NYAS Conferences
New York Academy of Sciences
left end
Search
divider divider feedback right end
Annals of the New York Academy of Sciences Annals of the New York Academy of Sciences login

Main

Browse Volumes

Forthcoming Volumes

Annals PrePrints

Annals Extra

E-mail Alerts

Subscriptions & Orders

New Proposals

Author Guidelines

About Annals

Help

Get free Annals volume as a NYAS member: http://www.nyas.org/annalsreaderhw
Issue 1074 coverCellular and Molecular Mechanisms of Drugs of Abuse and Neurotoxicity Cocaine, GHB, and Substituted Amphetamines Volume 1074 published August 2006
Ann. N.Y. Acad. Sci. 1074: 13–30 (2006). doi: 10.1196/annals.1369.002
Copyright © 2006 by the New York Academy of Sciences
description | purchase volume purchase this volume

This Volume
Table of Contents
Description
This Article
Full Text
Full Text (PDF)
Services
Similar articles in this journal
Similar articles in PubMed
Alert me to new issues of the journal
Download to citation manager
Citing Articles
Citing Articles via Google Scholar
Google Scholar
Articles by CAI, N. S.
Articles by CADET, J. L.
Search for Related Content
PubMed
PubMed Citation
Articles by CAI, N. S.
Articles by CADET, J. L.

Serial Analysis of Gene Expression in the Rat Striatum Following Methamphetamine Administration

NING SHENG CAIa, MICHAEL T MCCOYa, BRUCE LADENHEIMa, JOHNALYN LYLESa, SYED F ALIb AND JEAN LUD CADETa

a Molecular Neuropsychiatry Branch, National Institute on Drug Abuse-Intramural Research Program, Baltimore, Maryland 21224, USA b Neurochemistry Laboratory, Division of Neurotoxicology, FDA/NCTR, Jefferson, Arkansas 72079, USA

Key Words: METH • SAGE • neurotoxicity • CHOP • carbonic anhydrase

Address for correspondence: Jean Lud Cadet, M.D., Molecular Neuropsychiatry Branch, National Institute on Drug Abuse, National Institute of Health, 5500 Nathan Shock Drive, Baltimore, MD 21224. Voice: 410-550-2953; fax: 410-550-2745.  e-mail: jcadet{at}intra.nida.nih.gov

Methamphetamine (METH), a highly addictive drug, can cause degeneration of monoaminergic terminals and neuronal apoptosis in the mammalian brain. In the present article, we have used serial analysis of gene expression (SAGE) to investigate patterns of gene expression in the striata of rats that were given a neurotoxic dose of the drug. SAGE libraries were generated from animals treated with either saline or METH (40 mg/kg) and sacrificed 2 h later. A total of 315 transcripts were differentially expressed between the two libraries (P < 0.05), with 179 (56%) being upregulated and 136 (44%) being downregulated by the METH injection. Of these, CAATT enhancer-binding protein homologous protein (CHOP)/GADD153 (growth arrest- and DNA damage-inducible gene 153) was found to be upregulated by about threefold. Analysis of the expression of genes downstream of CHOP (DOCs) revealed significant METH-induced increases in their expression. Because DOC1 is an analog of carbonic anhydrase (CA) which is involved in the interconversion between carbon dioxide and the bicarbonate ion, we also measured the effects of METH on the expression of several CAs. These were significantly upregulated by METH in a time-dependent fashion. These results indicate that METH toxicity is mediated, in part, by drug-induced perturbations of physiological processes that are dependent on normal pH and CO2 homeostasis.






footerLeft footerRight