Ozutsumi K, Sugimoto N, Matsuda M
Biochem Biophys Res Commun. 1987 Apr 14;144(1):217-23. doi: 10.1016/s0006-291x(87)80498-9.
Clostridium perfringens type A enterotoxin(500 ng/ml) induced extensive release of noradrenaline (1/3-2/3 of the total cell content) from PC12 cells in 2-4 min in the presence, but not the absence of extracellular Ca2+. Cells treated with toxin in the absence of Ca2+ released noradrenaline promptly on subsequent addition of Ca2+ to the medium. The amount of noradrenaline released depended on the concentrations of both Ca2+ and toxin in the medium (ED50, 0.3 mM and 420 ng/ml respectively). Ca2+ could be replaced by Ba2+ or Sr2+, and Mn2+ or Co2+, which are Ca2+ channel blockers, did not inhibit the release of the transmitter. These findings are discussed in relation to the systemic effects of enterotoxin.
A型产气荚膜梭菌肠毒素(500纳克/毫升)在有细胞外钙离子存在但无细胞外钙离子不存在的情况下,于2至4分钟内诱导PC12细胞大量释放去甲肾上腺素(占细胞总含量的1/3 - 2/3)。在无钙离子的情况下用毒素处理的细胞,在随后向培养基中添加钙离子时会迅速释放去甲肾上腺素。去甲肾上腺素的释放量取决于培养基中钙离子和毒素的浓度(半数有效浓度分别为0.3毫摩尔和420纳克/毫升)。钙离子可用钡离子或锶离子替代,而作为钙离子通道阻滞剂的锰离子或钴离子并不抑制递质的释放。结合肠毒素的全身效应讨论了这些发现。