The dopamine transporter: A crucial component regulating dopamine transmission
Identifieur interne : 008268 ( Main/Merge ); précédent : 008267; suivant : 008269The dopamine transporter: A crucial component regulating dopamine transmission
Auteurs : Mohamed Jaber [États-Unis, France] ; Sara Jones [États-Unis] ; Bruno Giros [États-Unis] ; Caron [États-Unis]Source :
- Movement Disorders [ 0885-3185 ] ; 1997-09.
Descripteurs français
- Wicri :
- topic : Toxicomanie.
English descriptors
- KwdEn :
- Amphetamines (pharmacology), Animals, Brain, Brain (metabolism), Carrier Proteins (genetics), Carrier Proteins (physiology), Central Nervous System Stimulants (pharmacology), Cocaine (pharmacology), Disease Models, Animal, Dopamine (metabolism), Dopamine Plasma Membrane Transport Proteins, Dopamine Uptake Inhibitors (pharmacology), Dopamine transmission, Dopamine transporter, Drug addiction, Gene Dosage, Gene knockout procedure, Genotype, Homeostasis (genetics), Homeostasis (physiology), Humans, Hyperkinesis (chemically induced), Hyperkinesis (genetics), Hyperkinesis (physiopathology), Membrane Glycoproteins (genetics), Membrane Glycoproteins (physiology), Membrane Transport Proteins, Mice, Mice, Knockout, Mice, Transgenic, Nerve Tissue Proteins, Parkinson Disease (physiopathology), Parkinson's disease, Phenotype, Rats, Schizophrenia, Schizophrenia (drug therapy), Schizophrenia (physiopathology), Substance-Related Disorders (physiopathology).
- MESH :
- chemical , genetics : Carrier Proteins, Membrane Glycoproteins.
- chemical , metabolism : Dopamine.
- chemical , pharmacology : Amphetamines, Central Nervous System Stimulants, Cocaine, Dopamine Uptake Inhibitors.
- chemical , physiology : Carrier Proteins, Homeostasis, Membrane Glycoproteins.
- chemically induced : Hyperkinesis.
- drug therapy : Schizophrenia.
- genetics : Homeostasis, Hyperkinesis.
- metabolism : Brain.
- physiopathology : Hyperkinesis, Parkinson Disease, Schizophrenia, Substance-Related Disorders.
- Animals, Disease Models, Animal, Dopamine Plasma Membrane Transport Proteins, Gene Dosage, Genotype, Humans, Membrane Transport Proteins, Mice, Mice, Knockout, Mice, Transgenic, Nerve Tissue Proteins, Phenotype, Rats.
Abstract
The dopamine system is implicated in the control of locomotion, cognition, and endocrine function, The relative contribution of the various dopamine‐related components is not well established mainly because drugs that target the dopaminergic system often lack selectivity. The in vivo gene inactivation procedure, or knockout, enables the creation of new strains of mice lacking a specific gene. This technique has been applied recently to inactivate the expression of the plasma membrane dopamine transporter. Here we summarize the main findings obtained with these transgenic mice carrying this “genetic defect.” leading to a better understanding of the relative contribution of the dopamine transporter regarding locomotor activity, regulation of the expression of peptides under the control of dopaminergic activity, and responses to various drugs targeting the dopamine system. Our results establish not only the central importance of the transporter as the key element controlling dopamine levels in the brain, but also its role as an obligatory target for the behavioral and biochemical action of amphetamine and cocaine. In addition, the genetically altered mice offer a unique model to test the specificity and selectivity of dopamine transporter‐acting drugs and may provide important new concepts related to the clinical and social implications of conditions such as Parkinson's disease, schizophrenia, and drug addiction.
Url:
DOI: 10.1002/mds.870120502
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<front><div type="abstract" xml:lang="en">The dopamine system is implicated in the control of locomotion, cognition, and endocrine function, The relative contribution of the various dopamine‐related components is not well established mainly because drugs that target the dopaminergic system often lack selectivity. The in vivo gene inactivation procedure, or knockout, enables the creation of new strains of mice lacking a specific gene. This technique has been applied recently to inactivate the expression of the plasma membrane dopamine transporter. Here we summarize the main findings obtained with these transgenic mice carrying this “genetic defect.” leading to a better understanding of the relative contribution of the dopamine transporter regarding locomotor activity, regulation of the expression of peptides under the control of dopaminergic activity, and responses to various drugs targeting the dopamine system. Our results establish not only the central importance of the transporter as the key element controlling dopamine levels in the brain, but also its role as an obligatory target for the behavioral and biochemical action of amphetamine and cocaine. In addition, the genetically altered mice offer a unique model to test the specificity and selectivity of dopamine transporter‐acting drugs and may provide important new concepts related to the clinical and social implications of conditions such as Parkinson's disease, schizophrenia, and drug addiction.</div>
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<front><div type="abstract" xml:lang="en">The dopamine system is implicated in the control of locomotion, cognition, and endocrine function, The relative contribution of the various dopamine‐related components is not well established mainly because drugs that target the dopaminergic system often lack selectivity. The in vivo gene inactivation procedure, or knockout, enables the creation of new strains of mice lacking a specific gene. This technique has been applied recently to inactivate the expression of the plasma membrane dopamine transporter. Here we summarize the main findings obtained with these transgenic mice carrying this “genetic defect.” leading to a better understanding of the relative contribution of the dopamine transporter regarding locomotor activity, regulation of the expression of peptides under the control of dopaminergic activity, and responses to various drugs targeting the dopamine system. Our results establish not only the central importance of the transporter as the key element controlling dopamine levels in the brain, but also its role as an obligatory target for the behavioral and biochemical action of amphetamine and cocaine. In addition, the genetically altered mice offer a unique model to test the specificity and selectivity of dopamine transporter‐acting drugs and may provide important new concepts related to the clinical and social implications of conditions such as Parkinson's disease, schizophrenia, and drug addiction.</div>
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<term>Phenotype</term>
<term>Rats</term>
<term>Schizophrenia (drug therapy)</term>
<term>Schizophrenia (physiopathology)</term>
<term>Substance-Related Disorders (physiopathology)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Carrier Proteins</term>
<term>Membrane Glycoproteins</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Dopamine</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Amphetamines</term>
<term>Central Nervous System Stimulants</term>
<term>Cocaine</term>
<term>Dopamine Uptake Inhibitors</term>
</keywords>
<keywords scheme="MESH" qualifier="chemically induced" xml:lang="en"><term>Hyperkinesis</term>
</keywords>
<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en"><term>Schizophrenia</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Homeostasis</term>
<term>Hyperkinesis</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Brain</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="physiology" xml:lang="en"><term>Carrier Proteins</term>
<term>Homeostasis</term>
<term>Membrane Glycoproteins</term>
</keywords>
<keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Hyperkinesis</term>
<term>Parkinson Disease</term>
<term>Schizophrenia</term>
<term>Substance-Related Disorders</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Animals</term>
<term>Disease Models, Animal</term>
<term>Dopamine Plasma Membrane Transport Proteins</term>
<term>Gene Dosage</term>
<term>Genotype</term>
<term>Humans</term>
<term>Membrane Transport Proteins</term>
<term>Mice</term>
<term>Mice, Knockout</term>
<term>Mice, Transgenic</term>
<term>Nerve Tissue Proteins</term>
<term>Phenotype</term>
<term>Rats</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">The dopamine system is implicated in the control of locomotion, cognition, and endocrine function. The relative contribution of the various dopamine-related components is not well established mainly because drugs that target the dopaminergic system often lack selectivity. The in vivo gene inactivation procedure, or knockout, enables the creation of new strains of mice lacking a specific gene. This technique has been applied recently to inactivate the expression of the plasma membrane dopamine transporter. Here we summarize the main findings obtained with these transgenic mice carrying this "genetic defect," leading to a better understanding of the relative contribution of the dopamine transporter regarding locomotor activity, regulation of the expression of peptides under the control of dopaminergic activity, and responses to various drugs targeting the dopamine system. Our results establish not only the central importance of the transporter as the key element controlling dopamine levels in the brain, but also its role as an obligatory target for the behavioral and biochemical action of amphetamine and cocaine. In addition, the genetically altered mice offer a unique model to test the specificity and selectivity of dopamine transporter-acting drugs and may provide important new concepts related to the clinical and social implications of conditions such as Parkinson's disease, schizophrenia, and drug addiction.</div>
</front>
</TEI>
</PubMed>
</double>
</record>
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