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sFTX - 3.3和FTX - 3.3对成熟大鼠小脑浦肯野细胞中Ca2+通道的差异抑制作用。

Differential inhibition of Ca2+ channels in mature rat cerebellar Purkinje cells by sFTX-3.3 and FTX-3.3.

作者信息

Dupere J R, Moya E, Blagbrough I S, Usowicz M M

机构信息

Department of Pharmacology, University of Bristol, U.K.

出版信息

Neuropharmacology. 1996 Jan;35(1):1-11. doi: 10.1016/0028-3908(95)00156-5.

Abstract

Synthetic funnel web spider toxin (sFTX-3.3) is a polyamine amide analogue of FTX, a toxin fraction isolated from the venom of the funnel web spider, Agelenopsis aperta, that blocks P-type Ca2+ channels. The structures of these polyamine containing compounds are not identical: sFTX-3.3 contains an amide carbonyl oxygen that is absent from the predicted structure of native FTX. Recently, a compound called FTX-3.3 was synthesized with the structure predicted for native FTX. We have compared the effects of polyamine amide sFTX-3.3 and polyamine FTX-3.3, on Ca2+ channel currents in the soma of mature rat cerebellar Purkinje neurons, in which the predominant Ca2+ channels are defined as P-type. Differential inhibition by sFTX-3.3 and FTX-3.3 revealed three populations of Ca2+ channels. One group, mediating approximately 66% of the current, was blocked by sFTX-3.3 with an IC50 (concentration producing half maximal inhibition) of 33 nM or by FTX-3.3 with an IC50 of 55 pM. A second population (5-25% of the total current) was inhibited by sFTX-3.3 with an IC50 of 33 nM, but was insensitive to FTX-3.3, while a third (10-30%) was blocked by FTX-3.3 with an IC50 of 125 nM and was resistant to sFTX-3.3. These channels also showed distinctive current-voltage relationships. Our results suggest that P-type Ca2+ channels in mature rat cerebellar Purkinje cells may be subdivided according to pharmacological and biophysical properties.

摘要

合成漏斗网蜘蛛毒素(sFTX - 3.3)是FTX的多胺酰胺类似物,FTX是从漏斗网蜘蛛(Agelenopsis aperta)毒液中分离出的一种毒素组分,可阻断P型Ca2 +通道。这些含多胺化合物的结构并不相同:sFTX - 3.3含有一个酰胺羰基氧,而天然FTX的预测结构中没有该基团。最近,一种名为FTX - 3.3的化合物被合成出来,其结构与天然FTX的预测结构一致。我们比较了多胺酰胺sFTX - 3.3和多胺FTX - 3.3对成熟大鼠小脑浦肯野神经元胞体中Ca2 +通道电流的影响,其中主要的Ca2 +通道被定义为P型。sFTX - 3.3和FTX - 3.3的差异抑制作用揭示了三类Ca2 +通道。第一组介导约66%的电流,被sFTX - 3.3以33 nM的IC50(产生半数最大抑制的浓度)阻断,或被FTX - 3.3以55 pM的IC50阻断。第二组(占总电流的5 - 25%)被sFTX - 3.3以33 nM的IC50抑制,但对FTX - 3.3不敏感,而第三组(10 - 30%)被FTX - 3.3以125 nM的IC50阻断,对sFTX - 3.3有抗性。这些通道还表现出独特的电流 - 电压关系。我们的结果表明,成熟大鼠小脑浦肯野细胞中的P型Ca2 +通道可能根据药理和生物物理特性进行细分。

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