Mas R, Menéndez R, Garateix A, Garcia M, Chávez M
Neuroscience Branch, National Scientific Research Center, Havana, Cuba.
Neuroscience. 1989;33(2):269-73. doi: 10.1016/0306-4522(89)90206-6.
The effects of a high molecular weight toxin from Physalia physalis (P3) were investigated on glutamate evoked potentials in snail (Zachrysia guanesis) neurons and in crayfish (Cambarus clarkii) neuromuscular junction. The glutamate evoked potentials of snail neurons were reversibly blocked by P3 in a dose-dependent manner (2-200 microM). A reversible blocking action was also found for P3 on excitatory junctional potentials and on glutamate potentials of crayfish at a concentration range of 6 nM-60 microM. Experiments carried out with independent stimulation of the excitatory and inhibitory nerves showed that the effect of P3 (60 nM-10 microM) was exerted predominantly on excitatory junctional potentials. However, at higher doses (greater than 10 microM) a slight reduction of the inhibitory potentials was also observed. These results suggest that P3 reversibly blocks glutamate receptors. Thus, it could be a promising tool for further studies on glutamatergic transmission.
研究了来自僧帽水母的一种高分子量毒素(P3)对蜗牛(Zachrysia guanesis)神经元和小龙虾(克氏原螯虾)神经肌肉接头处谷氨酸诱发电位的影响。蜗牛神经元的谷氨酸诱发电位被P3以剂量依赖性方式(2 - 200微摩尔)可逆性阻断。在6纳摩尔至60微摩尔的浓度范围内,还发现P3对小龙虾的兴奋性接头电位和谷氨酸电位有可逆性阻断作用。对兴奋性神经和抑制性神经进行独立刺激的实验表明,P3(60纳摩尔至10微摩尔)的作用主要施加于兴奋性接头电位。然而,在较高剂量(大于10微摩尔)时,也观察到抑制性电位略有降低。这些结果表明,P3可逆性阻断谷氨酸受体。因此,它可能是进一步研究谷氨酸能传递的一个有前景的工具。