La maladie de Parkinson en France (serveur d'exploration)

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Levodopa : Is toxicity a myth?

Identifieur interne : 001619 ( PascalFrancis/Corpus ); précédent : 001618; suivant : 001620

Levodopa : Is toxicity a myth?

Auteurs : Y. Agid

Source :

RBID : Pascal:98-0231540

Descripteurs français

English descriptors

Abstract

Article abstract-Whether a drug such as levodopa, which is prescribed for long periods, may be toxic is a legitimate and even indispensable question. The problem is no different from that posed by other drugs-such as calcium antagonists, antihypertensives, or hormones-normally prescribed for chronic diseases. What, however, is meant in this context by "toxic" (from the Greek toxicon, meaning poison)? Irrevocable damage such as cell loss should not be confused with reversible side effects resulting from cell dysfunction. Clinically or experimentally, levodopa has not been shown to accelerate neurodegeneration or cause permanent impairment of cell function in a manner that would result in irreversible side effects. These data have been reasonably well established in vivo in animals and humans, although preliminary studies suggesting that levodopa is a trophic factor remain unconfirmed. Like oxygen or calcium, levodopa can be toxic in vitro when it is present in high concentrations or in the absence of glial cells. However, glial cells are much more numerous than neurons in vivo, so these conditions cannot simply be extrapolated to three-dimensional brain structures in which protective interactions with the cellular environment abound. Because levodopa remains the most effective treatment available for Parkinson's disease, questions regarding timing or manner of administration of the drug should arise not because levodopa is toxic to nerve cells, but because it causes reversible side effects. When the elementary rules of substitutive therapy to provide maximum comfort while limiting side effects are followed, we need not fear that levodopa is dangerous unless the contrary is proven.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

pA  
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A02 01      @0 NEURAI
A03   1    @0 Neurology
A05       @2 50
A06       @2 4
A08 01  1  ENG  @1 Levodopa : Is toxicity a myth?
A11 01  1    @1 AGID (Y.)
A14 01      @1 Federation de Neurologie and INSERM U289, Hôpital de la Salpetrière @2 Paris @3 FRA @Z 1 aut.
A20       @1 858-863
A21       @1 1998
A23 01      @0 ENG
A43 01      @1 INIST @2 6345 @5 354000075514280070
A44       @0 0000 @1 © 1998 INIST-CNRS. All rights reserved.
A45       @0 50 ref.
A47 01  1    @0 98-0231540
A60       @1 P
A61       @0 A
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C01 01    ENG  @0 Article abstract-Whether a drug such as levodopa, which is prescribed for long periods, may be toxic is a legitimate and even indispensable question. The problem is no different from that posed by other drugs-such as calcium antagonists, antihypertensives, or hormones-normally prescribed for chronic diseases. What, however, is meant in this context by "toxic" (from the Greek toxicon, meaning poison)? Irrevocable damage such as cell loss should not be confused with reversible side effects resulting from cell dysfunction. Clinically or experimentally, levodopa has not been shown to accelerate neurodegeneration or cause permanent impairment of cell function in a manner that would result in irreversible side effects. These data have been reasonably well established in vivo in animals and humans, although preliminary studies suggesting that levodopa is a trophic factor remain unconfirmed. Like oxygen or calcium, levodopa can be toxic in vitro when it is present in high concentrations or in the absence of glial cells. However, glial cells are much more numerous than neurons in vivo, so these conditions cannot simply be extrapolated to three-dimensional brain structures in which protective interactions with the cellular environment abound. Because levodopa remains the most effective treatment available for Parkinson's disease, questions regarding timing or manner of administration of the drug should arise not because levodopa is toxic to nerve cells, but because it causes reversible side effects. When the elementary rules of substitutive therapy to provide maximum comfort while limiting side effects are followed, we need not fear that levodopa is dangerous unless the contrary is proven.
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C03 04  X  SPA  @0 Neurona catecolaminérgica @5 07
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C07 02  X  FRE  @0 Système nerveux central pathologie @5 38
C07 02  X  ENG  @0 Central nervous system disease @5 38
C07 02  X  SPA  @0 Sistema nervosio central patología @5 38
C07 03  X  FRE  @0 Encéphale pathologie @5 39
C07 03  X  ENG  @0 Cerebral disorder @5 39
C07 03  X  SPA  @0 Encéfalo patología @5 39
C07 04  X  FRE  @0 Extrapyramidal syndrome @5 40
C07 04  X  ENG  @0 Extrapyramidal syndrome @5 40
C07 04  X  SPA  @0 Extrapiramidal síndrome @5 40
C07 05  X  FRE  @0 Maladie dégénérative @5 41
C07 05  X  ENG  @0 Degenerative disease @5 41
C07 05  X  SPA  @0 Enfermedad degenerativa @5 41
N21       @1 153

Format Inist (serveur)

NO : PASCAL 98-0231540 INIST
ET : Levodopa : Is toxicity a myth?
AU : AGID (Y.)
AF : Federation de Neurologie and INSERM U289, Hôpital de la Salpetrière/Paris/France (1 aut.)
DT : Publication en série; Niveau analytique
SO : Neurology; ISSN 0028-3878; Coden NEURAI; Etats-Unis; Da. 1998; Vol. 50; No. 4; Pp. 858-863; Bibl. 50 ref.
LA : Anglais
EA : Article abstract-Whether a drug such as levodopa, which is prescribed for long periods, may be toxic is a legitimate and even indispensable question. The problem is no different from that posed by other drugs-such as calcium antagonists, antihypertensives, or hormones-normally prescribed for chronic diseases. What, however, is meant in this context by "toxic" (from the Greek toxicon, meaning poison)? Irrevocable damage such as cell loss should not be confused with reversible side effects resulting from cell dysfunction. Clinically or experimentally, levodopa has not been shown to accelerate neurodegeneration or cause permanent impairment of cell function in a manner that would result in irreversible side effects. These data have been reasonably well established in vivo in animals and humans, although preliminary studies suggesting that levodopa is a trophic factor remain unconfirmed. Like oxygen or calcium, levodopa can be toxic in vitro when it is present in high concentrations or in the absence of glial cells. However, glial cells are much more numerous than neurons in vivo, so these conditions cannot simply be extrapolated to three-dimensional brain structures in which protective interactions with the cellular environment abound. Because levodopa remains the most effective treatment available for Parkinson's disease, questions regarding timing or manner of administration of the drug should arise not because levodopa is toxic to nerve cells, but because it causes reversible side effects. When the elementary rules of substitutive therapy to provide maximum comfort while limiting side effects are followed, we need not fear that levodopa is dangerous unless the contrary is proven.
CC : 002B02U01
FD : Parkinson maladie; Lévodopa; Antiparkinsonien; Neurone catécholaminergique; Noyau gris central; Article synthèse; Toxicité; Homme; Chimiothérapie
FG : Système nerveux pathologie; Système nerveux central pathologie; Encéphale pathologie; Extrapyramidal syndrome; Maladie dégénérative
ED : Parkinson disease; Levodopa; Antiparkinson agent; Catecholaminergic neuron; Basal ganglion; Review; Toxicity; Human; Chemotherapy
EG : Nervous system diseases; Central nervous system disease; Cerebral disorder; Extrapyramidal syndrome; Degenerative disease
GD : Giftigkeit
SD : Parkinson enfermedad; Levodopa; Antiparkinsoniano; Neurona catecolaminérgica; Núcleo basal; Artículo síntesis; Toxicidad; Hombre; Quimioterapia
LO : INIST-6345.354000075514280070
ID : 98-0231540

Links to Exploration step

Pascal:98-0231540

Le document en format XML

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<SO>Neurology; ISSN 0028-3878; Coden NEURAI; Etats-Unis; Da. 1998; Vol. 50; No. 4; Pp. 858-863; Bibl. 50 ref.</SO>
<LA>Anglais</LA>
<EA>Article abstract-Whether a drug such as levodopa, which is prescribed for long periods, may be toxic is a legitimate and even indispensable question. The problem is no different from that posed by other drugs-such as calcium antagonists, antihypertensives, or hormones-normally prescribed for chronic diseases. What, however, is meant in this context by "toxic" (from the Greek toxicon, meaning poison)? Irrevocable damage such as cell loss should not be confused with reversible side effects resulting from cell dysfunction. Clinically or experimentally, levodopa has not been shown to accelerate neurodegeneration or cause permanent impairment of cell function in a manner that would result in irreversible side effects. These data have been reasonably well established in vivo in animals and humans, although preliminary studies suggesting that levodopa is a trophic factor remain unconfirmed. Like oxygen or calcium, levodopa can be toxic in vitro when it is present in high concentrations or in the absence of glial cells. However, glial cells are much more numerous than neurons in vivo, so these conditions cannot simply be extrapolated to three-dimensional brain structures in which protective interactions with the cellular environment abound. Because levodopa remains the most effective treatment available for Parkinson's disease, questions regarding timing or manner of administration of the drug should arise not because levodopa is toxic to nerve cells, but because it causes reversible side effects. When the elementary rules of substitutive therapy to provide maximum comfort while limiting side effects are followed, we need not fear that levodopa is dangerous unless the contrary is proven.</EA>
<CC>002B02U01</CC>
<FD>Parkinson maladie; Lévodopa; Antiparkinsonien; Neurone catécholaminergique; Noyau gris central; Article synthèse; Toxicité; Homme; Chimiothérapie</FD>
<FG>Système nerveux pathologie; Système nerveux central pathologie; Encéphale pathologie; Extrapyramidal syndrome; Maladie dégénérative</FG>
<ED>Parkinson disease; Levodopa; Antiparkinson agent; Catecholaminergic neuron; Basal ganglion; Review; Toxicity; Human; Chemotherapy</ED>
<EG>Nervous system diseases; Central nervous system disease; Cerebral disorder; Extrapyramidal syndrome; Degenerative disease</EG>
<GD>Giftigkeit</GD>
<SD>Parkinson enfermedad; Levodopa; Antiparkinsoniano; Neurona catecolaminérgica; Núcleo basal; Artículo síntesis; Toxicidad; Hombre; Quimioterapia</SD>
<LO>INIST-6345.354000075514280070</LO>
<ID>98-0231540</ID>
</server>
</inist>
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