Evidence map›Paper›PMID 18006466›Full record

ArticleCardiovascular research2008

Human thrombopoietin reduces myocardial infarct size, apoptosis, and stunning following ischaemia/reperfusion in rats.

John E Baker, Jidong Su, Anna Hsu, Yang Shi, Ming Zhao, Jennifer L Strande, Xiangping Fu, Hao Xu, Annie Eis, Richard Komorowski and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Cardiovascular research, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

19 citing papers in PubMed, 47 citations in OpenAlex.

  1. SALVE: prediction of interorgan communication with transcriptome latent space representation.American journal of physiology. Heart and circulatory physiology · 2025
    Article
  2. Review
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  6. [Thrombopoietin promotes megakaryopoiesisNan fang yi ke da xue xue bao = Journal of Southern Medical University · 2020
    Article
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  14. Review
  15. Intestinal microbiota determine severity of myocardial infarction in rats.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2012
    Article
  16. Review
  17. Thrombopoietin protects the brain and improves sensorimotor functions: reduction of stroke-induced MMP-9 upregulation and blood-brain barrier injury.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2011
    Article
  18. Article
  19. JAK redux: a second look at the regulation and role of JAKs in the heart.American journal of physiology. Heart and circulatory physiology · 2009
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 2 institutions in 1 country.

John E BakerDivision of Cardiothoracic Surgery, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI 53226, USA. jbaker@mcw.edu
Jidong Su
Anna Hsu
Yang Shi
Ming Zhao
Jennifer L Strande
Xiangping Fu
Hao Xu
Annie Eis
Richard Komorowski
Eric S Jensen
James S Tweddell
Parvaneh Rafiee
Garrett J Gross
Medical College of Wisconsin · USBoston Children's Hospital · US

Funding

EFFECTS OF DRUGS UPON MYOCARDIAL HYPOXIAR01HL008311 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI GROSS, GARRETT JOHN · 1985 to 2009
$2.7M
NITRIC OXIDE AND TOLERANCE OF HYPOXIC HEART TO ISCHEMIAR01HL054075 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI BAKER, JOHN E · 1997 to 2010
$2.5M
NHLBI NIH HHS HL 08311NHLBI NIH HHS HL 54075NHLBI NIH HHS R01 HL008311NHLBI NIH HHS R01 HL054075
6 · The paper itself

Abstract

aimsThrombopoietin (Tpo) is known for its ability to stimulate platelet production. However, it is currently unknown whether Tpo plays a physiological function in the heart. METHODS AND

resultsWe assessed the potential protective role of Tpo in vitro and in vivo in two rat models of myocardial ischaemia/reperfusion. Tpo receptor (c-mpl) message was detected in the heart using RT-PCR, and the Tpo receptor protein was detected using western blotting and immunohistochemistry. Tpo treatment immediately before ischaemia reduced myocardial necrosis, apoptosis, and decline in ventricular function following ischaemia/reperfusion in the rat in a concentration- and dose-dependent manner with an optimal concentration of 1.0 ng/mL in vitro and an optimal dose of 0.05 microg/kg iv in vivo. Tpo also reduced infarct size when given after the onset of ischaemia or at reperfusion. Tpo activated JAK-2 (Janus kinase-2) and p44 MAPK (mitogen-activated protein kinase) during reperfusion but not prior to ischaemia. Inhibition of JAK-2 (AG-490), p42/44 MAPK (PD98059), mitochondrial K(ATP) channels (5-HD), and sarcolemmal K(ATP) channels (HMR 1098) abolished Tpo-induced resistance to injury from myocardial ischaemia/reperfusion. AG-490, PD98059, 5-HD, and HMR1098 alone had no effect on cardioprotection. Treatment with a single dose of Tpo (0.05 or 1.0 microg/kg iv) did not result in the elevation of platelet count or haematocrit over a 16-day period.

conclusionA single treatment of Tpo confers cardioprotection through JAK-2, p42/44 MAPK, and K(ATP) channels, suggesting a potential therapeutic role of Tpo in the treatment of injury resulting from myocardial ischaemia and reperfusion.

Indexed as

AnimalsApoptosisExtracellular Signal-Regulated MAP KinasesHumansIn Vitro TechniquesJanus Kinase 2KATP ChannelsMaleMyocardial InfarctionMyocardial Reperfusion InjuryMyocardial StunningRatsRats, Sprague-DawleySTAT3 Transcription FactorThrombopoietinTime FactorsExtracellular Signal-Regulated MAP KinasesJak2 protein, ratJanus Kinase 2KATP ChannelsStat3 protein, ratSTAT3 Transcription FactorThrombopoietin

Identifiers

PMID18006466
PMCPMC2958050
OpenAlexW2119159562

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.