氰化物中毒诱导兔心肌肾上腺素释放

Toru Kawada , Toji Yamazaki , Tsuyoshi Akiyama , Takayuki Sato , Toshiaki Shishido , Masashi Inagaki , Teiji Tatewaki , Yusuke Yanagiya , Masaru Sugimachi , Kenji Sunagawa
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引用次数: 8

摘要

氰化物中毒,已被用作心脏交感神经末梢能量消耗的模型,引起去甲肾上腺素(NE)的非胞外释放。然而,氰化物中毒对心脏肾上腺素(Epi)释放的影响尚不清楚。通过兔心脏微透析,我们分别测定了透析液Epi和NE浓度作为心肌间质Epi和NE水平的指标。通过透析探头局部给药氰化钠(30mm)可使Epi和NE水平升高(分别从11.3±2.3至32.3±4.4 pg/ml和33.6±6.1至389.0±71.8 pg/ml,平均值±S.E.)术中,0.01)。局部给药地西帕明(100 μM)抑制了氰化物诱导的NE反应,但不影响Epi反应。相反,局部ω- concontoxin GVIA (10 μM)可部分抑制氰化物诱导的NE反应,完全消除Epi反应。综上所述,氰化物中毒引起n型Ca2+通道依赖性胞外Epi释放,并诱导n型Ca2+通道依赖性非胞外NE释放。
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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.

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