Alleviation of experimental hemiparkinsonism by high‐frequency stimulation of the subthalamic nucleus in primates: A comparison with L‐dopa treatment
Identifieur interne : 000602 ( France/Analysis ); précédent : 000601; suivant : 000603Alleviation of experimental hemiparkinsonism by high‐frequency stimulation of the subthalamic nucleus in primates: A comparison with L‐dopa treatment
Auteurs : Abdelhamid Benazzouz [France] ; Thomas Boraud [France] ; Jean Féger [France] ; Pierre Burbaud [France] ; Bernard Bioulac [France] ; Christian Gross [France]Source :
- Movement Disorders [ 0885-3185 ] ; 1996-11.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
- 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine, Akinesia, Aminoacid, Animal, Animals, Antiparkinson Agents (pharmacology), Antiparkinson agent, Comparative study, Dominance, Cerebral (drug effects), Dominance, Cerebral (physiology), Dopa, Electric, Electric Stimulation Therapy, Electromyography (drug effects), Experimental study, High frequency, High‐frequency stimulation, Instrumental stimulation, Levodopa (pharmacology), MPTP, Macaca mulatta, Motor Skills (drug effects), Motor Skills (physiology), Neurologic Examination (drug effects), Parkinson Disease, Secondary (chemically induced), Parkinson Disease, Secondary (physiopathology), Parkinsonism, Primates, Spasticity, Subthalamic nucleus, Thalamic Nuclei (drug effects), Thalamic Nuclei (physiopathology), Treatment, Unilateral.
- MESH :
- chemical , pharmacology : Antiparkinson Agents, Levodopa.
- chemical : 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine.
- chemically induced : Parkinson Disease, Secondary.
- drug effects : Dominance, Cerebral, Electromyography, Motor Skills, Neurologic Examination, Thalamic Nuclei.
- physiology : Dominance, Cerebral, Motor Skills.
- physiopathology : Parkinson Disease, Secondary, Thalamic Nuclei.
- Animals, Electric Stimulation Therapy, Macaca mulatta.
Abstract
Experimental studies in 1‐methyl‐4‐phenyl‐1,2,3,6‐tetrahydropyridine (MPTP)‐treated monkeys have shown that akinesia and rigidity are linked to a hyperactivity of glutamatergic subthalamic nucleus neurons and that the lesion of this nucleus can ameliorate parkinsonian motor signs. In our study, high‐frequency stimulation applied at the subthalamic level was performed on two Macaca mulatta monkeys rendered hemiparkinsonian by unilateral infusion of MPTP. Its effects on rigidity and bradykinesia have been quantified. The results exhibit an important alleviation of both symptoms during the application of subthalamic stimulation comparable to that obtained during L‐Dopa treatment, but without the appearance of abnormal movements such hemiballism or dyskinesia. Our data show that subthalamic stimulation has a beneficial effect on experimental parkinsonian rigidity and bradykinesia and suggests a new therapy approach for the treatment of Parkinson's disease by using subthalamic high‐frequency stimulation instead of L‐Dopa treatment.
Url:
DOI: 10.1002/mds.870110606
Affiliations:
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Disord.</title><idno type="ISSN">0885-3185</idno><idno type="eISSN">1531-8257</idno><imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>Hoboken</pubPlace><date type="published" when="1996-11">1996-11</date><biblScope unit="vol">11</biblScope><biblScope unit="issue">6</biblScope><biblScope unit="page" from="627">627</biblScope><biblScope unit="page" to="632">632</biblScope></imprint><idno type="ISSN">0885-3185</idno></series><idno type="istex">AA534287B555AF33E66A45B2FEB19234D8573FB5</idno><idno type="DOI">10.1002/mds.870110606</idno><idno type="ArticleID">MDS870110606</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0885-3185</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine</term><term>Akinesia</term><term>Aminoacid</term><term>Animal</term><term>Animals</term><term>Antiparkinson Agents (pharmacology)</term><term>Antiparkinson agent</term><term>Comparative study</term><term>Dominance, Cerebral (drug effects)</term><term>Dominance, Cerebral (physiology)</term><term>Dopa</term><term>Electric</term><term>Electric Stimulation Therapy</term><term>Electromyography (drug effects)</term><term>Experimental study</term><term>High frequency</term><term>High‐frequency stimulation</term><term>Instrumental stimulation</term><term>Levodopa (pharmacology)</term><term>MPTP</term><term>Macaca mulatta</term><term>Motor Skills (drug effects)</term><term>Motor Skills (physiology)</term><term>Neurologic Examination (drug effects)</term><term>Parkinson Disease, Secondary (chemically induced)</term><term>Parkinson Disease, Secondary (physiopathology)</term><term>Parkinsonism</term><term>Primates</term><term>Spasticity</term><term>Subthalamic nucleus</term><term>Thalamic Nuclei (drug effects)</term><term>Thalamic Nuclei (physiopathology)</term><term>Treatment</term><term>Unilateral</term></keywords><keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Antiparkinson Agents</term><term>Levodopa</term></keywords><keywords scheme="MESH" type="chemical" xml:lang="en"><term>1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine</term></keywords><keywords scheme="MESH" qualifier="chemically induced" xml:lang="en"><term>Parkinson Disease, Secondary</term></keywords><keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Dominance, Cerebral</term><term>Electromyography</term><term>Motor Skills</term><term>Neurologic Examination</term><term>Thalamic Nuclei</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Dominance, Cerebral</term><term>Motor Skills</term></keywords><keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Parkinson Disease, Secondary</term><term>Thalamic Nuclei</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Animals</term><term>Electric Stimulation Therapy</term><term>Macaca mulatta</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Akinésie</term><term>Aminoacide</term><term>Animal</term><term>Antiparkinsonien</term><term>Dopa</term><term>Electrique</term><term>Etude comparative</term><term>Etude expérimentale</term><term>Haute fréquence</term><term>Hypertonie spastique</term><term>Noyau sousthalamique</term><term>Parkinsonisme</term><term>Primates</term><term>Stimulation instrumentale</term><term>Traitement</term><term>Unilatéral</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Experimental studies in 1‐methyl‐4‐phenyl‐1,2,3,6‐tetrahydropyridine (MPTP)‐treated monkeys have shown that akinesia and rigidity are linked to a hyperactivity of glutamatergic subthalamic nucleus neurons and that the lesion of this nucleus can ameliorate parkinsonian motor signs. In our study, high‐frequency stimulation applied at the subthalamic level was performed on two Macaca mulatta monkeys rendered hemiparkinsonian by unilateral infusion of MPTP. Its effects on rigidity and bradykinesia have been quantified. The results exhibit an important alleviation of both symptoms during the application of subthalamic stimulation comparable to that obtained during L‐Dopa treatment, but without the appearance of abnormal movements such hemiballism or dyskinesia. Our data show that subthalamic stimulation has a beneficial effect on experimental parkinsonian rigidity and bradykinesia and suggests a new therapy approach for the treatment of Parkinson's disease by using subthalamic high‐frequency stimulation instead of L‐Dopa treatment.</div></front></TEI><affiliations><list><country><li>France</li></country><settlement><li>Bordeaux</li><li>Paris</li></settlement></list><tree><country name="France"><noRegion><name sortKey="Benazzouz, Abdelhamid" sort="Benazzouz, Abdelhamid" uniqKey="Benazzouz A" first="Abdelhamid" last="Benazzouz">Abdelhamid Benazzouz</name></noRegion><name sortKey="Bioulac, Bernard" sort="Bioulac, Bernard" uniqKey="Bioulac B" first="Bernard" last="Bioulac">Bernard Bioulac</name><name sortKey="Boraud, Thomas" sort="Boraud, Thomas" uniqKey="Boraud T" first="Thomas" last="Boraud">Thomas Boraud</name><name sortKey="Burbaud, Pierre" sort="Burbaud, Pierre" uniqKey="Burbaud P" first="Pierre" last="Burbaud">Pierre Burbaud</name><name sortKey="Feger, Jean" sort="Feger, Jean" uniqKey="Feger J" first="Jean" last="Féger">Jean Féger</name><name sortKey="Gross, Christian" sort="Gross, Christian" uniqKey="Gross C" first="Christian" last="Gross">Christian Gross</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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