Elevated serotonin is involved in hyperactivity but not in the paradoxical effect of amphetamine in mice neonatally lesioned with 6-hydroxydopamine

The neonatal lesion with 6-hydroxydopamine (6-OHDA) in rodents induces juvenile hyperactivity and paradoxical hypolocomotor response to psychostimulants, in striking contrast to what is observed when similar lesions are carried out in adults. The early disruption of central dopaminergic pathways is...

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Publicado: 2004
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03604012_v78_n2_p289_Avale
http://hdl.handle.net/20.500.12110/paper_03604012_v78_n2_p289_Avale
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spelling paper:paper_03604012_v78_n2_p289_Avale2023-06-08T15:34:46Z Elevated serotonin is involved in hyperactivity but not in the paradoxical effect of amphetamine in mice neonatally lesioned with 6-hydroxydopamine 6-hydroxydopamine Dopamine p-chlorophenylalanine Serotonin amphetamine citalopram fenclonine oxidopamine psychostimulant agent serotonin serotonin transporter tritium tryptophan hydroxylase animal experiment animal model article autoradiography controlled study dopaminergic system drug effect female gene mutation hyperactivity male mouse nerve cell differentiation neurotransmission nonhuman phenotype priority journal serotoninergic system Amphetamine Animals Animals, Newborn Carrier Proteins Central Nervous System Stimulants Corpus Striatum Dopamine Dopamine Plasma Membrane Transport Proteins Fenclonine Male Membrane Glycoproteins Membrane Transport Proteins Mice Motor Activity Nerve Tissue Proteins Oxidopamine Serotonin Serotonin Plasma Membrane Transport Proteins Tryptophan Hydroxylase The neonatal lesion with 6-hydroxydopamine (6-OHDA) in rodents induces juvenile hyperactivity and paradoxical hypolocomotor response to psychostimulants, in striking contrast to what is observed when similar lesions are carried out in adults. The early disruption of central dopaminergic pathways is followed by increased striatal serotonin (5-HT) contents although the functional role of this neurodevelopmental adaptation remains unclear. The aim of the present study is to investigate the participation of this neurochemical imbalance in the main behavioral phenotypes of this model. To this end, mice received a neonatal administration of 6-OHDA that induced an 80% striatal dopamine depletion together with 70% increase in 5-HT. Serotoninergic hyperinnervation was evidenced further by increased [3H] citalopram autoradiographic binding and 5-HT transporter immunohistochemistry in striatal sections. To investigate whether elevated 5-HT was implicated in hyperactivity, we treated control and 6-OHDA neonatally lesioned mice with the selective irreversible tryptophan hydroxylase inhibitor p-chlorophenylalanine (PCPA) to induce 5-HT depletion. Normalization of striatal 5-HT in 6-OHDA neonatally lesioned mice to control levels reversed hyperactivity to normal locomotor scores, whereas the same extent of 5-HT depletion did not affect spontaneous locomotor activity of control mice. In turn, the paradoxical response to amphetamine in neonatal DA-depleted mice was not prevented by PCPA treatment. Taken together, our results suggest that the increased striatal 5-HT that follows neonatal DA depletion is involved in hyperlocomotor behavior but not in the paradoxical calming response to amphetamine observed in this mouse model. © 2004 Wiley-Liss, Inc. 2004 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03604012_v78_n2_p289_Avale http://hdl.handle.net/20.500.12110/paper_03604012_v78_n2_p289_Avale
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic 6-hydroxydopamine
Dopamine
p-chlorophenylalanine
Serotonin
amphetamine
citalopram
fenclonine
oxidopamine
psychostimulant agent
serotonin
serotonin transporter
tritium
tryptophan hydroxylase
animal experiment
animal model
article
autoradiography
controlled study
dopaminergic system
drug effect
female
gene mutation
hyperactivity
male
mouse
nerve cell differentiation
neurotransmission
nonhuman
phenotype
priority journal
serotoninergic system
Amphetamine
Animals
Animals, Newborn
Carrier Proteins
Central Nervous System Stimulants
Corpus Striatum
Dopamine
Dopamine Plasma Membrane Transport Proteins
Fenclonine
Male
Membrane Glycoproteins
Membrane Transport Proteins
Mice
Motor Activity
Nerve Tissue Proteins
Oxidopamine
Serotonin
Serotonin Plasma Membrane Transport Proteins
Tryptophan Hydroxylase
spellingShingle 6-hydroxydopamine
Dopamine
p-chlorophenylalanine
Serotonin
amphetamine
citalopram
fenclonine
oxidopamine
psychostimulant agent
serotonin
serotonin transporter
tritium
tryptophan hydroxylase
animal experiment
animal model
article
autoradiography
controlled study
dopaminergic system
drug effect
female
gene mutation
hyperactivity
male
mouse
nerve cell differentiation
neurotransmission
nonhuman
phenotype
priority journal
serotoninergic system
Amphetamine
Animals
Animals, Newborn
Carrier Proteins
Central Nervous System Stimulants
Corpus Striatum
Dopamine
Dopamine Plasma Membrane Transport Proteins
Fenclonine
Male
Membrane Glycoproteins
Membrane Transport Proteins
Mice
Motor Activity
Nerve Tissue Proteins
Oxidopamine
Serotonin
Serotonin Plasma Membrane Transport Proteins
Tryptophan Hydroxylase
Elevated serotonin is involved in hyperactivity but not in the paradoxical effect of amphetamine in mice neonatally lesioned with 6-hydroxydopamine
topic_facet 6-hydroxydopamine
Dopamine
p-chlorophenylalanine
Serotonin
amphetamine
citalopram
fenclonine
oxidopamine
psychostimulant agent
serotonin
serotonin transporter
tritium
tryptophan hydroxylase
animal experiment
animal model
article
autoradiography
controlled study
dopaminergic system
drug effect
female
gene mutation
hyperactivity
male
mouse
nerve cell differentiation
neurotransmission
nonhuman
phenotype
priority journal
serotoninergic system
Amphetamine
Animals
Animals, Newborn
Carrier Proteins
Central Nervous System Stimulants
Corpus Striatum
Dopamine
Dopamine Plasma Membrane Transport Proteins
Fenclonine
Male
Membrane Glycoproteins
Membrane Transport Proteins
Mice
Motor Activity
Nerve Tissue Proteins
Oxidopamine
Serotonin
Serotonin Plasma Membrane Transport Proteins
Tryptophan Hydroxylase
description The neonatal lesion with 6-hydroxydopamine (6-OHDA) in rodents induces juvenile hyperactivity and paradoxical hypolocomotor response to psychostimulants, in striking contrast to what is observed when similar lesions are carried out in adults. The early disruption of central dopaminergic pathways is followed by increased striatal serotonin (5-HT) contents although the functional role of this neurodevelopmental adaptation remains unclear. The aim of the present study is to investigate the participation of this neurochemical imbalance in the main behavioral phenotypes of this model. To this end, mice received a neonatal administration of 6-OHDA that induced an 80% striatal dopamine depletion together with 70% increase in 5-HT. Serotoninergic hyperinnervation was evidenced further by increased [3H] citalopram autoradiographic binding and 5-HT transporter immunohistochemistry in striatal sections. To investigate whether elevated 5-HT was implicated in hyperactivity, we treated control and 6-OHDA neonatally lesioned mice with the selective irreversible tryptophan hydroxylase inhibitor p-chlorophenylalanine (PCPA) to induce 5-HT depletion. Normalization of striatal 5-HT in 6-OHDA neonatally lesioned mice to control levels reversed hyperactivity to normal locomotor scores, whereas the same extent of 5-HT depletion did not affect spontaneous locomotor activity of control mice. In turn, the paradoxical response to amphetamine in neonatal DA-depleted mice was not prevented by PCPA treatment. Taken together, our results suggest that the increased striatal 5-HT that follows neonatal DA depletion is involved in hyperlocomotor behavior but not in the paradoxical calming response to amphetamine observed in this mouse model. © 2004 Wiley-Liss, Inc.
title Elevated serotonin is involved in hyperactivity but not in the paradoxical effect of amphetamine in mice neonatally lesioned with 6-hydroxydopamine
title_short Elevated serotonin is involved in hyperactivity but not in the paradoxical effect of amphetamine in mice neonatally lesioned with 6-hydroxydopamine
title_full Elevated serotonin is involved in hyperactivity but not in the paradoxical effect of amphetamine in mice neonatally lesioned with 6-hydroxydopamine
title_fullStr Elevated serotonin is involved in hyperactivity but not in the paradoxical effect of amphetamine in mice neonatally lesioned with 6-hydroxydopamine
title_full_unstemmed Elevated serotonin is involved in hyperactivity but not in the paradoxical effect of amphetamine in mice neonatally lesioned with 6-hydroxydopamine
title_sort elevated serotonin is involved in hyperactivity but not in the paradoxical effect of amphetamine in mice neonatally lesioned with 6-hydroxydopamine
publishDate 2004
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03604012_v78_n2_p289_Avale
http://hdl.handle.net/20.500.12110/paper_03604012_v78_n2_p289_Avale
_version_ 1768542693630148608