Cobinamide is effective for treatment of hydrogen sulfide–induced neurological sequelae in a mouse model. Issue 1 (14th December 2017)

• Record Type: Journal Article
• Authors: Anantharam, Poojya; Whitley, Elizabeth M.; Mahama, Belinda; Kim, Dong‐Suk; Sarkar, Souvarish; Santana, Cristina; Chan, Adriano; Kanthasamy, Anumantha G.; Kanthasamy, Arthi; Boss, Gerry R.; Rumbeiha, Wilson K.
• Is Part Of: Annals of the New York Academy of Sciences. Volume 1408:Issue 1(2017)
• Page Start: 61
• Page End: 78
• Publication Date: 2017-12-14
• Subjects: cobinamide -- hydrogen sulfide -- neurological sequelae -- neuroprotection; Medical sciences -- Periodicals; Medicine -- Periodicals; Science -- Periodicals; 610
• DOI: 10.1111/nyas.13559
• Languages: English
• ISSNs: 0077-8923

Abstract

Abstract: Hydrogen sulfide (H2 S) is a highly neurotoxic gas. Acute exposure can lead to neurological sequelae among survivors. A drug for treating neurological sequelae in survivors of acute H2 S intoxication is needed. Using a novel mouse model we evaluated the efficacy of cobinamide (Cob) for increasing survival of, and reducing neurological sequalae in, mice exposed to sublethal doses of H2 S. There were two objectives: (1) to determine the dose–response efficacy of Cob and (2) to determine the effective therapeutic time window of Cob. To explore objective 1, mice were injected intramuscularly with Cob at 0, 50, or 100 mg/kg at 2 min after H2 S exposure. For objective 2, mice were injected intramuscularly with 100 mg/kg Cob at 2, 15, and 30 min after H2 S exposure. For both objectives, mice were exposed to 765 ppm of H2 S gas. Cob significantly reduced H2 S‐induced lethality in a dose‐dependent manner ( P < 0.05). Cob‐treated mice exhibited significantly fewer seizures and knockdowns compared with the H2 S‐exposed group. Cob also reversed H2 S‐induced weight loss, behavioral deficits, neurochemical changes, cytochrome c oxidase enzyme inhibition, and neurodegeneration in a dose‐ and time‐dependent manner ( P < 0.01). Overall, these findings show that Cob increases survival and is neuroprotective in a mouse model of H2 S‐induced neurological sequelae.