Open AccessEffect of dibazol and its new derivatives on the mollusk ionic channels
Author(s) -
А. И. Вислобоков,
Leonid V. Myznikov,
Aleksandr Aleksandrovich Tarasenko,
Petr Dmitriyevich Shabanov
Publication year - 2013
Publication title -
obzory po kliničeskoj farmakologii i lekarstvennoj terapii
Language(s) - English
Resource type - Journals
eISSN - 2542-1875
pISSN - 1683-4100
DOI - 10.17816/rcf11326-32
Subject(s) - lymnaea stagnalis , chemistry , potassium , biophysics , membrane potential , intracellular , extracellular , calcium , ionic bonding , sodium , lymnaea , biochemistry , ion , biology , snail , ecology , organic chemistry
The changes in transmembrane calcium, sodium and potassium ionic currents after extracellular administration of dibazol (2-(phenylmethyl)-1H-benzimidazol hydrochloride) and its two new derivatives in concentrations of 1, 10, 100 and 1000 µM were studied by the method of intracellular dialysis and fixation of membrane potential in isolated neurons of the Lymnaea stagnalis mollusk. Dibazol in concentrations of 1 and 10 µM effected slightly on the ionic currents. High concentrations of dibazol (100 and 1000 µM) inhibited all currents in dose dependent manner with maximal effect on potassium currents amplitude. ЕС50 were 7.4 мМ for INa, 4.0 мМ for ICa, 83.9 µM for IKs,1 (one group of neurons) and 2.9 мМ for IKs,2 (the another group of neurons). The voltage-amper membrane characteristics shift was not registered, but the kinetics of currents development was changed. Dibazol was more effective in inhibition of ionic currents compared to its structural analogs.