{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,15]],"date-time":"2026-03-15T22:16:40Z","timestamp":1773613000109,"version":"3.50.1"},"reference-count":74,"publisher":"Oxford University Press (OUP)","issue":"2","license":[{"start":{"date-parts":[[2021,7,16]],"date-time":"2021-07-16T00:00:00Z","timestamp":1626393600000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/journals\/pages\/open_access\/funder_policies\/chorus\/standard_publication_model"}],"funder":[{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","award":["R21NS116671"],"award-info":[{"award-number":["R21NS116671"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2021,9,28]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:p>Exposure to hydrogen sulfide (H2S) can cause neurotoxicity and cardiopulmonary arrest. Resuscitating victims of sulfide intoxication is extremely difficult, and survivors often exhibit persistent neurological deficits. However, no specific antidote is available for sulfide intoxication. The objective of this study was to examine whether administration of a sulfonyl azide-based sulfide-specific scavenger, SS20, would rescue mice in models of H2S intoxication: ongoing exposure and post-cardiopulmonary arrest. In the ongoing exposure model, SS20 (1250\u2009\u00b5mol\/kg) or vehicle was administered to awake CD-1 mice intraperitoneally at 10\u2009min after breathing 790\u2009ppm of H2S followed by another 30\u2009min of H2S inhalation. Effects of SS20 on survival were assessed. In the post-cardiopulmonary arrest model, cardiopulmonary arrest was induced by an intraperitoneal administration of sodium sulfide nonahydrate (125\u2009mg\/kg) in anesthetized mice. After 1\u2009min of cardiopulmonary arrest, mice were resuscitated with intravenous administration of SS20 (250\u2009\u00b5mol\/kg) or vehicle. Effects of SS20 on survival, neurological outcomes, and plasma H2S levels were evaluated. Administration of SS20 during ongoing H2S inhalation improved 24-h survival (6\/6 [100%] in SS20 vs 1\/6 [17%] in vehicle; p\u2009=\u2009.0043). Post-arrest administration of SS20 improved 7-day survival (4\/10 [40%] in SS20 vs 0\/10 [0%] in vehicle; p\u2009=\u2009.0038) and neurological outcomes after resuscitation. SS20 decreased plasma H2S levels to pre-arrest baseline immediately after reperfusion and shortened the time to return of spontaneous circulation and respiration. These results suggest that SS20 is an effective antidote against lethal H2S intoxication, even when administered after cardiopulmonary arrest.<\/jats:p>","DOI":"10.1093\/toxsci\/kfab088","type":"journal-article","created":{"date-parts":[[2021,7,15]],"date-time":"2021-07-15T19:11:31Z","timestamp":1626376291000},"page":"393-403","source":"Crossref","is-referenced-by-count":14,"title":["A Sulfonyl Azide-Based Sulfide Scavenger Rescues Mice from Lethal Hydrogen Sulfide Intoxication"],"prefix":"10.1093","volume":"183","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-7210-8609","authenticated-orcid":false,"given":"Yusuke","family":"Miyazaki","sequence":"first","affiliation":[{"name":"Department of Anesthesia, Critical Care and Pain Medicine, Anesthesia Center for Critical Care Research, Massachusetts General Hospital, Boston, Massachusetts, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Eizo","family":"Marutani","sequence":"additional","affiliation":[{"name":"Department of Anesthesia, Critical Care and Pain Medicine, Anesthesia Center for Critical Care Research, Massachusetts General Hospital, Boston, Massachusetts, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-1245-2958","authenticated-orcid":false,"given":"Takamitsu","family":"Ikeda","sequence":"additional","affiliation":[{"name":"Department of Anesthesia, Critical Care and Pain Medicine, Anesthesia Center for Critical Care Research, Massachusetts General Hospital, Boston, Massachusetts, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Xiang","family":"Ni","sequence":"additional","affiliation":[{"name":"Department of Chemistry, Brown University, Providence, Rhode Island"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kenjiro","family":"Hanaoka","sequence":"additional","affiliation":[{"name":"Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ming","family":"Xian","sequence":"additional","affiliation":[{"name":"Department of Chemistry, Brown University, Providence, Rhode Island"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Fumito","family":"Ichinose","sequence":"additional","affiliation":[{"name":"Department of Anesthesia, Critical Care and Pain Medicine, Anesthesia Center for Critical Care Research, Massachusetts General Hospital, Boston, Massachusetts, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"286","published-online":{"date-parts":[[2021,7,16]]},"reference":[{"key":"2021092818421075700_kfab088-B1","doi-asserted-by":"crossref","first-page":"12","DOI":"10.1007\/s11095-019-2745-x","article-title":"Intraperitoneal route of drug administration: Should it be used in experimental animal studies?","volume":"37","author":"Al Shoyaib","year":"2019","journal-title":"Pharm. 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