Combined Effects of Simultaneous Exposure to Caffeine and Cocaine in the Mouse Striatum

Caffeine is the world’s most popular psychoactive drug and is also an active adulterant found in many drugs of abuse, including seized cocaine samples. Despite several studies which examine the effects of caffeine or cocaine administered as single agents, little data are available for these agents w...

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Publicado: 2016
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_10298428_v29_n4_p525_Muniz
http://hdl.handle.net/20.500.12110/paper_10298428_v29_n4_p525_Muniz
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spelling paper:paper_10298428_v29_n4_p525_Muniz2023-06-08T16:00:21Z Combined Effects of Simultaneous Exposure to Caffeine and Cocaine in the Mouse Striatum Astroglia Caffeine Cocaine Dopamine Locomotor sensitization Striatum adenosine A2a receptor alpha amino 3 hydroxy 5 methyl 4 isoxazolepropionic acid caffeine cocaine dopamine 1 receptor dopamine 2 receptor glial fibrillary acidic protein glutamate receptor messenger RNA n methyl dextro aspartic acid caffeine central stimulant agent cocaine dopamine uptake inhibitor drug combination glial fibrillary acidic protein membrane protein messenger RNA nerve protein animal experiment animal tissue Article astrocytosis brain function controlled study corpus striatum down regulation gene expression genetic analysis immunohistochemistry immunoreactivity locomotion maladjustment male mouse nerve cell plasticity nonhuman priority journal sensitization upregulation analysis of variance animal C57BL mouse corpus striatum drug combination drug effects gene expression regulation genetics metabolism time factor Analysis of Variance Animals Caffeine Central Nervous System Stimulants Cocaine Corpus Striatum Dopamine Uptake Inhibitors Drug Combinations Gene Expression Regulation Glial Fibrillary Acidic Protein Locomotion Male Membrane Proteins Mice Mice, Inbred C57BL Nerve Tissue Proteins RNA, Messenger Time Factors Caffeine is the world’s most popular psychoactive drug and is also an active adulterant found in many drugs of abuse, including seized cocaine samples. Despite several studies which examine the effects of caffeine or cocaine administered as single agents, little data are available for these agents when given in combination. The purpose of the present study was to determine if combined intake of both psychostimulants can lead to maladaptive changes in striatal function. Mice were injected with a binge regimen (intermittent treatment for 13 days) of caffeine (3 × 5 mg/kg), cocaine (3 × 10 mg/kg), or combined administration. We found that chronic caffeine potentiated locomotion induced by cocaine and that both caffeine-treated groups showed sensitization. Striatal tissue was obtained 24 h and 7 days after last injection (withdrawal) for immunohistochemistry and mRNA expression. Our results show that combined intake of both psychostimulants can increase GFAP immunoreactivity in the striatum at both times post treatment. Gene expression analysis, targeted at dopamine, adenosine, and glutamate receptor subunit genes, revealed significant transcript down-regulation in the dorsal striatum of AMPA, NMDA, D1 and D2 receptor subunit mRNA expression in the group that received combined treatment, but not after individual administration. At withdrawal, we found increased D1 receptor mRNA expression along with increased A1, AMPA, NMDA, and metabotropic subunit expression. A2A mRNA showed decreased expression after both times in all experimental groups. Our study provides evidence that there are striatal alterations mediated by combined caffeine and cocaine administration, and highlights negative outcomes of chronic intake of both psychostimulants. © 2016, Springer Science+Business Media New York. 2016 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_10298428_v29_n4_p525_Muniz http://hdl.handle.net/20.500.12110/paper_10298428_v29_n4_p525_Muniz
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Astroglia
Caffeine
Cocaine
Dopamine
Locomotor sensitization
Striatum
adenosine A2a receptor
alpha amino 3 hydroxy 5 methyl 4 isoxazolepropionic acid
caffeine
cocaine
dopamine 1 receptor
dopamine 2 receptor
glial fibrillary acidic protein
glutamate receptor
messenger RNA
n methyl dextro aspartic acid
caffeine
central stimulant agent
cocaine
dopamine uptake inhibitor
drug combination
glial fibrillary acidic protein
membrane protein
messenger RNA
nerve protein
animal experiment
animal tissue
Article
astrocytosis
brain function
controlled study
corpus striatum
down regulation
gene expression
genetic analysis
immunohistochemistry
immunoreactivity
locomotion
maladjustment
male
mouse
nerve cell plasticity
nonhuman
priority journal
sensitization
upregulation
analysis of variance
animal
C57BL mouse
corpus striatum
drug combination
drug effects
gene expression regulation
genetics
metabolism
time factor
Analysis of Variance
Animals
Caffeine
Central Nervous System Stimulants
Cocaine
Corpus Striatum
Dopamine Uptake Inhibitors
Drug Combinations
Gene Expression Regulation
Glial Fibrillary Acidic Protein
Locomotion
Male
Membrane Proteins
Mice
Mice, Inbred C57BL
Nerve Tissue Proteins
RNA, Messenger
Time Factors
spellingShingle Astroglia
Caffeine
Cocaine
Dopamine
Locomotor sensitization
Striatum
adenosine A2a receptor
alpha amino 3 hydroxy 5 methyl 4 isoxazolepropionic acid
caffeine
cocaine
dopamine 1 receptor
dopamine 2 receptor
glial fibrillary acidic protein
glutamate receptor
messenger RNA
n methyl dextro aspartic acid
caffeine
central stimulant agent
cocaine
dopamine uptake inhibitor
drug combination
glial fibrillary acidic protein
membrane protein
messenger RNA
nerve protein
animal experiment
animal tissue
Article
astrocytosis
brain function
controlled study
corpus striatum
down regulation
gene expression
genetic analysis
immunohistochemistry
immunoreactivity
locomotion
maladjustment
male
mouse
nerve cell plasticity
nonhuman
priority journal
sensitization
upregulation
analysis of variance
animal
C57BL mouse
corpus striatum
drug combination
drug effects
gene expression regulation
genetics
metabolism
time factor
Analysis of Variance
Animals
Caffeine
Central Nervous System Stimulants
Cocaine
Corpus Striatum
Dopamine Uptake Inhibitors
Drug Combinations
Gene Expression Regulation
Glial Fibrillary Acidic Protein
Locomotion
Male
Membrane Proteins
Mice
Mice, Inbred C57BL
Nerve Tissue Proteins
RNA, Messenger
Time Factors
Combined Effects of Simultaneous Exposure to Caffeine and Cocaine in the Mouse Striatum
topic_facet Astroglia
Caffeine
Cocaine
Dopamine
Locomotor sensitization
Striatum
adenosine A2a receptor
alpha amino 3 hydroxy 5 methyl 4 isoxazolepropionic acid
caffeine
cocaine
dopamine 1 receptor
dopamine 2 receptor
glial fibrillary acidic protein
glutamate receptor
messenger RNA
n methyl dextro aspartic acid
caffeine
central stimulant agent
cocaine
dopamine uptake inhibitor
drug combination
glial fibrillary acidic protein
membrane protein
messenger RNA
nerve protein
animal experiment
animal tissue
Article
astrocytosis
brain function
controlled study
corpus striatum
down regulation
gene expression
genetic analysis
immunohistochemistry
immunoreactivity
locomotion
maladjustment
male
mouse
nerve cell plasticity
nonhuman
priority journal
sensitization
upregulation
analysis of variance
animal
C57BL mouse
corpus striatum
drug combination
drug effects
gene expression regulation
genetics
metabolism
time factor
Analysis of Variance
Animals
Caffeine
Central Nervous System Stimulants
Cocaine
Corpus Striatum
Dopamine Uptake Inhibitors
Drug Combinations
Gene Expression Regulation
Glial Fibrillary Acidic Protein
Locomotion
Male
Membrane Proteins
Mice
Mice, Inbred C57BL
Nerve Tissue Proteins
RNA, Messenger
Time Factors
description Caffeine is the world’s most popular psychoactive drug and is also an active adulterant found in many drugs of abuse, including seized cocaine samples. Despite several studies which examine the effects of caffeine or cocaine administered as single agents, little data are available for these agents when given in combination. The purpose of the present study was to determine if combined intake of both psychostimulants can lead to maladaptive changes in striatal function. Mice were injected with a binge regimen (intermittent treatment for 13 days) of caffeine (3 × 5 mg/kg), cocaine (3 × 10 mg/kg), or combined administration. We found that chronic caffeine potentiated locomotion induced by cocaine and that both caffeine-treated groups showed sensitization. Striatal tissue was obtained 24 h and 7 days after last injection (withdrawal) for immunohistochemistry and mRNA expression. Our results show that combined intake of both psychostimulants can increase GFAP immunoreactivity in the striatum at both times post treatment. Gene expression analysis, targeted at dopamine, adenosine, and glutamate receptor subunit genes, revealed significant transcript down-regulation in the dorsal striatum of AMPA, NMDA, D1 and D2 receptor subunit mRNA expression in the group that received combined treatment, but not after individual administration. At withdrawal, we found increased D1 receptor mRNA expression along with increased A1, AMPA, NMDA, and metabotropic subunit expression. A2A mRNA showed decreased expression after both times in all experimental groups. Our study provides evidence that there are striatal alterations mediated by combined caffeine and cocaine administration, and highlights negative outcomes of chronic intake of both psychostimulants. © 2016, Springer Science+Business Media New York.
title Combined Effects of Simultaneous Exposure to Caffeine and Cocaine in the Mouse Striatum
title_short Combined Effects of Simultaneous Exposure to Caffeine and Cocaine in the Mouse Striatum
title_full Combined Effects of Simultaneous Exposure to Caffeine and Cocaine in the Mouse Striatum
title_fullStr Combined Effects of Simultaneous Exposure to Caffeine and Cocaine in the Mouse Striatum
title_full_unstemmed Combined Effects of Simultaneous Exposure to Caffeine and Cocaine in the Mouse Striatum
title_sort combined effects of simultaneous exposure to caffeine and cocaine in the mouse striatum
publishDate 2016
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_10298428_v29_n4_p525_Muniz
http://hdl.handle.net/20.500.12110/paper_10298428_v29_n4_p525_Muniz
_version_ 1768542326240575488