GABA mechanisms in the pedunculopontine tegmental nucleus influence particular aspects of nicotine self-administration selectively in the rat

The pedunculopontine tegmental nucleus (PPTg) is part of the neuronal circuit activated by self-administered nicotine. The cholinergic neurons of the PPTg comprise a prominent projection to midbrain dopamine neurons. However, anatomical studies of Fos expression suggest that nicotine targets primari...

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Veröffentlicht in:Psychopharmacologia 2001-11, Vol.158 (2), p.190-197
Hauptverfasser: CORRIGALL, William A, COEN, Kathleen M, JIANHUA ZHANG, ADAMSON, K. Laurel
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creator CORRIGALL, William A
COEN, Kathleen M
JIANHUA ZHANG
ADAMSON, K. Laurel
description The pedunculopontine tegmental nucleus (PPTg) is part of the neuronal circuit activated by self-administered nicotine. The cholinergic neurons of the PPTg comprise a prominent projection to midbrain dopamine neurons. However, anatomical studies of Fos expression suggest that nicotine targets primarily non-cholinergic neurons in the PPTg, especially GABAergic and glutamatergic neurons. The objective of these experiments was to examine the role of GABA manipulations in the PPTg on nicotine self-administration. Rats trained to self-administer nicotine or cocaine intravenously were prepared with brain microcannulae directed to the PPTg. Intra-PPTg microinfusions of the GABA agonists muscimol (10-50 ng) and baclofen (30-60 ng) reduced nicotine self-administration maintained on a fixed-ratio schedule of reinforcement (30 microg/kg per infusion); self-administration of cocaine (0.3 mg/kg per infusion) under an identical schedule was not affected. Muscimol and baclofen were also examined after intra-PPTg microinfusion in animals trained to self-administer nicotine on a progressive-ratio schedule (10 and 30 microg/kg per infusion). Progressive-ratio responding was sensitive to pharmacological manipulations such as a change in the nicotine dose available for self-administration, or intra-PPTg microinfusion of the nicotinic antagonist dihydro-beta-erythroidine (30 microg). However, nicotine self-administration on a progressive-ratio schedule was not altered by intra-PPTg microinfusions of GABA agonists. These data confirm that the PPTg is involved in nicotine self-administration, a conclusion that is independent of the schedule of reinforcement that is used. GABAergic mechanisms in the PPTg play a selective role in nicotine reinforcement compared to cocaine, and that role is restricted to the characteristics of reinforcement measured by fixed-ratio responding.
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Laurel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>GABA mechanisms in the pedunculopontine tegmental nucleus influence particular aspects of nicotine self-administration selectively in the rat</atitle><jtitle>Psychopharmacologia</jtitle><addtitle>Psychopharmacology (Berl)</addtitle><date>2001-11-01</date><risdate>2001</risdate><volume>158</volume><issue>2</issue><spage>190</spage><epage>197</epage><pages>190-197</pages><issn>0033-3158</issn><eissn>1432-2072</eissn><coden>PSYPAG</coden><abstract>The pedunculopontine tegmental nucleus (PPTg) is part of the neuronal circuit activated by self-administered nicotine. The cholinergic neurons of the PPTg comprise a prominent projection to midbrain dopamine neurons. However, anatomical studies of Fos expression suggest that nicotine targets primarily non-cholinergic neurons in the PPTg, especially GABAergic and glutamatergic neurons. The objective of these experiments was to examine the role of GABA manipulations in the PPTg on nicotine self-administration. Rats trained to self-administer nicotine or cocaine intravenously were prepared with brain microcannulae directed to the PPTg. Intra-PPTg microinfusions of the GABA agonists muscimol (10-50 ng) and baclofen (30-60 ng) reduced nicotine self-administration maintained on a fixed-ratio schedule of reinforcement (30 microg/kg per infusion); self-administration of cocaine (0.3 mg/kg per infusion) under an identical schedule was not affected. Muscimol and baclofen were also examined after intra-PPTg microinfusion in animals trained to self-administer nicotine on a progressive-ratio schedule (10 and 30 microg/kg per infusion). Progressive-ratio responding was sensitive to pharmacological manipulations such as a change in the nicotine dose available for self-administration, or intra-PPTg microinfusion of the nicotinic antagonist dihydro-beta-erythroidine (30 microg). However, nicotine self-administration on a progressive-ratio schedule was not altered by intra-PPTg microinfusions of GABA agonists. These data confirm that the PPTg is involved in nicotine self-administration, a conclusion that is independent of the schedule of reinforcement that is used. GABAergic mechanisms in the PPTg play a selective role in nicotine reinforcement compared to cocaine, and that role is restricted to the characteristics of reinforcement measured by fixed-ratio responding.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>11702093</pmid><doi>10.1007/s002130100869</doi><tpages>8</tpages></addata></record>
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source MEDLINE; SpringerLink Journals - AutoHoldings
subjects Agonists
Animals
Baclofen
Biological and medical sciences
Brain Stem - drug effects
Brain Stem - physiology
Cocaine
Cocaine - administration & dosage
Dopamine Uptake Inhibitors - administration & dosage
Dose-Response Relationship, Drug
Drug self-administration
GABA Agonists - pharmacology
Glutamatergic transmission
Male
Medical sciences
Mesencephalon
Muscimol
Neurons
Nicotine
Nicotine - administration & dosage
Nicotinic Agonists - administration & dosage
pedunculopontine nucleus
Pedunculopontine tegmental nucleus
Rats
Rats, Long-Evans
Reinforcement Schedule
Reinforcement schedules
Self Administration
Tegmentum Mesencephali - drug effects
Tegmentum Mesencephali - physiology
Tobacco, tobacco smoking
Toxicology
γ-Aminobutyric acid
title GABA mechanisms in the pedunculopontine tegmental nucleus influence particular aspects of nicotine self-administration selectively in the rat
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