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Arsenic-Induced Neurotoxicity by Dysfunctioning Cholinergic and Dopaminergic System in Brain of Developing Rats
by
Gupta, Richa
, Chandravanshi, Lalit P.
, Shukla, Rajendra K.
in
Acetylcholinesterase - metabolism
/ Animals
/ Arsenic
/ Arsenic - toxicity
/ Arsenites - toxicity
/ Biochemistry
/ Biomedical and Life Sciences
/ Biotechnology
/ Body weight
/ Brain
/ Brain - cytology
/ Brain - drug effects
/ Brain - metabolism
/ Cholinergic Neurons - drug effects
/ Cholinergic Neurons - metabolism
/ Chronic exposure
/ Cognition
/ Corpus striatum
/ Corpus Striatum - cytology
/ Corpus Striatum - drug effects
/ Corpus Striatum - metabolism
/ Cortex (frontal)
/ Dopamine
/ Dopamine D2 receptors
/ Dopaminergic Neurons - drug effects
/ Dopaminergic Neurons - metabolism
/ dose response
/ Drinking water
/ Exposure
/ Female
/ frontal lobe
/ Frontal Lobe - cytology
/ Frontal Lobe - drug effects
/ Frontal Lobe - metabolism
/ Gene expression
/ genes
/ Hippocampus
/ Hippocampus - cytology
/ Hippocampus - drug effects
/ Hippocampus - metabolism
/ Hydroxylase
/ Life Sciences
/ Male
/ memory
/ messenger RNA
/ Metabolites
/ mRNA
/ Neostriatum
/ Neurotoxicity
/ Nutrition
/ Oncology
/ Perinatal exposure
/ Pregnancy
/ Protein expression
/ Protein kinase C
/ protein synthesis
/ Proteins
/ Rats
/ Receptor, Muscarinic M2 - metabolism
/ RNA, Messenger
/ Sodium Compounds - toxicity
/ Spatial discrimination learning
/ spatial learning
/ Spatial Learning - drug effects
/ Spatial memory
/ Spatial Memory - drug effects
/ Tyrosine
/ Tyrosine 3-monooxygenase
2019
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Arsenic-Induced Neurotoxicity by Dysfunctioning Cholinergic and Dopaminergic System in Brain of Developing Rats
by
Gupta, Richa
, Chandravanshi, Lalit P.
, Shukla, Rajendra K.
in
Acetylcholinesterase - metabolism
/ Animals
/ Arsenic
/ Arsenic - toxicity
/ Arsenites - toxicity
/ Biochemistry
/ Biomedical and Life Sciences
/ Biotechnology
/ Body weight
/ Brain
/ Brain - cytology
/ Brain - drug effects
/ Brain - metabolism
/ Cholinergic Neurons - drug effects
/ Cholinergic Neurons - metabolism
/ Chronic exposure
/ Cognition
/ Corpus striatum
/ Corpus Striatum - cytology
/ Corpus Striatum - drug effects
/ Corpus Striatum - metabolism
/ Cortex (frontal)
/ Dopamine
/ Dopamine D2 receptors
/ Dopaminergic Neurons - drug effects
/ Dopaminergic Neurons - metabolism
/ dose response
/ Drinking water
/ Exposure
/ Female
/ frontal lobe
/ Frontal Lobe - cytology
/ Frontal Lobe - drug effects
/ Frontal Lobe - metabolism
/ Gene expression
/ genes
/ Hippocampus
/ Hippocampus - cytology
/ Hippocampus - drug effects
/ Hippocampus - metabolism
/ Hydroxylase
/ Life Sciences
/ Male
/ memory
/ messenger RNA
/ Metabolites
/ mRNA
/ Neostriatum
/ Neurotoxicity
/ Nutrition
/ Oncology
/ Perinatal exposure
/ Pregnancy
/ Protein expression
/ Protein kinase C
/ protein synthesis
/ Proteins
/ Rats
/ Receptor, Muscarinic M2 - metabolism
/ RNA, Messenger
/ Sodium Compounds - toxicity
/ Spatial discrimination learning
/ spatial learning
/ Spatial Learning - drug effects
/ Spatial memory
/ Spatial Memory - drug effects
/ Tyrosine
/ Tyrosine 3-monooxygenase
2019
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Arsenic-Induced Neurotoxicity by Dysfunctioning Cholinergic and Dopaminergic System in Brain of Developing Rats
by
Gupta, Richa
, Chandravanshi, Lalit P.
, Shukla, Rajendra K.
in
Acetylcholinesterase - metabolism
/ Animals
/ Arsenic
/ Arsenic - toxicity
/ Arsenites - toxicity
/ Biochemistry
/ Biomedical and Life Sciences
/ Biotechnology
/ Body weight
/ Brain
/ Brain - cytology
/ Brain - drug effects
/ Brain - metabolism
/ Cholinergic Neurons - drug effects
/ Cholinergic Neurons - metabolism
/ Chronic exposure
/ Cognition
/ Corpus striatum
/ Corpus Striatum - cytology
/ Corpus Striatum - drug effects
/ Corpus Striatum - metabolism
/ Cortex (frontal)
/ Dopamine
/ Dopamine D2 receptors
/ Dopaminergic Neurons - drug effects
/ Dopaminergic Neurons - metabolism
/ dose response
/ Drinking water
/ Exposure
/ Female
/ frontal lobe
/ Frontal Lobe - cytology
/ Frontal Lobe - drug effects
/ Frontal Lobe - metabolism
/ Gene expression
/ genes
/ Hippocampus
/ Hippocampus - cytology
/ Hippocampus - drug effects
/ Hippocampus - metabolism
/ Hydroxylase
/ Life Sciences
/ Male
/ memory
/ messenger RNA
/ Metabolites
/ mRNA
/ Neostriatum
/ Neurotoxicity
/ Nutrition
/ Oncology
/ Perinatal exposure
/ Pregnancy
/ Protein expression
/ Protein kinase C
/ protein synthesis
/ Proteins
/ Rats
/ Receptor, Muscarinic M2 - metabolism
/ RNA, Messenger
/ Sodium Compounds - toxicity
/ Spatial discrimination learning
/ spatial learning
/ Spatial Learning - drug effects
/ Spatial memory
/ Spatial Memory - drug effects
/ Tyrosine
/ Tyrosine 3-monooxygenase
2019
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Arsenic-Induced Neurotoxicity by Dysfunctioning Cholinergic and Dopaminergic System in Brain of Developing Rats
Journal Article
Arsenic-Induced Neurotoxicity by Dysfunctioning Cholinergic and Dopaminergic System in Brain of Developing Rats
2019
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Overview
Chronic exposure to arsenic via drinking water throughout the globe is assumed to cause a developmental neurotoxicity. Here, we investigated the effect of perinatal arsenic exposure on the neurobehavioral and neurochemical changes in the corpus striatum, frontal cortex, and hippocampus that is critically involved in motor and cognition functions. In continuation of previous studies, this study demonstrates that perinatal exposures (GD6–PD21) to arsenic (2 or 4 mg/kg body weight, p.o.) cause hypo-activity in arsenic-exposed rats on PD22. The hypo-activity was found to be linked with a decrease in the mRNA and protein expression of the DA-D2 receptor. Further, a protein expression of tyrosine hydroxylase (TH), levels of dopamine, and its metabolites were also significantly impaired in corpus striatum. The arsenic-exposed groups showed spatial learning and memory significantly below the average in a dose-dependent manner for the controls. Here, we evaluated the declined expression of CHRM2 receptor gene and protein expression of ChAT, PKCβ-1 in the frontal cortex and hippocampus, which are critically involved in cognition functions including learning and memory. A trend of recovery was found in the cholinergic and dopaminergic system of the brain, but changes remained persisted even after the withdrawal of arsenic exposure on PD45. Taken together, our results indicate that perinatal arsenic exposure appears to be critical and vulnerable as the development of cholinergic and dopaminergic system continues during this period.
Publisher
Springer US,Springer Nature B.V
Subject
Acetylcholinesterase - metabolism
/ Animals
/ Arsenic
/ Biomedical and Life Sciences
/ Brain
/ Cholinergic Neurons - drug effects
/ Cholinergic Neurons - metabolism
/ Corpus Striatum - drug effects
/ Corpus Striatum - metabolism
/ Dopamine
/ Dopaminergic Neurons - drug effects
/ Dopaminergic Neurons - metabolism
/ Exposure
/ Female
/ genes
/ Male
/ memory
/ mRNA
/ Oncology
/ Proteins
/ Rats
/ Receptor, Muscarinic M2 - metabolism
/ Spatial discrimination learning
/ Spatial Learning - drug effects
/ Spatial Memory - drug effects
/ Tyrosine
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