Emerging cellular-based therapies in carbon monoxide poisoning

被引:4
|
作者
Jang, David H. [1 ,2 ]
Piel, Sarah [2 ]
Greenwood, John C. [1 ]
Ehinger, Johannes K. [3 ,4 ]
Kilbaugh, Todd J. [2 ]
机构
[1] Univ Penn, Perelman Sch Med, Dept Emergency Med, Philadelphia, PA 19104 USA
[2] Childrens Hosp Philadelphia, CHOP Res Inst, Resuscitat Sci Ctr, Dept Anesthesiol & Crit Care Med, Philadelphia, PA 19104 USA
[3] Lund Univ, Dept Clin Sci Lund, Mitochondrial Med, Lund, Sweden
[4] Skane Univ Hosp, Dept Otorhinolaryngol Head & Neck Surg, Lund, Sweden
来源
关键词
carbon monoxide; cellular therapies; mitochondria; respiration; succinate prodrug; BLOOD MONONUCLEAR-CELLS; MITOCHONDRIAL RESPIRATION; OXIDATIVE-PHOSPHORYLATION; ENDOTHELIAL-CELLS; ROS PRODUCTION; NITRIC-OXIDE; COMPLEX II; ENZYMES; MOTILITY; SEPSIS;
D O I
10.1152/ajpcell.00022.2021
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:C269 / C275
页数:7
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