Dobrev D, Andreas K
Institute of Pharmacology and Toxicology, Faculty of Medicine, University of Technology, Dresden, Germany.
Neurochem Res. 1997 Sep;22(9):1085-93. doi: 10.1023/a:1027305016440.
We examined the involvement of voltage-activated Ca2+ channels (VACCs) on K+(50 mM)-evoked [3H]dopamine ([3H]DA) release from superfused rat striatal slices. Neither nifedipine nor nitrendipine modified K(+)-evoked [3H]DA release, indicating that L-type VACCs are not involved. K(+)-evoked [3H]DA release was partially inhibited by omega-CTx-GVIA and omega-Aga-IVA, and was abolished by 3 microM omega-CTx-MVIIC (IC50 approximately 128 nM), suggesting the involvement of N-, P-, or Q-type VACCs, respectively. Moreover, even subnanomolar concentrations of omega-CTx-MVIIC (0.1-0.5 nM) inhibited K(+)-evoked [3H]DA release by approximately 25%, suggesting the possible involvement of a still not classified (perhaps O-type?) Ca2+ channel subtype. The effects of omega-CTx-MVIIC (10-100 nM) and omega-CTx-GVIA (1 microM) were additive, suggesting that low nanomolar concentrations of omega-CTx-MVIIC does not interact with N-type VACCs. In conclusion, the K(+)-evoked [3H]DA release from rat striatal slices is mediated by entry of Ca2+ through omega-CTx-GVIA sensitive (N-type) as well as through omega-Aga-IVA (P-type) and omega-CTx-MVIIC (probably Q-type) sensitive VACCs.
我们研究了电压激活的Ca2+通道(VACCs)在50 mM K+诱发的[3H]多巴胺([3H]DA)从灌流大鼠纹状体切片释放过程中的作用。硝苯地平与尼群地平均未改变K+诱发的[3H]DA释放,表明L型VACCs未参与其中。K+诱发的[3H]DA释放被ω-芋螺毒素GVIA和ω-蜘蛛毒素-IVA部分抑制,并被3 μM ω-芋螺毒素MVIIC(IC50约为128 nM)完全消除,分别提示N型、P型或Q型VACCs参与其中。此外,即使是亚纳摩尔浓度的ω-芋螺毒素MVIIC(0.1 - 0.5 nM)也能抑制K+诱发的[3H]DA释放约25%,提示可能存在一种尚未分类(或许是O型?)的Ca2+通道亚型参与其中。ω-芋螺毒素MVIIC(10 - 100 nM)和ω-芋螺毒素GVIA(1 μM)的作用是相加的,表明低纳摩尔浓度的ω-芋螺毒素MVIIC不与N型VACCs相互作用。总之,K+诱发的大鼠纹状体切片[3H]DA释放是由Ca2+通过ω-芋螺毒素GVIA敏感(N型)以及ω-蜘蛛毒素-IVA(P型)和ω-芋螺毒素MVIIC(可能是Q型)敏感的VACCs内流介导的。