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pubmed:abstractText |
The most potent marine toxin, maitotoxin (MTX) (10(-9) to 3 X 10(-8) g/ml) caused a slower contraction of the isolated guinea-pig vas deferens (second component) in a dose-dependent manner after the first rapid phasic contraction (first component). The second component of the MTX-induced contraction was markedly inhibited by phentolamine and reserpine, whereas the first component remained unaffected. Both components were inhibited or abolished by verapamil or a Ca-free medium, but were not affected by atropine, chlorpheniramine or tetrodotoxin. The tissue Ca content of the vas deferens was increased by MTX 10(-9) to 3 X 10(-8) g/ml) in a dose-dependent manner. Furthermore, MTX (10(-9) to 3 X 10(-8) g/ml) caused a dose-dependent release of norepinephrine from the tissue, which was inhibited or abolished by verapamil or a Ca-free medium. In Na+-free medium, MTX still caused a profound increase in the tissue Ca content and a marked release of norepinephrine from the vas deferens. These results suggest that the major part of the first component is the result of a direct action of MTX on smooth muscle membrane, whereas the second component is primarily the result of indirect action mediated through the norepinephrine release from the adrenergic nerve terminals. It is also suggested that both components are possibly due to an increased Ca++ permeability of the voltage sensitive Ca++ channels in smooth muscle and nerve membrane.
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