Philanthotoxin inhibits Ca2+ currents in rat hippocampal CA1 neurons.
H Karst, M Joëls, W J Wadman, T Piek
Index: Eur. J. Pharmacol. 270 , 357-360, (1994)
Full Text: HTML
Abstract
The wasp venom philanthotoxin-4.3.3 (PhTX-4.3.3) is an antagonist of glutamate transmission in the insect as well as in the mammalian brain. It was recently shown that PhTX-4.3.3 inhibits the N-methyl-D-aspartate (NMDA) transmission in rat hippocampus. In this study we show that dideaza-philanthotoxin-12 (dideaza-PhTX-12), an analogue of PhTX-4.3.3, is a potent antagonist of voltage-dependent Ca2+ currents in rat hippocampal CA1 neurons. At a concentration of 10 microM it reduces the Ca2+ current to 40%. Two voltage-dependent potassium currents, the A current and the delayed rectifier, were hardly affected by dideaza-PhTX-12, indicating selectivity of the drug for Ca2+ currents. As a consequence the philanthotoxins will inhibit the calcium influx via voltage dependent as well as NMDA mediaded calcium channels and thus reduce excitability in the hippocampus.
Related Compounds
Related Articles:
Effects of philanthotoxin-343 on CA1 pyramidal neurons of rat hippocampus in vitro.
1992-12-01
[Eur. J. Pharmacol. 228 , 201-206, (1992)]
1992-06-01
[Comp. Biochem. Physiol. 102C , 267-272, (1992)]
Selective antagonism of native and cloned kainate and NMDA receptors by polyamine-containing toxins.
1993-09-01
[J. Pharmacol. Exp. Ther. 266 , 1573-1580, (1993)]