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刺尾鱼毒素对昆虫骨骼肌钙通道的强大兴奋作用。

Potent excitatory effect of maitotoxin on Ca channels in the insect skeletal muscle.

作者信息

Miyamoto T, Ohizumi Y, Washio H, Yasumoto Y

出版信息

Pflugers Arch. 1984 Apr;400(4):439-41. doi: 10.1007/BF00587546.

DOI:10.1007/BF00587546
PMID:6087269
Abstract

The effect of maitotoxin (MTX), the most potent marine toxin as yet known, was studied using the skeletal muscle of the larval meal worm, Tenebrio molitor. In normal saline, Tenebrio muscles responded with the spike to direct stimulation. In the saline containing tetraethylammonium (TEA) the all-or-none action potential which had characteristic plateau was elicited by membrane depolarization. When MTX (5 X 10(-9) to 10(-8) g/ml) in the TEA saline was added, the plateau of action potential was prolonged more than in the saline containing TEA alone. Furthermore, MTX lowered the threshold, so that action potentials were readily evoked in the saline containing MTX. In either case, effects, of MTX were antagonized by Co2+. These results suggest that MTX activates the voltage-dependent Ca2+ channels in the insect muscle.

摘要

利用黄粉虫幼虫(黄粉虫)的骨骼肌研究了已知最强效的海洋毒素——刺尾鱼毒素(MTX)的作用。在生理盐水中,黄粉虫肌肉对直接刺激产生锋电位反应。在含有四乙铵(TEA)的盐水中,膜去极化可引发具有特征性平台期的全或无动作电位。当在含TEA的盐水中加入MTX(5×10⁻⁹至10⁻⁸克/毫升)时,动作电位的平台期比仅含TEA的盐水延长得更多。此外,MTX降低了阈值,因此在含MTX的盐水中很容易诱发动作电位。在这两种情况下,MTX的作用都被Co²⁺拮抗。这些结果表明,MTX激活了昆虫肌肉中的电压依赖性Ca²⁺通道。

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引用本文的文献

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本文引用的文献

1
Ryanodine alteration of the contractile state of rat ventricular myocardium. Comparison with dog, cat, and rabbit ventricular tissues.大鼠心室肌收缩状态的兰尼碱改变。与犬、猫和兔心室组织的比较。
Circ Res. 1980 Mar;46(3):332-43. doi: 10.1161/01.res.46.3.332.
2
Contraction and increase in tissue calcium content induced by maitotoxin, the most potent known marine toxin, in intestinal smooth muscle.由已知最强效的海洋毒素 maitotoxin 诱导的肠道平滑肌收缩及组织钙含量增加。
Br J Pharmacol. 1983 May;79(1):3-5. doi: 10.1111/j.1476-5381.1983.tb10485.x.
3
Excitatory effect of the most potent marine toxin, maitotoxin, on the guinea-pig vas deferens.
刺尾鱼毒素对豚鼠和大鼠心肌中钙离子运动的作用机制。
Br J Pharmacol. 1985 Oct;86(2):385-91. doi: 10.1111/j.1476-5381.1985.tb08907.x.
4
Maitotoxin stimulates phosphoinositide breakdown in neuroblastoma hybrid NCB-20 cells.maitotoxin刺激神经母细胞瘤杂交细胞NCB - 20中的磷酸肌醇分解。
Cell Mol Neurobiol. 1987 Sep;7(3):317-22. doi: 10.1007/BF00711308.
5
Maitotoxin-activated single calcium channels in guinea-pig cardiac cells.海葵毒素激活豚鼠心脏细胞中的单个钙通道。
Br J Pharmacol. 1987 Nov;92(3):665-71. doi: 10.1111/j.1476-5381.1987.tb11370.x.
6
Ciguatoxin enhances quantal transmitter release from frog motor nerve terminals.雪卡毒素增强青蛙运动神经末梢的量子递质释放。
Br J Pharmacol. 1990 Apr;99(4):695-700. doi: 10.1111/j.1476-5381.1990.tb12991.x.
最具毒性的海洋毒素——刺尾鱼毒素对豚鼠输精管的兴奋作用。
J Pharmacol Exp Ther. 1983 Oct;227(1):199-204.
4
Ca2+ channel activating function of maitotoxin, the most potent marine toxin known, in clonal rat pheochromocytoma cells.已知最强效的海洋毒素——刺尾鱼毒素在克隆大鼠嗜铬细胞瘤细胞中的钙离子通道激活功能。
J Biol Chem. 1983 Sep 25;258(18):10944-9.
5
Contractile response of the rabbit aorta to maitotoxin, the most potent marine toxin.兔主动脉对最强大的海洋毒素—— maitotoxin的收缩反应。
J Physiol. 1983 Apr;337:711-21. doi: 10.1113/jphysiol.1983.sp014650.
6
Maitotoxin, a Ca2+ channel activator candidate.maitotoxin,一种钙通道激活剂候选物。
J Biol Chem. 1982 Jul 10;257(13):7287-89.
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Calcium channel.钙通道
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