Evidence map›Paper›PMID 18430807›Full record

ArticlePhysiological genomics2008

Physiological and molecular evidence of heat acclimation memory: a lesson from thermal responses and ischemic cross-tolerance in the heart.

Anna Tetievsky, Omer Cohen, Luba Eli-Berchoer, Gary Gerstenblith, Michael D Stern, Ilan Wapinski, Nir Friedman, Michal Horowitz

Open access · greenAbstract read
In one paragraph

Article in Physiological genomics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 14% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 58 citations in OpenAlex.

  1. Pooled it
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  11. Long-term HIF-1α transcriptional activation is essential for heat-acclimation-mediated cross tolerance: mitochondrial target genes.American journal of physiology. Regulatory, integrative and comparative physiology · 2017
    Article
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  19. Regulation of survival gene hsp70.Cell stress & chaperones · 2012
    Review
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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

8 authors at 3 institutions in 2 countries.

Anna TetievskyLaboratory of Environmental Physiology, Faculty of Dental Medicine, The Hebrew University, Jerusalem, Israel.
Omer Cohen
Luba Eli-Berchoer
Gary Gerstenblith
Michael D Stern
Ilan Wapinski
Nir Friedman
Michal Horowitz
Hebrew University of Jerusalem · ILJohns Hopkins Medicine · USNational Institute on Aging · US

Funding

Stochastic Simulation Of Excitation-contraction CouplingZIAAG000844 · NIA · NATIONAL INSTITUTE ON AGING · PI STERN, MICHAEL · 2009 to 2025
$8.7M
STOCHASTIC SIMULATION OF EXCITATION-CONTRACTION COUPLINGZ01AG000844 · NIA · NATIONAL INSTITUTE ON AGING · PI STERN, MICHAEL D · 1997 to 2008
$1.1M
Intramural NIH HHS Z01 AG000844Intramural NIH HHS ZIA AG000844
6 · The paper itself

Abstract

Sporadic findings in humans suggest that reinduction of heat acclimation (AC) after its loss occurs markedly faster than that during the initial AC session. Animal studies substantiated that the underlying acclimatory processes are molecular. Here we test the hypothesis that faster reinduction of AC (ReAC) implicates "molecular memory." In vivo measurements of colonic temperature profiles during heat stress and ex vivo assessment of cross-tolerance to ischemia-reperfusion or anoxia insults in the heart demonstrated that ReAC only needs 2 days vs. the 30 days required for the initial development of AC. Stress gene profiling in the experimental groups highlighted clusters of transcriptionally activated genes (37%), which included heat shock protein (HSP) genes, antiapoptotic genes, and chromatin remodeling genes. Despite a return of the physiological phenotype to its preacclimation state, after a 1 mo deacclimation (DeAC) period, the gene transcripts did not resume their preacclimation levels, suggesting a dichotomy between genotype and phenotype in this system. Individual detection of hsp70 and hsf1 transcripts agreed with these findings. HSP72, HSF1/P-HSF1, and Bcl-xL protein profiles followed the observed dichotomized genomic response. In contrast, HSP90, an essential cytoprotective component mismatched transcriptional activation upon DeAC. The uniform activation of the similarly responding gene clusters upon De-/ReAC implies that reacclimatory phenotypic plasticity is associated with upstream denominators. During AC, DeAC, and ReAC, the maintenance of elevated/phosphorylated HSF1 protein levels and transcriptionally active chromatin remodeling genes implies that chromatin remodeling plays a pivotal role in the transcriptome profile and in preconditioning to rapid cytoprotective acclimatory memory.

Indexed as

Heat-Shock ResponseHot TemperatureAcclimatizationAnimalsbcl-X ProteinDNA-Binding ProteinsGene Expression RegulationGenotypeHeartHeart VentriclesHeat-Shock ProteinsHeat Shock Transcription FactorsMaleMemoryMyocardial InfarctionMyocardial Ischemiabcl-X ProteinDNA-Binding ProteinsHeat-Shock ProteinsHeat Shock Transcription FactorsHSF1 protein, humanHsf1 protein, ratTranscription Factors

Identifiers

PMID18430807
PMCPMC10585612
OpenAlexW2035612080

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.