Evidence map›Paper›PMID 19513821›Full record

ReviewJournal of bioenergetics and biomembranes2009

Mitochondrial matters of the heart: a plethora of regulatory modes to maintain function for a long lifetime.

Peter L Pedersen

Abstract readReview
PubMed Publisher
In one paragraph

Review in Journal of bioenergetics and biomembranes, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
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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

1 author at 1 institution in 1 country.

Peter L PedersenDepartment of Biological Chemistry, School of Medicine, Johns Hopkins University, 725 North Wolfe Street, Baltimore, MD 21205-2185, USA. ppederse@jhmi.edu
Johns Hopkins Medicine · US

Funding

STRUCTURE OF MITOCHONDRIAL K+ CHANNELSP01HL081427 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI VAN EYK, JENNIFER E · 2005 to 2009
$11.2M
CONTROL OF ENZYMATIC PHOSPHATE TRANSFER IN MITOCHONDRIAR01CA010951 · NCI · JOHNS HOPKINS UNIVERSITY · PI PEDERSEN, PETER L · 1985 to 2009
$3.7M
CANCER-RELATED GLYCOLYTIC GENE--REGULATION/TARGETINGR01CA080118 · NCI · JOHNS HOPKINS UNIVERSITY · PI PEDERSEN, PETER L · 1999 to 2008
$2.2M
NCI NIH HHS 2R01CA080118NCI NIH HHS 5R01CA10951NHLBI NIH HHS 5P01HL081427
6 · The paper itself

Abstract

The human/animal heart, comprised of cells called "myocytes" is an incredible organ that to remain beating must be fueled constantly via the hydrolysis of adenosine tri-phosphate (ATP). Deriving most of its ATP from mitochondrial oxidative phosphorylation (ox phos), and a smaller amount from "glycolysis", i.e., glucose conversion to pyruvate or lactate, the heart helps in the delivery of oxygen (via hemoglobin) to every organ/tissue in our body. Then, the empty (deoxy) hemoglobin returns to load more oxygen and the journey to tissues is repeated 24 h a day, year after year, until "death do us part". To support this essential "pumping" process the heart must work constantly, i.e., 70-80 years (life expectancy in the U.S.). This is a remarkable feat when compared with one of our most costly people-made technologies, i.e., automobiles (cars). In the past century, it was rare to see the family car survive more than 10-15 years unless it had been subjected to motor replacement surgery. Most were laid to rest at a much earlier age. Now, in this new millennium should a brilliant car manufacturer succeed in constructing a car engine as efficient as the human heart, each family member requiring a car would need only one per life time. With this in mind, one of the major future "matters of the heart" is to keep it pumping, not only for the current 70-80 year life span but much longer. To do this depends on, among other matters, the two processes noted above, i.e., oxidative phosphorylation and glycolysis. The former is strictly a mitochondrial process that works only in the presence of oxygen whereas glycolysis, dependent on mitochondrial bound hexokinase 2 (MB-HK-2), works either in the presence or absence of oxygen. In addition, the MB-HK 2 is anti-apoptotic and helps with other factors to retard cell death. Current estimates reveal that the human heart of an individual living 70-80 years will have undergone 2.5-3.0 billion beats, a feat that is energetically feasible only due to the heart cells' (cardiomyocytes) large population of mitochondria with bound HK-2.

Indexed as

Oxidative PhosphorylationAdenosine TriphosphateAnimalsGlucoseGlycolysisHexokinaseHumansLactic AcidLongevityMitochondria, HeartMitochondrial MembranesPyruvic AcidAdenosine TriphosphateGlucoseHexokinaseLactic AcidPyruvic Acid

Identifiers

PMID19513821
OpenAlexW1973862435

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.