Evidence map›Paper›PMID 28572638›Full record

ArticleScientific reports2017

Mitochondrial targeting by dichloroacetate improves outcome following hemorrhagic shock.

Kumar Subramani, Sumin Lu, Marie Warren, Xiaogang Chu, Haroldo A Toque, R William Caldwell, Michael P Diamond, Raghavan Raju

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. 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
1.0field-weighted citation impact, top 25% 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, 23 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Mitochondria and sensory processing in inflammatory and neuropathic pain.Frontiers in pain research (Lausanne, Switzerland) · 2022
    Review
  8. Article
  9. Pharmacokinetic and Biochemical Profiling of Sodium Dichloroacetate in Pregnant Ewes and Fetuses.Drug metabolism and disposition: the biological fate of chemicals · 2020
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Mitochondrial dysfunction in rat splenocytes following hemorrhagic shock.Biochimica et biophysica acta. Molecular basis of disease · 2017
    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 1 institution in 1 country.

Kumar SubramaniDepartment of Laboratory Sciences, Augusta University, Augusta, GA, 30912, United States of America.
Sumin LuDepartment of Laboratory Sciences, Augusta University, Augusta, GA, 30912, United States of America.
Marie WarrenDepartment of Laboratory Sciences, Augusta University, Augusta, GA, 30912, United States of America.
Xiaogang ChuDepartment of Laboratory Sciences, Augusta University, Augusta, GA, 30912, United States of America.
Haroldo A ToqueDepartment of Pharmacology and Toxicology, Augusta University, Augusta, GA, 30912, United States of America.
R William CaldwellDepartment of Pharmacology and Toxicology, Augusta University, Augusta, GA, 30912, United States of America.
Michael P DiamondDepartment of Obstetrics and Gynaecology, Augusta University, Augusta, GA, 30912, United States of America.
Raghavan RajuDepartment of Laboratory Sciences, Augusta University, Augusta, GA, 30912, United States of America. RRaju@augusta.edu.
Augusta University · US

Funding

Resveratrol as an adjunct to resuscitation fluid following hemorrhage injuryR01GM101927 · NIGMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI RAJU, RAGHAVAN PILLAI · 2012 to 2016
$1.1M
NIGMS NIH HHS R01 GM101927
6 · The paper itself

Abstract

Hemorrhagic shock is a leading cause of death in people under the age of 45 and accounts for almost half of trauma-related deaths. In order to develop a treatment strategy based on potentiating mitochondrial function, we investigated the effect of the orphan drug dichloroacetate (DCA) on survival in an animal model of hemorrhagic shock in the absence of fluid resuscitation. Hemorrhagic shock was induced in rats by withdrawing 60% of the blood volume and maintaining a hypotensive state. The studies demonstrated prolonged survival of rats subjected to hemorrhagic injury (HI) when treated with DCA. In separate experiments, using a fluid resuscitation model we studied mitochondrial functional alterations and changes in metabolic networks connected to mitochondria following HI and treatment with DCA. DCA treatment restored cardiac mitochondrial membrane potential and tissue ATP in the rats following HI. Treatment with DCA resulted in normalization of several metabolic and molecular parameters including plasma lactate and p-AMPK/AMPK, as well as Ach-mediated vascular relaxation. In conclusion we demonstrate that DCA can be successfully used in the treatment of hemorrhagic shock in the absence of fluid resuscitation; therefore DCA may be a good candidate in prolonged field care following severe blood loss.

Indexed as

AnimalsChloroacetatesDose-Response Relationship, DrugKaplan-Meier EstimateMaleMembrane Potential, MitochondrialMitochondriaOrphan Drug ProductionRats, Sprague-DawleyShock, HemorrhagicChloroacetates

Identifiers

PMID28572638
PMCPMC5453974
OpenAlexW2617538983

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.