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Age-related Effects of Heroin on Gene Expression in the Hippocampus and Striatum of Cynomolgus Monkeys

OBJECTIVE: The aim of this study was to investigate differentially expressed genes and their functions in the hippocampus and striatum after heroin administration in cynomolgus macaques of different ages. METHODS: Cynomolgus monkeys were divided by age as follows: 1 year (A1, n = 2); 3 to 4 years (A...

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Autores principales: Choi, Mi Ran, Jin, Yeung-Bae, Bang, Sol Hee, Im, Chang-Nim, Lee, Youngjeon, Kim, Han-Na, Chang, Kyu-Tae, Lee, Sang-Rae, Kim, Dai-Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean College of Neuropsychopharmacology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006971/
https://www.ncbi.nlm.nih.gov/pubmed/31958910
http://dx.doi.org/10.9758/cpn.2020.18.1.93
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author Choi, Mi Ran
Jin, Yeung-Bae
Bang, Sol Hee
Im, Chang-Nim
Lee, Youngjeon
Kim, Han-Na
Chang, Kyu-Tae
Lee, Sang-Rae
Kim, Dai-Jin
author_facet Choi, Mi Ran
Jin, Yeung-Bae
Bang, Sol Hee
Im, Chang-Nim
Lee, Youngjeon
Kim, Han-Na
Chang, Kyu-Tae
Lee, Sang-Rae
Kim, Dai-Jin
author_sort Choi, Mi Ran
collection PubMed
description OBJECTIVE: The aim of this study was to investigate differentially expressed genes and their functions in the hippocampus and striatum after heroin administration in cynomolgus macaques of different ages. METHODS: Cynomolgus monkeys were divided by age as follows: 1 year (A1, n = 2); 3 to 4 years (A2, n = 2); 6 to 8 years (A3, n = 2); and older than 11 years (A4, n = 2). After heroin was injected intramuscularly into the monkeys (0.6 mg/kg), we performed large-scale transcriptome profiling in the hippocampus (H) and striatum (S) using RNA sequencing technology. Some genes were validated with real-time quantitative PCR. RESULTS: In the hippocampus, the gene expression of A1H was similar to that of A4H, while the gene expression of A2H was similar to that of A3H. Genes associated with the mitogen-activated protein kinase signaling pathway (STMN1, FGF14, and MAPT) and γ-aminobutyric acid-ergic synapses (GABBR2 and GAD1) were differentially expressed among control and heroin-treated animals. Differential gene expression between A1S and A4S was the least significant, while differential gene expression between A3S and A2S was the most significant. Genes associated with the neurotrophin signaling pathway (NTRK1 and NGFR), autophagy (ATG5), and dopaminergic synapses (AKT1) in the striatum were differentially expressed among control and heroin-treated animals. CONCLUSION: These results suggest that even a single heroin exposure can cause differential gene expression in the hippocampus and striatum of nonhuman primates at different ages.
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spelling pubmed-70069712020-02-20 Age-related Effects of Heroin on Gene Expression in the Hippocampus and Striatum of Cynomolgus Monkeys Choi, Mi Ran Jin, Yeung-Bae Bang, Sol Hee Im, Chang-Nim Lee, Youngjeon Kim, Han-Na Chang, Kyu-Tae Lee, Sang-Rae Kim, Dai-Jin Clin Psychopharmacol Neurosci Original Article OBJECTIVE: The aim of this study was to investigate differentially expressed genes and their functions in the hippocampus and striatum after heroin administration in cynomolgus macaques of different ages. METHODS: Cynomolgus monkeys were divided by age as follows: 1 year (A1, n = 2); 3 to 4 years (A2, n = 2); 6 to 8 years (A3, n = 2); and older than 11 years (A4, n = 2). After heroin was injected intramuscularly into the monkeys (0.6 mg/kg), we performed large-scale transcriptome profiling in the hippocampus (H) and striatum (S) using RNA sequencing technology. Some genes were validated with real-time quantitative PCR. RESULTS: In the hippocampus, the gene expression of A1H was similar to that of A4H, while the gene expression of A2H was similar to that of A3H. Genes associated with the mitogen-activated protein kinase signaling pathway (STMN1, FGF14, and MAPT) and γ-aminobutyric acid-ergic synapses (GABBR2 and GAD1) were differentially expressed among control and heroin-treated animals. Differential gene expression between A1S and A4S was the least significant, while differential gene expression between A3S and A2S was the most significant. Genes associated with the neurotrophin signaling pathway (NTRK1 and NGFR), autophagy (ATG5), and dopaminergic synapses (AKT1) in the striatum were differentially expressed among control and heroin-treated animals. CONCLUSION: These results suggest that even a single heroin exposure can cause differential gene expression in the hippocampus and striatum of nonhuman primates at different ages. Korean College of Neuropsychopharmacology 2020-02 2020-02-29 /pmc/articles/PMC7006971/ /pubmed/31958910 http://dx.doi.org/10.9758/cpn.2020.18.1.93 Text en Copyright © 2020, Korean College of Neuropsychopharmacology This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Choi, Mi Ran
Jin, Yeung-Bae
Bang, Sol Hee
Im, Chang-Nim
Lee, Youngjeon
Kim, Han-Na
Chang, Kyu-Tae
Lee, Sang-Rae
Kim, Dai-Jin
Age-related Effects of Heroin on Gene Expression in the Hippocampus and Striatum of Cynomolgus Monkeys
title Age-related Effects of Heroin on Gene Expression in the Hippocampus and Striatum of Cynomolgus Monkeys
title_full Age-related Effects of Heroin on Gene Expression in the Hippocampus and Striatum of Cynomolgus Monkeys
title_fullStr Age-related Effects of Heroin on Gene Expression in the Hippocampus and Striatum of Cynomolgus Monkeys
title_full_unstemmed Age-related Effects of Heroin on Gene Expression in the Hippocampus and Striatum of Cynomolgus Monkeys
title_short Age-related Effects of Heroin on Gene Expression in the Hippocampus and Striatum of Cynomolgus Monkeys
title_sort age-related effects of heroin on gene expression in the hippocampus and striatum of cynomolgus monkeys
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006971/
https://www.ncbi.nlm.nih.gov/pubmed/31958910
http://dx.doi.org/10.9758/cpn.2020.18.1.93
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