropeptide Y (NPY) and galanin (GAL) released from cardiac sympathetic neurons inhibits parasympathetic transmission in the heart. Sympathetic peptides may contribute to autonomic imbalance, which is characterized by increased sympathetic and decreased parasympathetic transmission and contributes to life threatening cardiovascular pathologies. Several gp130 cytokines are increased in the heart after myocardial infarction (MI), and these cytokines stimulate neuropeptide expression in sympathetic neurons. We used mice whose sympathetic neurons lack the gp130 receptor (gp130(DBH-Cre/lox) mice) to ask if cytokine activation of gp130 regulated neuropeptide expression in cardiac sympathetic nerves after MI. Myocardial infarction decreased NPY mRNA through a gp130 independent mechanism and increased VIP and PACAP mRNA via gp130, while GAL mRNA was unchanged. Immunohistochemistry revealed a gp130-dependent increase in PACAP38 in cells of the stellate ganglion after MI, and PACAP was detected in pre-ganglionic fibers of all genotypes and surgical groups. VIP was identified in a few sympathetic nerve fibers in all genotypes and surgical groups. GAL and PACAP38 were not detected in sham hearts, but peptide immunoreactivity was high in the infarct three days after MI. Surprisingly, peptides were abundant in cells that co-labeled with macrophage markers F4/80 and MAC2, but were not detected in sympathetic axons. PACAP protects cardiac myocytes from apoptosis, and GAL stimulates axon regeneration in addition to inhibiting parasympathetic transmission. Thus, these peptides may play an important role in cardiac and neuronal remodeling after ischemia-reperfusion.

Indexed as

AnimalsCytokine Receptor gp130GalaninHeartHumansMiceMice, Inbred C57BLMice, KnockoutMyocardial IschemiaMyocardiumNeuropeptidesNeuropeptide YPituitary Adenylate Cyclase-Activating PolypeptideReperfusion InjurySympathetic Nervous SystemVasoactive Intestinal PeptideCytokine Receptor gp130GalaninNeuropeptidesNeuropeptide YPituitary Adenylate Cyclase-Activating PolypeptideVasoactive Intestinal Peptide

Identifiers

PMID21035185
PMCPMC3053070
OpenAlexW1994719453

What OpenQuestion holds

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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.