Monoaminergic and local anesthetic components of cocaine's effects on kindled seizure expression

Male Long-Evans rats were kindled via daily electrical stimulation of the left prepyriform cortex. The animals were then used in two experiments which examined the pharmacological basis of cocaine's effects on three mutually exclusive components of the kindled seizure, which were the following:...

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Published inPharmacology, biochemistry and behavior Vol. 22; no. 3; pp. 427 - 434
Main Authors Russell, R.D., Stripling, J.S.
Format Journal Article
LanguageEnglish
Published New York, NY Elsevier Inc 01.03.1985
Elsevier Science
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Abstract Male Long-Evans rats were kindled via daily electrical stimulation of the left prepyriform cortex. The animals were then used in two experiments which examined the pharmacological basis of cocaine's effects on three mutually exclusive components of the kindled seizure, which were the following: (a) latency to clonus, (b) clonus duration, and (c) duration of AD outlasting clonus. The first experiment compared the effects produced by cocaine HCl (20 mg/kg, IP), lidocaine HCl (20 mg/kg, IP), and amphetamine sulfate (2.5 mg/kg, IP). The results indicated that both cocaine and lidocaine reduced the duration of kindled AD, latency to clonus, and duration of AD persisting beyond clonus, thus suggesting that these cocaine effects are mediated by local anesthetic meechanisms. Only cocaine reduced clonus duration, which suggest that this cocaine effect is not produced by a local anesthetic action. The second experiment examined the effects of cocaine following the adminiostration of three dose levels of the monoamine antagonists haloperidol, prazosin, yohimbine, propranolol, or metergoline (selected for their ability to block dopamine, alpha-1-norepinephrine, alpha-2-norepinephrine, beta-norepinephrine, and serotonin receptors, respectively). The results of this experiment found no support for a monoaminergic contribution to cocaine's effect on clonus latency or AD after clonus. However, results for prazosin, which reduced clonus duration and exhibited an additive effect with cocaine on this variable, suggest that cocaine's norepinephrine action (especially on the alpha-norepinephrine systems) may modulate clonus duration.
AbstractList Male Long-Evans rats were kindled via daily electrical stimulation of the left prepyriform cortex. The animals were then used in two experiments which examined the pharmacological basis of cocaine's effects on three mutually exclusive components of the kindled seizure, which were the following: (a) latency to clonus, (b) clonus duration, and (c) duration of AD outlasting clonus. The first experiment compared the effects produced by cocaine HCl (20 mg/kg, IP), lidocaine HCl (20 mg/kg, IP), and amphetamine sulfate (2.5 mg/kg, IP). The results indicated that both cocaine and lidocaine reduced the duration of kindled AD, latency to clonus, and duration of AD persisting beyond clonus, thus suggesting that these cocaine effects are mediated by local anesthetic meechanisms. Only cocaine reduced clonus duration, which suggest that this cocaine effect is not produced by a local anesthetic action. The second experiment examined the effects of cocaine following the adminiostration of three dose levels of the monoamine antagonists haloperidol, prazosin, yohimbine, propranolol, or metergoline (selected for their ability to block dopamine, alpha-1-norepinephrine, alpha-2-norepinephrine, beta-norepinephrine, and serotonin receptors, respectively). The results of this experiment found no support for a monoaminergic contribution to cocaine's effect on clonus latency or AD after clonus. However, results for prazosin, which reduced clonus duration and exhibited an additive effect with cocaine on this variable, suggest that cocaine's norepinephrine action (especially on the alpha-norepinephrine systems) may modulate clonus duration.
Male Long-Evans rats were kindled via daily electrical stimulation of the left prepyriform cortex. The animals were then used in two experiments which examined the pharmacological basis of cocaine's effects on three mutually exclusive components of the kindled seizure, which were the following: (a) latency to clonus, (b) clonus duration, and (c) duration of AD outlasting clonus. The first experiment compared the effects produced by cocaine HCl (20 mg/kg, IP), lidocaine HCl (20 mg/kg, IP), and amphetamine sulfate (2.5 mg/kg, IP). The results indicated that both cocaine and lidocaine reduced the duration of kindled AD, latency to clonus, and duration of AD persisting beyond clonus, thus suggesting that these cocaine effects are mediated by local anesthetic mechanisms. Only cocaine reduced clonus duration, which suggests that this cocaine effect is not produced by a local anesthetic action. The second experiment examined the effects of cocaine following the administration of three dose levels of the monoamine antagonists haloperidol, prazosin, yohimbine, propranolol, or metergoline (selected for their ability to block dopamine, alpha-1-norepinephrine, alpha-2-norepinephrine, beta-norepinephrine, and serotonin receptors, respectively). The results of this experiment found no support for a monoaminergic contribution to cocaine's effect on clonus latency or AD after clonus. However, results for prazosin, which reduced clonus duration and exhibited an additive effect with cocaine on this variable, suggest that cocaine's norepinephrine action (especially on the alpha-norepinephrine systems) may modulate clonus duration.
Male Long-Evans rats were kindled via daily electrical stimulatin of the left prepyriform cortex. The animals were then used in two experiments which examined the pharmacological basis of cocaine's effects on three mutually exclusive components of the kindled seizure, which were the following: latency to clonus, clonus duration, and duration of AD outlasting clonus. Results indicated that both cocaine and lidocaine reduced the duration of kindled AD, latency to clonus, and duration of AD persisting beyond clonus, thus suggesting that these cocaine effects are mediated by local anesthetic mechanisms. Only cocaine reduced clonus duration, which suggests that this cocaine effect is not produced by a local anesthetic action.
Author Stripling, J.S.
Russell, R.D.
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Issue 3
Keywords Prepyriform cortex
Prazosin
Metergoline
Amphetamine
Rat
Yohimbine
Kindling
Cocaine
Haloperidol
Lidocaine
Propranolol
Local anesthetic
Animal
Language English
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Snippet Male Long-Evans rats were kindled via daily electrical stimulation of the left prepyriform cortex. The animals were then used in two experiments which examined...
Male Long-Evans rats were kindled via daily electrical stimulatin of the left prepyriform cortex. The animals were then used in two experiments which examined...
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SubjectTerms Amphetamine
Amphetamine - pharmacology
Anesthetics, Local
Animals
Biogenic Amines - metabolism
Biological and medical sciences
Cocaine
Cocaine - pharmacology
Drug Interactions
Haloperidol
Haloperidol - pharmacology
Kindling
Kindling, Neurologic - drug effects
Lidocaine
Lidocaine - pharmacology
Male
Medical sciences
Metergoline
Metergoline - pharmacology
Miscellaneous
Neuropharmacology
Pharmacology. Drug treatments
Prazosin
Prazosin - pharmacology
Prepyriform cortex
Propranolol
Propranolol - pharmacology
Rat
Rats
Seizures - chemically induced
Yohimbine
Yohimbine - pharmacology
Title Monoaminergic and local anesthetic components of cocaine's effects on kindled seizure expression
URI https://dx.doi.org/10.1016/0091-3057(85)90044-9
https://www.ncbi.nlm.nih.gov/pubmed/3991758
https://search.proquest.com/docview/14345455
Volume 22
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