Role of opioidergic mechanisms and GABA uptake inhibition in the heroin-induced discriminative stimulus effects in rats.
Journal Title: Pharmacological Reports - Year 2005, Vol 57, Issue 6
Abstract
The present study was designed to investigate the involvement of opioidergic component as well as to study GABAergic mechanisms in the expression of heroin discrimination. Male Wistar rats were trained to discriminate heroin (0.5 mg/kg, ip) from saline (ip) in a two-choice water reinforced fixed ratio (FR) 20 drug discrimination paradigm. In substitution tests, heroin (0.0625-0.5 mg/kg) and morphine (0.5-2 mg/kg, ip) evoked a dose-dependent generalization for the drug lever-responding, while muscimol (1 mg/kg, ip, a GABA(A) receptor agonist) produced a weak partial substitution (ca. 48% heroin-lever responding). Neither tiagabine (2.5 mg/kg, ip; a GABA reuptake inhibitor), vigabatrin (75-150 mg/kg, ip; an irreversible inhibitor of GABA transaminase), nor baclofen (0.5 mg/kg, ip; a GABA(B) receptor agonist) substituted for heroin. In combination studies, the stimulus effects produced by heroin (0.5 mg/kg) or morphine (2 mg/kg) were dose-dependently blocked by opioid receptor antagonists naltrexone (0.1-1 mg/kg, ip), and naloxone (0.5-1 mg/kg, ip). The peripherally-acting naloxone methiodide at a dose of 1 mg/kg, ip did not alter, while at a dose of 10 mg/kg that penetrates across the blood-brain barrier, it reduced the stimulus effects of heroin or morphine. Pretreatment with tiagabine (2.5-5 mg/kg) produced a rightward shift of a heroin dose-response curve, while vigabatrin (75-300 mg/kg), baclofen (0.5-2.5 mg/kg) or muscimol (0.5-2 mg/kg) given prior to heroin (0.0625-0.5 mg/kg) failed to alter heroin discrimination. Our findings confirm previous studies on the significance of mu-opioidergic mechanisms in the expression of heroin discrimination and add the observation that selective inhibition of GABA reuptake, but not inhibition of GABA transaminase or direct stimulation of GABA(A) and GABA(B) receptors, can decrease the overall effects of heroin.
Authors and Affiliations
Wojciech Solecki, Tomasz Krówka, Małgorzata Filip, Ryszard Przewłocki
Study of the cytotoxicity and antioxidant capacity of N/OFQ(1-13)NH2 and its structural analogues.
The effect of side-chain shortening of N/OFQ(1-13)NH(2) at position 9 ([Orn(9)]N/OFQ(1-13)NH(2), [Dab(9)]N/OFQ(1-13)NH(2), [Dap(9)]N/OFQ(1-13)NH(2)) was studied regarding potential toxicity and antioxidant capacity. Stau...
Stiripentol. A novel antiepileptic drug.
Epilepsy is one of the most widespread pathologies of human brain, affecting approximately 1% of world population. Despite the development of new methods of seizure control, chronic administration of antiepileptic drugs...
Atherosclerotic risk among children taking antiepileptic drugs.
Epilepsy is a common chronic neurological disorder that requires long-term or sometimes lifetime therapy. Recent evidence indicates that prolonged use of antiepileptic drugs (AEDs) might modify some vascular risk factors...
Differential effects of glycine on the anticonvulsant activity of D-cycloserine and L-701,324 in mice.
The anticonvulsant effects of D-cycloserine, which is a partial agonist of the glycine/N-methyl-D-aspartate (NMDA) receptor, and L-701,324, which is a selective and potent antagonist that acts at the glycine site, were s...
Nitric oxide modulates the amphetamine effect on [(3)H]glucose uptake in the brain of rats prenatally exposed to lead.
Glucose is the main source of energy for the central nervous system (CNS). In this study, we examined the effects of the psychostimulant amphetamine (AMPH) and the neuronal mediator nitric oxide (NO) on [(3)H]glucose upt...