Evidence map›Paper›PMID 27241357›Full record

ArticleJournal of cellular and molecular medicine2016

Heat shock protein 70 and AMP-activated protein kinase contribute to 17-DMAG-dependent protection against heat stroke.

Yung-Chieh Tsai, Kwok-Keung Lam, Yi-Jen Peng, Yen-Mei Lee, Chung-Yu Yang, Yi-Ju Tsai, Mao-Hsiung Yen, Pao-Yun Cheng

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

18 citing papers in PubMed, 34 citations in OpenAlex.

  1. Trial
  2. Review
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  5. Review
  6. Article
  7. Microglia polarization in heat-induced early neural injury.Archives of medical science : AMS · 2024
    Article
  8. Article
  9. Article
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  11. Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Heat stroke.Journal of intensive care · 2018
    Review
  18. 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

8 authors at 4 institutions in 1 country.

Yung-Chieh TsaiDepartment of Obstetrics and Gynecology, Chi-Mei Medical Center, Tainan, Taiwan.
Kwok-Keung LamDepartment of Pharmacology, Taipei Medical University, Taipei, Taiwan.
Yi-Jen PengDepartment of Pathology, Tri-Service General Hospital and National Defense Medical Center, Taipei, Taiwan.
Yen-Mei LeeDepartment of Pharmacology, National Defense Medical Center, Taipei, Taiwan.
Chung-Yu YangDepartment of Pharmacology, National Defense Medical Center, Taipei, Taiwan.
Yi-Ju TsaiDepartment of Pharmacology, National Defense Medical Center, Taipei, Taiwan.
Mao-Hsiung YenDepartment of Pharmacology, National Defense Medical Center, Taipei, Taiwan.
Pao-Yun ChengDepartment of Physiology and Biophysics, National Defense Medical Center, Taipei, Taiwan. pycheng@mail.ndmctsgh.edu.tw.
National Defense Medical Center · TWChia Nan University of Pharmacy and Science · TWChi Mei Medical Center · TWTaipei Medical University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heat shock protein 70 (Hsp70) preconditioning induces thermotolerance, and adenosine monophosphate (AMP)-activated protein kinase (AMPK) plays a role in the process of autophagy. Here, we investigated whether 17-dimethylaminoethylamino-17-demethoxy-geldanamycin (17-DMAG) protected against heat stroke (HS) in rats by up-regulation of Hsp70 and phosphorylated AMPK (pAMPK). To produce HS, male Sprague-Dawley rats were placed in a chamber with an ambient temperature of 42°C. Physiological function (mean arterial pressure, heart rate and core temperature), hepatic and intestinal injury, inflammatory mediators and levels of Hsp70, pAMPK and light chain 3 (LC3B) in hepatic tissue were measured in HS rats or/and rats pre-treated with 17-DMAG. 17-DMAG pre-treatment significantly attenuated hypotension and organ dysfunction induced by HS in rats. The survival time during HS was also prolonged by 17-DMAG treatment. Hsp70 expression was increased, whereas pAMPK levels in the liver were significantly decreased in HS rats. Following pre-treatment with 17-DMAG, Hsp70 protein levels increased further, and pAMPK levels were enhanced. Treatment with an AMPK activator significantly increased the LC3BII/LC3BI ratio as a marker of autophagy in HS rats. Treatment with quercetin significantly suppressed Hsp70 and pAMPK levels and reduced the protective effects of 17-DMAG in HS rats. Both of Hsp70 and AMPK are involved in the 17-DMAG-mediated protection against HS. 17-DMAG may be a promising candidate drug in the clinical setting.

Indexed as

AMP-Activated Protein KinasesAnimalsAutophagyBenzoquinonesDNA-Binding ProteinsHeat Shock Transcription FactorsHeat StrokeHSP70 Heat-Shock ProteinsIleumInflammation MediatorsLactams, MacrocyclicMalePhosphorylationProtective AgentsRats, Sprague-DawleySurvival Analysis17-(dimethylaminoethylamino)-17-demethoxygeldanamycinAMP-Activated Protein KinasesBenzoquinonesDNA-Binding ProteinsHeat Shock Transcription FactorsHSP70 Heat-Shock ProteinsInflammation MediatorsLactams, MacrocyclicProtective AgentsTranscription Factors17-DMAGAMP-activated protein kinaseautophagyheat shock protein 70heat strokemortality

Identifiers

PMID27241357
PMCPMC5020632
OpenAlexW2412147418

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.