Scheer H W
Department of Pharmacology, Université de Montréal, Quebec, Canada.
J Neurochem. 1989 May;52(5):1590-7. doi: 10.1111/j.1471-4159.1989.tb09213.x.
The interactions between alpha-latrotoxin (alpha-LTx), a neurosecretagogue purified from the venom of the black widow spider, and the trivalent cations Al3+, Y3+, La3+, Gd3+, and Yb3+ were investigated in rat striatal synaptosomal preparations. All trivalent cations tested were inhibitors of alpha-LTx-induced [3H]dopamine [( 3H]DA) release (order of potency: Yb3+ greater than Gd3+ approximately Y3+ greater than La3+ greater than Al3+). Only with Al3+ could inhibition of [3H]DA release be attributed to a block of 125I-alpha-LTx specific binding to synaptosomal preparations. The inhibitory effect of trivalent ions was reversible provided synaptosomes were washed with buffer containing EDTA. Trivalent ions also inhibited alpha-LTx-induced [3H]DA release at times when alpha-LTx-stimulated release was already evident. alpha-LTx-induced synaptosomal membrane depolarization was blocked by La3+, but not affected by Gd3+, Y3+, and Yb3+. alpha-LTx-stimulated uptake of 45Ca2+ was inhibited by all trivalent cations tested. These results demonstrate that there exist at least three means by which trivalent cations can inhibit alpha-LTx action in rat striatal synaptosomal preparations: (1) inhibition of alpha-LTx binding (Al3+); (2) inhibition of alpha-LTx-induced depolarization (La3+); and (3) inhibition of alpha-LTx-induced 45Ca2+ uptake (Gd3+, Y3+, Yb3+, La3+).
在大鼠纹状体突触体标本中研究了从黑寡妇蜘蛛毒液中纯化的神经分泌素α-拉托毒素(α-LTx)与三价阳离子Al3+、Y3+、La3+、Gd3+和Yb3+之间的相互作用。所有测试的三价阳离子都是α-LTx诱导的[3H]多巴胺[(3H]DA)释放的抑制剂(效力顺序:Yb3+>Gd3+≈Y3+>La3+>Al3+)。只有Al3+对[3H]DA释放的抑制可归因于阻断125I-α-LTx与突触体标本的特异性结合。如果用含有EDTA的缓冲液洗涤突触体,三价离子的抑制作用是可逆的。在α-LTx刺激的释放已经明显时,三价离子也抑制α-LTx诱导的[3H]DA释放。α-LTx诱导的突触体膜去极化被La3+阻断,但不受Gd3+、Y3+和Yb3+影响。所有测试的三价阳离子都抑制α-LTx刺激的45Ca2+摄取。这些结果表明,在大鼠纹状体突触体标本中,三价阳离子至少有三种方式可以抑制α-LTx的作用:(1)抑制α-LTx结合(Al3+);(2)抑制α-LTx诱导的去极化(La3+);(3)抑制α-LTx诱导的45Ca2+摄取(Gd3+、Y3+、Yb3+、La3+)。