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贻贝 Mytilus galloprovincialis Lamarck, 1819 的幼虫变态对神经递质阻滞剂和四乙铵的反应

Larval metamorphosis of the mussel Mytilus galloprovincialis Lamarck, 1819 in response to neurotransmitter blockers and tetraethylammonium.

机构信息

College of Fisheries and Life Science, Shanghai Ocean University, Shanghai, China.

出版信息

Biofouling. 2011 Feb;27(2):193-9. doi: 10.1080/08927014.2011.553717.

Abstract

The metamorphic response of pediveliger larvae of Mytilus galloprovincialis to the neurotransmitter blockers chlorpromazine, amitriptyline, rauwolscine, idazoxan, atenolol and butoxamine, and to tetraethylammonium chloride (TEA) was investigated through a series of bioassays. Chlorpromazine, amitriptyline and idazoxin inhibited larval metamorphosis induced by 10⁻⁴ M epinephrine. The concentration that inhibited metamorphosis by 50% (IC₅₀) for chlorpromazine and amitriptyline was 1.6 x 10⁻⁶ M and 6.6 x 10⁻⁵ M, respectively. Idazoxan was less effective with an IC₅₀ of 4.4 x 10¹³ M. Moreover, these three inhibitors showed no toxicity at any of the concentrations tested. The larval metamorphic response to K+ was not inhibited by 10⁻³ M tetraethylammonium chloride after 96 h. Thus, the neurotransmitter blockers chlorpromazine and amitriptyline are inhibitors of larval metamorphosis, and will be useful tools for antifouling studies.

摘要

通过一系列生物测定法研究了贻贝幼虫豆形游走幼虫对神经递质阻滞剂氯丙嗪、阿米替林、劳沃尔西恩、伊达唑、阿替洛尔和丁氧胺以及氯化四乙铵(TEA)的变形反应。氯丙嗪、阿米替林和伊达唑抑制了 10⁻⁴ M 肾上腺素诱导的幼虫变态。氯丙嗪和阿米替林抑制变态的 50%浓度(IC₅₀)分别为 1.6 x 10⁻⁶ M 和 6.6 x 10⁻⁵ M。伊达唑的效果较差,IC₅₀为 4.4 x 10¹³ M。此外,在测试的任何浓度下,这三种抑制剂均没有毒性。96 小时后,10⁻³ M 四乙基氯化铵对 K+的幼虫变态反应没有抑制作用。因此,神经递质阻滞剂氯丙嗪和阿米替林是幼虫变态的抑制剂,将成为防污研究的有用工具。

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