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Neuroscience ; 121(2): 387-98, 2003.
Article in English | MEDLINE | ID: mdl-14521997

ABSTRACT

The purpose of this study was to investigate the role that mu and delta opioid receptor blockade has upon stimulant-induced behavior and neuropeptide gene expression in the striatum. Acute administration of amphetamine (2.5 mg/kg i.p.) caused an increase in behavioral activity and preprodynorphin, substance P, and preproenkephalin mRNA expression. Intrastriatal infusion of the mu opioid antagonist, H-D-Phe-Cys-Tyr-D-Trp-Arg-Thr-Pen-Thr-NH(2) (CTAP), or the delta opioid antagonist, H-Tyr-Tic[CH(2)NH]-Phe-Phe-OH (TIPPpsi), significantly decreased amphetamine-induced vertical activity. However, only CTAP reduced amphetamine-induced distance traveled. Quantitative in situ hybridization histochemistry revealed that CTAP blocked amphetamine-induced preprodynorphin and substance P mRNA. However, preproenkephalin mRNA levels in the dorsal striatum were increased to the same extent by CTAP, amphetamine, or a combination of the two drugs. In contrast, TIPPpsi significantly decreased amphetamine-induced mRNA expression of all three neuropeptides. These data indicate that both mu and delta receptor subtypes differentially regulate amphetamine-induced behavior and neuropeptide gene expression in the rat striatum.


Subject(s)
Amphetamine/pharmacology , Central Nervous System Stimulants/pharmacology , Corpus Striatum/drug effects , Neuropeptides/metabolism , Receptors, Opioid, delta/metabolism , Receptors, Opioid, mu/metabolism , Animals , Behavior, Animal/drug effects , Corpus Striatum/metabolism , Corpus Striatum/physiology , Drug Interactions , In Situ Hybridization , Male , Motor Activity/drug effects , Narcotic Antagonists/pharmacology , Neuropeptides/genetics , Oligopeptides/pharmacology , Peptide Fragments , Peptides/pharmacology , RNA, Messenger/metabolism , Radiographic Image Enhancement , Random Allocation , Rats , Rats, Sprague-Dawley , Receptors, Opioid, delta/antagonists & inhibitors , Receptors, Opioid, delta/physiology , Receptors, Opioid, mu/antagonists & inhibitors , Receptors, Opioid, mu/physiology , Somatostatin
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