Omeprazole has long been used as an effective agent to treat peptic ulcer.
Recent studies have shown that in addition to inhibiting the H+-K(+)ATPase.
it also inhibits carbonic anhydrase (CA) types I, II and IV. This led us t
o investigate its anticonvulsant effect in a rat model of electroconvulsion
. Since other carbonic anhydrase inhibitors like acetazolamide induce toler
ance upon repeated use. we tested the tolerance potential of omeprazole upo
n repeated administration of up to 1 week. The animals were divided into fo
ur groups receiving normal saline, omeprazole 0.5, 1 or 2 mg/kg intraperito
neally. CC50, i.e. the threshold current inducing tonic hind limb extension
in 50% of the rats was established using a technoconvulsometer which deliv
ers currents of varying intensity via ear clip electrodes. The CC50 was est
ablished 30 min after injection of omeprazole. In another group of rats, om
eprazole 2 mg/kg was given for 6 days and the CC50 determined on days 0, 1,
3 and 6. Also the concentration of omeprazole in the brain was determined
using high performance liquid chromatography. The CC50, in vehicle-treated
rats was 98 mA, which increased to 126, 135 and 162 mA with 0.5, 1 and 2 mg
/kg of omeprazole, respectively. On repeat-dose studies the CC50 on day 0 w
as 96 mA, on day 1 166 mA, on day 3 129 mA and on day 6 102 mA. The average
brain concentration of omeprazole was 53.2 +/- 6.9 ng/g of brain tissue. I
n conclusion, this study has shown omeprazole to be an effective anticonvul
sant, but rapidly develops tolerance to its anticonvulsant action. This stu
dy can stimulate interest in the development of agents with dual function -
inhibition of CA as well as the accompanying Na+-K+ ATPase - and such agen
ts may prove to be effective anticonvulsants without exhibiting tolerance.
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