Block by ruthenium red of cloned neuronal voltage-gated calcium channels

Citation
Sm. Cibulsky et Wa. Sather, Block by ruthenium red of cloned neuronal voltage-gated calcium channels, J PHARM EXP, 289(3), 1999, pp. 1447-1453
Citations number
34
Categorie Soggetti
Pharmacology & Toxicology
Journal title
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS
ISSN journal
00223565 → ACNP
Volume
289
Issue
3
Year of publication
1999
Pages
1447 - 1453
Database
ISI
SICI code
0022-3565(199906)289:3<1447:BBRROC>2.0.ZU;2-G
Abstract
The dye ruthenium red (RuR) has diverse experimental uses, including block of ion channels. RuR is a well described antagonist of one class of intrace llular Ca2+ release channels, the ryanodine receptors, but recently this co mpound has also been identified as a putative blocker of voltage-gated calc ium channels of the surface membrane involved in neurotransmitter release. Using electrophysiological methods, we have studied the action of RuR upon pure populations of neuronal voltage-gated ion channels heterologously expr essed in Xenopus laevis oocytes. All four channel types studied, including class A (P/Q-type), class B (N-type), class C (L-type), and class E channel s, are sensitive to RuR, with IC50 values ranging from 0.7 to 67.1 mu M. Bl ock Of class C and class E channels most likely results from 1:1 binding of ruthenium red at a site in the extracellular entrance to the pore, resulti ng in obstruction of permeant ion flux through these channels. The mechanis m of block of class A and class B channels is more complex, requiring bindi ng of more than one molecule of RuR per channel.