Discriminative and affective stimulus effects of dihydropyridine calcium channel modulators: relationship to antialcohol effects.
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Summary
Comparison of the effects of DHPs in CTA and CPP paradigms suggests that the affective stimulus effects of these compounds are dissimilar, and that the mechanism underlying the latter effects is probably not related to the mechanism underlying the antialcohol effects of DHP VOCC modulators.
- Type
- review
- Published
- 1999-10-01
- Cited by
- 7
- References
- 31
- OpenAlex
- https://openalex.org/W69820850
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:6651070
Keywords
Nimodipine, Dihydropyridine, DHPS, Chemistry, Calcium channel
References
- Effects of calcium channel antagonists on the reinforcing properties of morphine, ethanol and cocaine as measured by place conditioning.
- Characterization of the pharmacokinetic interaction between nifedipine and ethanol in the rat.
- Comparison of the stimulus properties of ethanol and the Ca2+ channel antagonist nimodipine in rats.
- Effects of dihydropyridine Ca2+ channel blockers on the discriminative stimulus and the motor impairing effects of (+/-)-Bay K 8644.
- Effect of nimodipine, diltiazem and BAY K 8644 on the behavioural and neurochemical changes associated with naloxone-precipitated withdrawal in the rat. A comparison with clonidine.
- Effects of calcium channel inhibitors on ethanol effects and pharmacokinetics in healthy volunteers.
- BAY K 8644 enhances immobility in the mouse behavioral despair test, an effect blocked by nifedipine.
- Calcium channel agonist (−)-BAY k 8644 suppresses free and limited access intake of alcohol in genetic drinking rats
- Ca2+ agonists: new, sensitive probes for Ca2+ channels
- P.5.026 Effects of the calcium channel blocker, nimodipine, on the discriminative and reinforcing stimulus properties of alcohol
- Isradipine produces neither a conditioned place preference nor aversion.
- Discriminative stimulus properties of isradipine: effect of other calcium channel blockers.
- Effects of nimodipine and other calcium channel antagonists in alcohol-preferring AA rats.
- Blockade of ethanol discrimination by isradipine.
- RELATIONSHIP BETWEEN BASELINES OF EMOTIONAL BEHAVIOR AND SUBSEQUENT ETHANOL PREFERENCE IN ALCOHOL-PREFERRING AA RATS
- Central and peripheral effects of the dihydropyridine calcium channel activator BAY K 8644 in the rat.
- Unbiased cocaine conditioned place preferences (CPP) obscures conditioned locomotion, and nimodipine blockade of cocaine CPP is due to conditioned place aversions
- Isradipine is able to separate morphine-induced analgesia and place conditioning.
- Conditioned taste aversion and place preference induced by the calcium channel antagonist nimodipine in rats.
- Effects of calcium channel blockade on intravenous self-administration of ethanol in rats.
Cited by
- Maturation of rat cerebellar Purkinje cells reveals an atypical Ca2+ channel current that is inhibited by ω‐agatoxin IVA and the dihydropyridine (−)‐(S)‐Bay K8644
- REVIEW ON CPP: Measuring reward with the conditioned place preference (CPP) paradigm: update of the last decade
- Effects of Conditioned Food Aversions on Nutritional Behavior in Humans
- Selectivity of blocking of low- versus high-voltage activated calcium currents by the dihydropyridine derivatives Bay E5759 and Bay A4339 in neuroblastoma--glioma NG 108-15 cells.
- N-methyl-D-aspartate glutamate receptors and alcoholism: reward, dependence, treatment, and vulnerability.
- Attenuation of Ketamine Effects by Nimodipine Pretreatment in Recovering Ethanol Dependent Men: Psychopharmacologic Implications of the Interaction of NMDA and L-Type Calcium Channel Antagonists
- BAY-K 8644
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