Abstract
Substance abuse affects the central nervous system (CNS) and remains a global health problem. Psychostimulants, such as cocaine and methamphetamine (METH), and opioids affect neuronal function and lead to behavioral impairments via epigenetic modification. Epigenetic changes occur via classical pathways, especially the class III histone deacetylase (HDAC)-sirtuin (SIRT) family, that act as cellular sensors to regulate energy homeostasis and coordinate cellular responses to maintain genome integrity. However, SIRT family (1–7)-associated neurodegeneration has not been elucidated in the context of energy metabolism. The present study examined the effects of psychostimulants, such as cocaine and METH, and opioids, such as morphine, on SIRT family (1–7) [class I, II, III and IV] expression and cellular translocation-mediated dysfunction in astrocytes and microglial cells. The “nootropic” drug piracetam played a preventative role against psychostimulant- and opioid-induced SIRT (1–7) expression in astrocytes. These results indicate that cocaine, METH, and morphine affected deacetylation and cellular function, and these changes were prevented by piracetam in astrocytes.
Highlights
Substance abuse affects the central nervous system (CNS) and remains a global health problem
The present study investigated the effects of cocaine, METH- and morphine-mediated induction of SIRT (1–7) expression in astrocytes and microglia and analyzed the preventive effects of piracetam on psychostimulant- and opioid-induced SIRT expression in astrocytes
The present study determined whether the psychostimulant drugs cocaine and METH and the opioid morphine induced similar or distinct mechanisms of SIRT (1–7) expression in astrocytes and microglia
Summary
Substance abuse affects the central nervous system (CNS) and remains a global health problem Psychostimulants, such as cocaine and methamphetamine (METH), and opioids affect neuronal function and lead to behavioral impairments via epigenetic modification. The “nootropic” drug piracetam played a preventative role against psychostimulant- and opioid-induced SIRT (1–7) expression in astrocytes These results indicate that cocaine, METH, and morphine affected deacetylation and cellular function, and these changes were prevented by piracetam in astrocytes. Substance use disorder (SUD) causes 11.8 million annual deaths, and approximately 9.2% of Americans used illicit drugs, especially cocaine, methamphetamine (METH) and morphine, within the past m onth[1,2] These psychostimulants and opioids target several organs, including the central nervous system (CNS), and induce oxidative stress, reactive oxygen species (ROS) production, and metabolic dysfunction, including epigenetic modifications[3,4,5]. N AD+ is a central metabolic cofactor in eukaryotic cells that plays a critical role in regulating
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.