Chronic dihydropyridine treatment can reverse the behavioural consequences of and prevent adaptations to, chronic ethanol treatment
- PMID: 1834295
- PMCID: PMC1907826
- DOI: 10.1111/j.1476-5381.1991.tb09845.x
Chronic dihydropyridine treatment can reverse the behavioural consequences of and prevent adaptations to, chronic ethanol treatment
Abstract
1. Chronic treatment with the dihydropyridine calcium channel antagonist, nitrendipine, given concurrently with ethanol, prevented the ethanol withdrawal syndrome in mice, even though the chronic nitrendipine treatment was stopped 24 h or 48 h before the withdrawal testing. 2. This effect was seen in two strains of mice with different methods of ethanol administration. Nitrendipine was effective when given for two weeks but not after only two days' treatment. 3. Two other dihydropyridine calcium antagonists, nimodipine and PN 200-110, given chronically with ethanol, also prevented the withdrawal syndrome. The tests were again made 24 h after the last administration of dihydropyridine. 4. The chronic nitrendipine treatment also prevented the rise in the number of central dihydropyridine binding sites that occurs on chronic ethanol administration. 5. Chronic administration of nitrendipine alone did not cause any withdrawal behaviour. 6. Chronic nitrendipine treatment did not affect the seizure threshold to bicuculline in mice that were not given ethanol. 7. Whole brain concentration measurements showed that the effects were not due to residual nitrendipine in the CNS at the time of withdrawal testing or to differences in central ethanol concentrations during the treatment. 8. It is suggested that the results provide evidence for a functional role for dihydropyridine-sensitive calcium channels in ethanol dependence.
Similar articles
-
The differential effects of felodipine and nitrendipine on cerebral dihydropyridine binding ex vivo and the ethanol withdrawal syndrome in mice.Br J Pharmacol. 1994 Aug;112(4):1017-24. doi: 10.1111/j.1476-5381.1994.tb13184.x. Br J Pharmacol. 1994. PMID: 7524989 Free PMC article.
-
Dihydropyridine-sensitive calcium channels and barbiturate tolerance and withdrawal.Pharmacol Biochem Behav. 1994 Mar;47(3):675-80. doi: 10.1016/0091-3057(94)90173-2. Pharmacol Biochem Behav. 1994. PMID: 8208788
-
Selectivity of the protective effects of dihydropyridine calcium channel antagonists against the ethanol withdrawal syndrome.Brain Res. 2002 Mar 15;930(1-2):111-22. doi: 10.1016/s0006-8993(02)02236-9. Brain Res. 2002. PMID: 11879801
-
Calcium channel antagonists prevent adaptive responses to ethanol.Alcohol Alcohol Suppl. 1993;2:263-7. Alcohol Alcohol Suppl. 1993. PMID: 7748308 Review.
-
Neuropsychological profiles of calcium antagonists.Fundam Clin Pharmacol. 1989;3 Suppl:71s-78s. doi: 10.1111/j.1472-8206.1989.tb00477.x. Fundam Clin Pharmacol. 1989. PMID: 2693293 Review.
Cited by
-
Nitrendipine prevents the decrease caused by chronic ethanol intake in the maintenance of tetanic long-term potentiation.Exp Brain Res. 1995;103(1):1-8. doi: 10.1007/BF00241959. Exp Brain Res. 1995. PMID: 7615026
-
Interactions between diltiazem and ethanol: differences from those seen with dihydropyridine calcium channel antagonists.Psychopharmacology (Berl). 1994 Mar;114(2):329-36. doi: 10.1007/BF02244856. Psychopharmacology (Berl). 1994. PMID: 7838926
-
Psychopharmacological properties of calcium channel inhibitors.Psychopharmacology (Berl). 1992;109(1-2):12-29. doi: 10.1007/BF02245476. Psychopharmacology (Berl). 1992. PMID: 1365644 Review.
-
Concurrent nimodipine attenuates the withdrawal signs and the increase of cerebral dihydropyridine binding after chronic morphine treatment in rats.Naunyn Schmiedebergs Arch Pharmacol. 1993 May;347(5):483-6. doi: 10.1007/BF00166739. Naunyn Schmiedebergs Arch Pharmacol. 1993. PMID: 8321324
-
Hypoglycaemic brain damage: effect of a dihydropyridine calcium channel antagonist in rats.Diabetologia. 1996 Feb;39(2):129-34. doi: 10.1007/BF00403954. Diabetologia. 1996. PMID: 8635663
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources