Evidence map›Paper›PMID 22502863›Full record

ArticleAutonomic neuroscience : basic & clinical2012

Activated cranial cervical cord neurons affect left ventricular infarct size and the potential for sudden cardiac death.

E Marie Southerland, David D Gibbons, S Brooks Smith, Adam Sipe, Carole Ann Williams, Eric Beaumont, J Andrew Armour, Robert D Foreman, Jeffrey L Ardell

Open access · greenAbstract read
In one paragraph

Article in Autonomic neuroscience : basic & clinical, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-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

14 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Autonomic Regulation Therapy in Heart Failure.Current heart failure reports · 2015
    Review
  12. Review
  13. Neural mechanisms of cardioprotection.Physiology (Bethesda, Md.) · 2014
    Review
  14. 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

9 authors at 3 institutions in 2 countries.

E Marie SoutherlandDepartment of Pharmacology, East Tennessee State University, Johnson City, TN, United States.
David D Gibbons
S Brooks Smith
Adam Sipe
Carole Ann Williams
Eric Beaumont
J Andrew Armour
Robert D Foreman
Jeffrey L Ardell
East Tennessee State University · USUniversité de Montréal · CAUniversity of Oklahoma Health Sciences Center · US

Funding

INTERDISCIPLINARY CARDIOVASCULAR RESEARCH FELLOWSHIPT32HL007121 · NHLBI · UNIVERSITY OF IOWA · PI LONDON, BARRY · 1985 to 2020
$15.1M
Myocardial Ischemia Remodels the Cardiac Nervous SystemR01HL071830 · NHLBI · EAST TENNESSEE STATE UNIVERSITY · PI ARDELL, JEFFREY L · 2005 to 2013
$2.8M
NHLBI NIH HHS HL71830NHLBI NIH HHS R01 HL071830NHLBI NIH HHS T32 HL007121
6 · The paper itself

Abstract

To evaluate whether cervical spinal neurons can influence cardiac indices and myocyte viability in the acutely ischemic heart, the hearts of anesthetized rabbits subjected to 30 min of LAD coronary arterial occlusion (CAO) were studied 3h after reperfusion. Control animals were compared to those exposed to pre-emptive high cervical cord stimulation (SCS; the dorsal aspect of the C1-C2 spinal cord was stimulated electrically at 50 Hz; 0.2 ms; 90% of motor threshold, starting 15 min prior to and continuing throughout CAO). Four groups of animals were so tested: 1) neuroaxis intact; 2) prior cervical vagotomy; 3) prior transection of the dorsal spinal columns at C6; and 4) following pharmacological treatment [muscarinic (atropine) or adrenergic (atenolol, prazosin or yohimbine) receptor blockade]. Infarct size (IS) was measured by tetrazolium, expressed as percentage of risk zone. C1-C2 SCS reduced acute ischemia induced IS by 43%, without changing the incidence of sudden cardiac death (SCD). While SCS-induced reduction in IS was unaffected by vagotomy, it was no longer evident following transection of C6 dorsal columns or atropinization. Beta-adrenoceptor blockade eliminated ischemia induced SCD, while alpha-receptor blockade doubled its incidence. During SCS, myocardial ischemia induced SCD was eliminated following vagotomy while remaining unaffected by atropinization. These data indicate that, in contrast to thoracic spinal neurons, i) cranial cervical spinal neurons affect both adrenergic and cholinergic motor outflows to the heart such that ii) their activation modifies ventricular infarct size and lethal arrhythmogenesis.

Indexed as

Electric Stimulation TherapyAdrenergic alpha-AntagonistsAdrenergic beta-AntagonistsAdrenergic NeuronsAnimalsCervical VertebraeCholinergic NeuronsCoronary OcclusionCranial NervesDeath, Sudden, CardiacDenervationDisease Models, AnimalFemaleHeart VentriclesMaleMyocardial InfarctionAdrenergic alpha-AntagonistsAdrenergic beta-Antagonists

Identifiers

PMID22502863
PMCPMC3361540
OpenAlexW2040154040

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.