The rare earth lanthanide gadolinium (Gd3+), in concentrations ranging from 1 to 100 muM, reduced the elevation of intracellular Ca2+ concentration [Ca2+]i, monitored by means of the fluorescent probe fura-2. It also decreased the influx of Ca-45(2+) through voltage sensitive calcium channels (VSCC), induced by 55 mM K+ in Percoll-purified brain synaptosomes. By contrast, Gd3+ (0.1-30 muM) did not interfere with Na+-dependent Ca-45(2+) uptake, a process which expresses Na+-Ca2+ exchange activity. The aminoglycoside neomycin displayed a similar pattern of activity although at higher concentrations (300-1000 muM). At the same range of concentrations (100 and 300 muM), the phenylalkylamine, verapamil, blocked both Ca2+ entry through VSCC and Ca2+ influx through the Na+-Ca2+ exchanger. Finally, nimodipine failed to prevent Ca-45(2+) influx in either case, and fura-2 monitored [Ca2+]i elevation induced by high K+- or Na+-dependent Ca-45(2+) uptake. Collectively, the data obtained in the present study indicate that Gd3+ and neomycin can be considered to be valid pharmacological tools for selective blocking of VSCC in cerebral nerve terminals, without any concomitant interference with the Na+-Ca2+ antiporter, whereas the inhibitory action of verapamil does not discriminate between Ca2+ entry through VSCC or the antiporter.
GADOLINIUM AND NEOMYCIN BLOCK VOLTAGE-SENSITIVE CA2+ CHANNELS WITHOUT INTERFERING WITH THE NA+-CA2+ ANTIPORTER IN BRAIN NERVE-ENDINGS
TAGLIALATELA, Maurizio;
1993-01-01
Abstract
The rare earth lanthanide gadolinium (Gd3+), in concentrations ranging from 1 to 100 muM, reduced the elevation of intracellular Ca2+ concentration [Ca2+]i, monitored by means of the fluorescent probe fura-2. It also decreased the influx of Ca-45(2+) through voltage sensitive calcium channels (VSCC), induced by 55 mM K+ in Percoll-purified brain synaptosomes. By contrast, Gd3+ (0.1-30 muM) did not interfere with Na+-dependent Ca-45(2+) uptake, a process which expresses Na+-Ca2+ exchange activity. The aminoglycoside neomycin displayed a similar pattern of activity although at higher concentrations (300-1000 muM). At the same range of concentrations (100 and 300 muM), the phenylalkylamine, verapamil, blocked both Ca2+ entry through VSCC and Ca2+ influx through the Na+-Ca2+ exchanger. Finally, nimodipine failed to prevent Ca-45(2+) influx in either case, and fura-2 monitored [Ca2+]i elevation induced by high K+- or Na+-dependent Ca-45(2+) uptake. Collectively, the data obtained in the present study indicate that Gd3+ and neomycin can be considered to be valid pharmacological tools for selective blocking of VSCC in cerebral nerve terminals, without any concomitant interference with the Na+-Ca2+ antiporter, whereas the inhibitory action of verapamil does not discriminate between Ca2+ entry through VSCC or the antiporter.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
