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Characterization of dihydropyridine-sensitive calcium channels in rat brain synaptosomes.

We examined the effects of dihydropyridine Ca2+-channel agonists on synaptosomal voltage-dependent Ca2+ entry and endogenous dopamine release. The (-) isomer of Bay K 8644 and the (+) isomer of Sandoz compound 202-791 were 100-1000 times more potent than their respective opposite enantiomers in enha...

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發表在:Proc Natl Acad Sci U S A
Principais autores: Woodward, J J, Cook, M E, Leslie, S W
格式: Artigo
語言:Inglês
出版: National Academy of Sciences 1988
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在線閱讀:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC282192/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2459704/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.85.19.7389
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