A new glibenclamide-insensitive neuroselective hyperpolarizing agent.

Autor: Hunnicutt EJ Jr; Miles Institute for Dementia Research, West Haven, CT 06516., Davis JN, Chisholm JC
Jazyk: angličtina
Zdroj: European journal of pharmacology [Eur J Pharmacol] 1994 Aug 11; Vol. 261 (1-2), pp. R1-3.
DOI: 10.1016/0014-2999(94)90325-5
Abstrakt: We describe a novel compound, (-)-N-(2-ethoxyphenyl)-N'-(1,2,3-trimethylpropyl)-2-nitroethene-1, 1-diamine), Bay x9227, that demonstrates dose-dependent hyperpolarizing activity of remarkable potency (EC50 3 picomolar) and selectivity for CNS neurons and clonal neurotypic cells compared to smooth muscle cells. Single cell membrane potential measurements were obtained in physiologic buffer using the fluorescent probe, bisoxonol. Unlike K+ATP-channel activators including its (+)-enantiomer (Hoffman et al., 1993, Biochem. Biophys. Res. Commun. 190(2), 551), this activity was insensitive to glibenclamide antagonism. These data suggest a novel pharmacologic site for effecting neuroselective hyperpolarization.
Databáze: MEDLINE