Literature DB >> 34133239

Emerging cellular-based therapies in carbon monoxide poisoning.

David H Jang1,2, Sarah Piel2, John C Greenwood1, Johannes K Ehinger3,4, Todd J Kilbaugh2.   

Abstract

Carbon monoxide (CO) is an odorless and colorless gas with multiple sources that include engine exhaust, faulty furnaces, and other sources of incomplete combustion of carbon compounds such as house fires. The most serious complications for survivors of consequential CO exposure are persistent neurological sequelae occurring in up to 50% of patients. CO inhibits mitochondrial respiration by specifically binding to the heme a3 in the active site of CIV-like hydrogen sulfide, cyanide, and phosphides. Although hyperbaric oxygen remains the cornerstone for treatment, it has variable efficacy requiring new approaches to treatment. There is a paucity of cellular-based therapies in the area of CO poisoning, and there have been recent advancements that include antioxidants and a mitochondrial substrate prodrug. The succinate prodrugs derived from chemical modification of succinate are endeavored to enhance delivery of succinate to cells, increasing uptake of succinate into the mitochondria, and providing metabolic support for cells. The therapeutic intervention of succinate prodrugs is thus potentially applicable to patients with CO poisoning via metabolic support for fuel oxidation and possibly improving efficacy of HBO therapy.

Entities:  

Keywords:  carbon monoxide; cellular therapies; mitochondria; respiration; succinate prodrug

Mesh:

Substances:

Year:  2021        PMID: 34133239      PMCID: PMC8424679          DOI: 10.1152/ajpcell.00022.2021

Source DB:  PubMed          Journal:  Am J Physiol Cell Physiol        ISSN: 0363-6143            Impact factor:   5.282


  47 in total

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Journal:  J Biol Chem       Date:  1955-11       Impact factor: 5.157

2.  Respiratory enzymes in oxidative phosphorylation. V. A mechanism for oxidative phosphorylation.

Authors:  B CHANCE; G R WILLIAMS; W F HOLMES; J HIGGINS
Journal:  J Biol Chem       Date:  1955-11       Impact factor: 5.157

Review 3.  Carbon monoxide cardiotoxicity.

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4.  Mitochondrial dysfunction in peripheral blood mononuclear cells in pediatric septic shock.

Authors:  Scott L Weiss; Mary A Selak; Florin Tuluc; Jose Perales Villarroel; Vinay M Nadkarni; Clifford S Deutschman; Lance B Becker
Journal:  Pediatr Crit Care Med       Date:  2015-01       Impact factor: 3.624

Review 5.  Resveratrol and Brain Mitochondria: a Review.

Authors:  Fernanda Rafaela Jardim; Fernando Tonon de Rossi; Marielle Xavier Nascimento; Renata Gabriele da Silva Barros; Paula Agrizzi Borges; Isabella Cristina Prescilio; Marcos Roberto de Oliveira
Journal:  Mol Neurobiol       Date:  2017-03-10       Impact factor: 5.590

6.  Preclinical evaluation of injectable reduced hydroxocobalamin as an antidote to acute carbon monoxide poisoning.

Authors:  Joseph D Roderique; Christopher S Josef; Alden H Newcomb; Penny S Reynolds; Leonardo G Somera; Bruce D Spiess
Journal:  J Trauma Acute Care Surg       Date:  2015-10       Impact factor: 3.313

7.  Mitochondrial bioenergetics and structural network organization.

Authors:  Giovanni Benard; Nadège Bellance; Dominic James; Philippe Parrone; Helder Fernandez; Thierry Letellier; Rodrigue Rossignol
Journal:  J Cell Sci       Date:  2007-02-13       Impact factor: 5.285

Review 8.  Mitochondrial function in sepsis: respiratory versus leg muscle.

Authors:  Katarina Fredriksson; Olav Rooyackers
Journal:  Crit Care Med       Date:  2007-09       Impact factor: 7.598

Review 9.  Carbon Monoxide Poisoning: Pathogenesis, Management, and Future Directions of Therapy.

Authors:  Jason J Rose; Ling Wang; Qinzi Xu; Charles F McTiernan; Sruti Shiva; Jesus Tejero; Mark T Gladwin
Journal:  Am J Respir Crit Care Med       Date:  2017-03-01       Impact factor: 21.405

10.  Metformin induces lactate production in peripheral blood mononuclear cells and platelets through specific mitochondrial complex I inhibition.

Authors:  S Piel; J K Ehinger; E Elmér; M J Hansson
Journal:  Acta Physiol (Oxf)       Date:  2014-05-23       Impact factor: 6.311

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