{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,12]],"date-time":"2026-03-12T03:24:30Z","timestamp":1773285870588,"version":"3.50.1"},"reference-count":38,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"7","content-domain":{"domain":["www.ahajournals.org"],"crossmark-restriction":true},"short-container-title":["JAHA"],"published-print":{"date-parts":[[2016,7,6]]},"abstract":"<jats:sec xml:lang=\"en\">\n            <jats:title>Background<\/jats:title>\n            <jats:p xml:lang=\"en\">\n              We previously have shown that glibenclamide (\n              <jats:styled-content style=\"fixed-case\">GBC<\/jats:styled-content>\n              ), a sulfonylurea receptor 1\u2013transient receptor potential M4 (\n              <jats:styled-content style=\"fixed-case\">SUR<\/jats:styled-content>\n              1\u2010\n              <jats:styled-content style=\"fixed-case\">TRPM<\/jats:styled-content>\n              4) channel inhibitor, improves survival and neurological outcome after asphyxial cardiac arrest and cardiopulmonary resuscitation (\n              <jats:styled-content style=\"fixed-case\">ACA<\/jats:styled-content>\n              \/\n              <jats:styled-content style=\"fixed-case\">CPR<\/jats:styled-content>\n              ). Here, we further compare the efficacy of\n              <jats:styled-content style=\"fixed-case\">GBC<\/jats:styled-content>\n              with target temperature management (\n              <jats:styled-content style=\"fixed-case\">TTM<\/jats:styled-content>\n              ) and determine whether the efficacy of\n              <jats:styled-content style=\"fixed-case\">GBC<\/jats:styled-content>\n              is affected by\n              <jats:styled-content style=\"fixed-case\">TTM<\/jats:styled-content>\n              .\n            <\/jats:p>\n          <\/jats:sec>\n          <jats:sec xml:lang=\"en\">\n            <jats:title>Methods and Results<\/jats:title>\n            <jats:p xml:lang=\"en\">\n              Male Sprague\u2010Dawley rats (n=213) subjected to 10\u2010minute\n              <jats:styled-content style=\"fixed-case\">ACA<\/jats:styled-content>\n              \/\n              <jats:styled-content style=\"fixed-case\">CPR<\/jats:styled-content>\n              were randomized to 4 groups after return of spontaneous circulation (\n              <jats:styled-content style=\"fixed-case\">ROSC<\/jats:styled-content>\n              ): normothermia control (\n              <jats:styled-content style=\"fixed-case\">NT<\/jats:styled-content>\n              );\n              <jats:styled-content style=\"fixed-case\">GBC<\/jats:styled-content>\n              ;\n              <jats:styled-content style=\"fixed-case\">TTM<\/jats:styled-content>\n              ; and\n              <jats:styled-content style=\"fixed-case\">TTM<\/jats:styled-content>\n              +\n              <jats:styled-content style=\"fixed-case\">GBC<\/jats:styled-content>\n              . Survival, neurodeficit scores, histological injury, as well as the expressions of\n              <jats:styled-content style=\"fixed-case\">SUR<\/jats:styled-content>\n              1 and\n              <jats:styled-content style=\"fixed-case\">TRPM<\/jats:styled-content>\n              4 were evaluated. The 7\u2010day survival rate was 34.4% (11 of 32) in the\n              <jats:styled-content style=\"fixed-case\">NT<\/jats:styled-content>\n              group, 65% (13 of 20) in the\n              <jats:styled-content style=\"fixed-case\">GBC<\/jats:styled-content>\n              group, 50% (10 of 20) in the\n              <jats:styled-content style=\"fixed-case\">TTM<\/jats:styled-content>\n              group, and 70% (14 of 20) in the\n              <jats:styled-content style=\"fixed-case\">TTM<\/jats:styled-content>\n              +\n              <jats:styled-content style=\"fixed-case\">GBC<\/jats:styled-content>\n              group. Rats that received either\n              <jats:styled-content style=\"fixed-case\">GBC<\/jats:styled-content>\n              ,\n              <jats:styled-content style=\"fixed-case\">TTM<\/jats:styled-content>\n              alone, or in combination showed less neurological deficit than\n              <jats:styled-content style=\"fixed-case\">NT<\/jats:styled-content>\n              control at 24, 48, and 72\u00a0hours and 7\u00a0days after\n              <jats:styled-content style=\"fixed-case\">ROSC<\/jats:styled-content>\n              . Moreover,\n              <jats:styled-content style=\"fixed-case\">TTM<\/jats:styled-content>\n              or\n              <jats:styled-content style=\"fixed-case\">GBC<\/jats:styled-content>\n              ameliorated neuronal degeneration and glial activation in the hippocampal\n              <jats:styled-content style=\"fixed-case\">CA<\/jats:styled-content>\n              1 region with similar efficacy, whereas the combination of them had a trend toward better effect. The subunits of\n              <jats:styled-content style=\"fixed-case\">SUR<\/jats:styled-content>\n              1\u2010\n              <jats:styled-content style=\"fixed-case\">TRPM<\/jats:styled-content>\n              4 heterodimers were both strongly upregulated after\n              <jats:styled-content style=\"fixed-case\">ACA<\/jats:styled-content>\n              \/\n              <jats:styled-content style=\"fixed-case\">CPR<\/jats:styled-content>\n              and expressed in multiple types of brain cells, but partly suppressed by\n              <jats:styled-content style=\"fixed-case\">TTM<\/jats:styled-content>\n              .\n            <\/jats:p>\n          <\/jats:sec>\n          <jats:sec xml:lang=\"en\">\n            <jats:title>Conclusions<\/jats:title>\n            <jats:p xml:lang=\"en\">\n              <jats:styled-content style=\"fixed-case\">GBC<\/jats:styled-content>\n              is comparable to\n              <jats:styled-content style=\"fixed-case\">TTM<\/jats:styled-content>\n              in improving survival and neurological outcome after\n              <jats:styled-content style=\"fixed-case\">ACA<\/jats:styled-content>\n              \/\n              <jats:styled-content style=\"fixed-case\">CPR<\/jats:styled-content>\n              . When\n              <jats:styled-content style=\"fixed-case\">GBC<\/jats:styled-content>\n              is given along with\n              <jats:styled-content style=\"fixed-case\">TTM<\/jats:styled-content>\n              , less histological injury tended to be achieved.\n            <\/jats:p>\n          <\/jats:sec>","DOI":"10.1161\/jaha.116.003465","type":"journal-article","created":{"date-parts":[[2016,7,14]],"date-time":"2016-07-14T05:57:19Z","timestamp":1468475839000},"update-policy":"https:\/\/doi.org\/10.1161\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":32,"title":["Glibenclamide Is Comparable to Target Temperature Management in Improving Survival and Neurological Outcome After Asphyxial Cardiac Arrest in Rats"],"prefix":"10.1161","volume":"5","author":[{"given":"Kaibin","family":"Huang","sequence":"first","affiliation":[{"name":"Department of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, 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