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Influence of calcium channel inhibitors upon the anticonvulsant efficacy of common antiepileptics against pentylenetetrazol-induced convulsions in mice.
- Source :
-
Neuropharmacology [Neuropharmacology] 1990 Oct; Vol. 29 (10), pp. 943-8. - Publication Year :
- 1990
-
Abstract
- Among three calcium channel inhibitors studied, nifedipine (20 mg/kg) moderately inhibited pentylenetetrazol (115 mg/kg, s.c.)-induced convulsions, whilst diltiazem (up to 20 mg/kg) and verapamil (up to 20 mg/kg) were without effect. The combinations of nifedipine (10 and 20 mg/kg) with valproate (100 mg/kg) or phenobarbital (6.25 mg/kg) resulted in significant protection against pentylenetetrazol-induced seizures. Combined treatment of nifedipine (5-20 mg/kg) with ethosuximide (100 mg/kg) also provided a clearcut anticonvulsant action. The antiepileptic drugs alone, in the above doses, were ineffective. The combination of diltiazem (10-20 mg/kg) and ethosuximide (100 mg/kg) produced protection against pentylenetetrazol, comparable to that of ethosuximide (200 mg/kg) alone. No pharmacokinetic interactions were found in the case of ethosuximide, whilst nifedipine (10 mg/kg) increased the levels of phenobarbital and valproate in plasma. The combination of diltiazem with the remaining antiepileptics were ineffective. Verapamil (up to 20 mg/kg) was without effect upon the action of the antiepileptic drugs tested. Finally, none of the calcium channel inhibitors studied influenced the action of diazepam (0.2 mg/kg). It may be concluded that combinations of ethosuximide, with either nifedipine or diltiazem, may be promising for the treatment of absence epilepsy.
- Subjects :
- Animals
Diltiazem pharmacology
Drug Therapy, Combination
Ethosuximide therapeutic use
Male
Mice
Nifedipine therapeutic use
Pentylenetetrazole
Phenobarbital therapeutic use
Reference Values
Seizures chemically induced
Seizures physiopathology
Valproic Acid therapeutic use
Verapamil therapeutic use
Anticonvulsants therapeutic use
Calcium Channel Blockers therapeutic use
Seizures drug therapy
Subjects
Details
- Language :
- English
- ISSN :
- 0028-3908
- Volume :
- 29
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- Neuropharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 2255386
- Full Text :
- https://doi.org/10.1016/0028-3908(90)90145-h