{"title":"氰化物中毒诱导兔心肌肾上腺素释放","authors":"Toru Kawada , Toji Yamazaki , Tsuyoshi Akiyama , Takayuki Sato , Toshiaki Shishido , Masashi Inagaki , Teiji Tatewaki , Yusuke Yanagiya , Masaru Sugimachi , Kenji Sunagawa","doi":"10.1016/S0165-1838(00)00086-2","DOIUrl":null,"url":null,"abstract":"<div><p>Cyanide intoxication, which has been used as a model of energy depletion at cardiac sympathetic nerve terminals, causes non-exocytotic release of norepinephrine (NE). However, the effect of cyanide intoxication on cardiac epinephrine (Epi) release remains unknown. Using cardiac microdialysis in the rabbit, we measured dialysate Epi and NE concentrations as indices of myocardial interstitial Epi and NE levels, respectively. Local administration of sodium cyanide (30 mM) through the dialysis probe increased both Epi and NE levels (from 11.3±2.3 to 32.3±4.4 pg/ml and from 33.6±6.1 to 389.0±71.8 pg/ml, respectively, mean±S.E., <em>P</em><0.01). Local desipramine (100 μM) administration suppressed the cyanide induced NE response without affecting the Epi response. In contrast, local ω-conotoxin GVIA (10 μM) administration partially suppressed the cyanide induced NE response and totally abolished the Epi response. In conclusion, cyanide intoxication causes N-type Ca<sup>2+</sup> channel dependent exocytotic Epi release as well as inducing N-type Ca<sup>2+</sup> channel independent non-exocytotic NE release.</p></div>","PeriodicalId":17228,"journal":{"name":"Journal of the autonomic nervous system","volume":"80 3","pages":"Pages 137-141"},"PeriodicalIF":0.0000,"publicationDate":"2000-05-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0165-1838(00)00086-2","citationCount":"8","resultStr":"{\"title\":\"Cyanide intoxication induced exocytotic epinephrine release in rabbit myocardium\",\"authors\":\"Toru Kawada , Toji Yamazaki , Tsuyoshi Akiyama , Takayuki Sato , Toshiaki Shishido , Masashi Inagaki , Teiji Tatewaki , Yusuke Yanagiya , Masaru Sugimachi , Kenji Sunagawa\",\"doi\":\"10.1016/S0165-1838(00)00086-2\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Cyanide intoxication, which has been used as a model of energy depletion at cardiac sympathetic nerve terminals, causes non-exocytotic release of norepinephrine (NE). However, the effect of cyanide intoxication on cardiac epinephrine (Epi) release remains unknown. Using cardiac microdialysis in the rabbit, we measured dialysate Epi and NE concentrations as indices of myocardial interstitial Epi and NE levels, respectively. Local administration of sodium cyanide (30 mM) through the dialysis probe increased both Epi and NE levels (from 11.3±2.3 to 32.3±4.4 pg/ml and from 33.6±6.1 to 389.0±71.8 pg/ml, respectively, mean±S.E., <em>P</em><0.01). Local desipramine (100 μM) administration suppressed the cyanide induced NE response without affecting the Epi response. In contrast, local ω-conotoxin GVIA (10 μM) administration partially suppressed the cyanide induced NE response and totally abolished the Epi response. In conclusion, cyanide intoxication causes N-type Ca<sup>2+</sup> channel dependent exocytotic Epi release as well as inducing N-type Ca<sup>2+</sup> channel independent non-exocytotic NE release.</p></div>\",\"PeriodicalId\":17228,\"journal\":{\"name\":\"Journal of the autonomic nervous system\",\"volume\":\"80 3\",\"pages\":\"Pages 137-141\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2000-05-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/S0165-1838(00)00086-2\",\"citationCount\":\"8\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of the autonomic nervous system\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0165183800000862\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the autonomic nervous system","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0165183800000862","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Cyanide intoxication induced exocytotic epinephrine release in rabbit myocardium
Cyanide intoxication, which has been used as a model of energy depletion at cardiac sympathetic nerve terminals, causes non-exocytotic release of norepinephrine (NE). However, the effect of cyanide intoxication on cardiac epinephrine (Epi) release remains unknown. Using cardiac microdialysis in the rabbit, we measured dialysate Epi and NE concentrations as indices of myocardial interstitial Epi and NE levels, respectively. Local administration of sodium cyanide (30 mM) through the dialysis probe increased both Epi and NE levels (from 11.3±2.3 to 32.3±4.4 pg/ml and from 33.6±6.1 to 389.0±71.8 pg/ml, respectively, mean±S.E., P<0.01). Local desipramine (100 μM) administration suppressed the cyanide induced NE response without affecting the Epi response. In contrast, local ω-conotoxin GVIA (10 μM) administration partially suppressed the cyanide induced NE response and totally abolished the Epi response. In conclusion, cyanide intoxication causes N-type Ca2+ channel dependent exocytotic Epi release as well as inducing N-type Ca2+ channel independent non-exocytotic NE release.