Activity-dependent reduction of dopamine D2 receptors during a postnatal critical period of plasticity in rat striatum is not affected by prenatal haloperidol treatment

Motor activity induced in the Circling Training test (CT) during a postnatal (PN) critical period of plasticity (PN30-37) produces a long-lasting decrease in the number of binding sites and mRNA expression levels of the dopamine D2 receptor (D2R) in rat striatum. Prenatal exposure to the antipsychot...

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Autores principales: Soiza Reilly, Mariano, Azcurra, Julio Marcos
Publicado: 2011
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rat
Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_07365748_v29_n8_p855_SoizaReilly
http://hdl.handle.net/20.500.12110/paper_07365748_v29_n8_p855_SoizaReilly
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spelling paper:paper_07365748_v29_n8_p855_SoizaReilly2023-06-08T15:44:11Z Activity-dependent reduction of dopamine D2 receptors during a postnatal critical period of plasticity in rat striatum is not affected by prenatal haloperidol treatment Soiza Reilly, Mariano Azcurra, Julio Marcos Critical period of plasticity Development Dopamine D2 receptor Haloperidol Motor behavior Striatum dopamine 2 receptor haloperidol messenger RNA sodium chloride adulthood animal experiment animal tissue article binding site controlled study corpus striatum female gene expression gestation period instrumental conditioning learning male motor activity nerve cell plasticity nonhuman ontogeny perinatal period prenatal drug exposure priority journal progeny pup (rodent) rat receptor binding Animals Behavior, Animal Binding Sites Corpus Striatum Dopamine Dopamine Antagonists Female Fetus Gestational Age Haloperidol Humans Male Motor Activity Neuronal Plasticity Pregnancy Prenatal Exposure Delayed Effects Random Allocation Rats Rats, Sprague-Dawley Receptors, Dopamine D2 RNA, Messenger Animalia Rattus Motor activity induced in the Circling Training test (CT) during a postnatal (PN) critical period of plasticity (PN30-37) produces a long-lasting decrease in the number of binding sites and mRNA expression levels of the dopamine D2 receptor (D2R) in rat striatum. Prenatal exposure to the antipsychotic haloperidol also decreases postnatal levels of the striatal D2R in the offspring. We examined whether such fetal exposure to haloperidol could affect the activity-dependent reduction of the D2R system during the critical period. Half of the male offspring exposed to either haloperidol (2.5. mg/kg/day), i.p.) or saline during gestational days 5-18 were subjected to the CT during the critical period, while the remaining represented CT control animals. The adult number of binding sites and mRNA expression levels of the striatal D2R at PN90 were not changed by prenatal haloperidol treatment alone. On the other hand, only pups subjected to the CT during the critical period showed decreases in both studied parameters, regardless the prenatal treatment. These findings indicated that the postnatal reduction of the striatal D2R binding induced prenatally by haloperidol does not affect long-lasting activity-dependent plastic changes on the same receptor system elicited by motor activity in an ontogenetic critical period of plasticity in rat striatum. © 2011 ISDN. Fil:Soiza-Reilly, M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Azcurra, J.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2011 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_07365748_v29_n8_p855_SoizaReilly http://hdl.handle.net/20.500.12110/paper_07365748_v29_n8_p855_SoizaReilly
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Critical period of plasticity
Development
Dopamine D2 receptor
Haloperidol
Motor behavior
Striatum
dopamine 2 receptor
haloperidol
messenger RNA
sodium chloride
adulthood
animal experiment
animal tissue
article
binding site
controlled study
corpus striatum
female
gene expression
gestation period
instrumental conditioning
learning
male
motor activity
nerve cell plasticity
nonhuman
ontogeny
perinatal period
prenatal drug exposure
priority journal
progeny
pup (rodent)
rat
receptor binding
Animals
Behavior, Animal
Binding Sites
Corpus Striatum
Dopamine
Dopamine Antagonists
Female
Fetus
Gestational Age
Haloperidol
Humans
Male
Motor Activity
Neuronal Plasticity
Pregnancy
Prenatal Exposure Delayed Effects
Random Allocation
Rats
Rats, Sprague-Dawley
Receptors, Dopamine D2
RNA, Messenger
Animalia
Rattus
spellingShingle Critical period of plasticity
Development
Dopamine D2 receptor
Haloperidol
Motor behavior
Striatum
dopamine 2 receptor
haloperidol
messenger RNA
sodium chloride
adulthood
animal experiment
animal tissue
article
binding site
controlled study
corpus striatum
female
gene expression
gestation period
instrumental conditioning
learning
male
motor activity
nerve cell plasticity
nonhuman
ontogeny
perinatal period
prenatal drug exposure
priority journal
progeny
pup (rodent)
rat
receptor binding
Animals
Behavior, Animal
Binding Sites
Corpus Striatum
Dopamine
Dopamine Antagonists
Female
Fetus
Gestational Age
Haloperidol
Humans
Male
Motor Activity
Neuronal Plasticity
Pregnancy
Prenatal Exposure Delayed Effects
Random Allocation
Rats
Rats, Sprague-Dawley
Receptors, Dopamine D2
RNA, Messenger
Animalia
Rattus
Soiza Reilly, Mariano
Azcurra, Julio Marcos
Activity-dependent reduction of dopamine D2 receptors during a postnatal critical period of plasticity in rat striatum is not affected by prenatal haloperidol treatment
topic_facet Critical period of plasticity
Development
Dopamine D2 receptor
Haloperidol
Motor behavior
Striatum
dopamine 2 receptor
haloperidol
messenger RNA
sodium chloride
adulthood
animal experiment
animal tissue
article
binding site
controlled study
corpus striatum
female
gene expression
gestation period
instrumental conditioning
learning
male
motor activity
nerve cell plasticity
nonhuman
ontogeny
perinatal period
prenatal drug exposure
priority journal
progeny
pup (rodent)
rat
receptor binding
Animals
Behavior, Animal
Binding Sites
Corpus Striatum
Dopamine
Dopamine Antagonists
Female
Fetus
Gestational Age
Haloperidol
Humans
Male
Motor Activity
Neuronal Plasticity
Pregnancy
Prenatal Exposure Delayed Effects
Random Allocation
Rats
Rats, Sprague-Dawley
Receptors, Dopamine D2
RNA, Messenger
Animalia
Rattus
description Motor activity induced in the Circling Training test (CT) during a postnatal (PN) critical period of plasticity (PN30-37) produces a long-lasting decrease in the number of binding sites and mRNA expression levels of the dopamine D2 receptor (D2R) in rat striatum. Prenatal exposure to the antipsychotic haloperidol also decreases postnatal levels of the striatal D2R in the offspring. We examined whether such fetal exposure to haloperidol could affect the activity-dependent reduction of the D2R system during the critical period. Half of the male offspring exposed to either haloperidol (2.5. mg/kg/day), i.p.) or saline during gestational days 5-18 were subjected to the CT during the critical period, while the remaining represented CT control animals. The adult number of binding sites and mRNA expression levels of the striatal D2R at PN90 were not changed by prenatal haloperidol treatment alone. On the other hand, only pups subjected to the CT during the critical period showed decreases in both studied parameters, regardless the prenatal treatment. These findings indicated that the postnatal reduction of the striatal D2R binding induced prenatally by haloperidol does not affect long-lasting activity-dependent plastic changes on the same receptor system elicited by motor activity in an ontogenetic critical period of plasticity in rat striatum. © 2011 ISDN.
author Soiza Reilly, Mariano
Azcurra, Julio Marcos
author_facet Soiza Reilly, Mariano
Azcurra, Julio Marcos
author_sort Soiza Reilly, Mariano
title Activity-dependent reduction of dopamine D2 receptors during a postnatal critical period of plasticity in rat striatum is not affected by prenatal haloperidol treatment
title_short Activity-dependent reduction of dopamine D2 receptors during a postnatal critical period of plasticity in rat striatum is not affected by prenatal haloperidol treatment
title_full Activity-dependent reduction of dopamine D2 receptors during a postnatal critical period of plasticity in rat striatum is not affected by prenatal haloperidol treatment
title_fullStr Activity-dependent reduction of dopamine D2 receptors during a postnatal critical period of plasticity in rat striatum is not affected by prenatal haloperidol treatment
title_full_unstemmed Activity-dependent reduction of dopamine D2 receptors during a postnatal critical period of plasticity in rat striatum is not affected by prenatal haloperidol treatment
title_sort activity-dependent reduction of dopamine d2 receptors during a postnatal critical period of plasticity in rat striatum is not affected by prenatal haloperidol treatment
publishDate 2011
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_07365748_v29_n8_p855_SoizaReilly
http://hdl.handle.net/20.500.12110/paper_07365748_v29_n8_p855_SoizaReilly
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AT azcurrajuliomarcos activitydependentreductionofdopamined2receptorsduringapostnatalcriticalperiodofplasticityinratstriatumisnotaffectedbyprenatalhaloperidoltreatment
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