𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Amphetamine effects on brain protein structure and oxidative stress as revealed by FTIR microspectroscopy

✍ Scribed by A. Rodríguez-Casado; I. Alvarez; A. Toledano; E. de Miguel; P. Carmona


Book ID
101723184
Publisher
Wiley (John Wiley & Sons)
Year
2007
Tongue
English
Weight
250 KB
Volume
86
Category
Article
ISSN
0006-3525

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Amphetamines are psychostimulants abused by man, that eventually leads to drug dependence. Amphetamine administration to rodents has been shown to provoke significant neurotoxicity involving dopaminergic nerve terminal degeneration. However, little information related to the effect of amphetamines on reactive oxygen species (ROS) production and neurotoxicity in brain is currently available. Herein we report the biochemical alterations of lipids and proteins in brain sections from amphetamine‐treated rodents using infrared microspectroscopy, immunohistochemistry, and immunoblotting. The spectroscopic changes reveal for the first time the formation of β‐sheet‐rich proteins in the cortex, but no significant protein alterations are visible in hippocampus region where hydroperoxide concentration is found to be lower relative to cortex. These result suggest that ROS generated by amphetamine‐mediated oxidative stress induce formation β‐sheet‐rich proteins which can be of amyloid β‐like character. © 2007 Wiley Periodicals, Inc. Biopolymers 86: 437–446, 2007.

This article was originally published online as an accepted preprint. The “Published Online” date corresponds to the preprint version. You can request a copy of the preprint by emailing the Biopolymers editorial office at [email protected]


📜 SIMILAR VOLUMES


FTIR microspectroscopic analysis of the
✍ P. Carmona; A. Rodríguez-Casado; I. Alvarez; E. de Miguel; A. Toledano 📂 Article 📅 2008 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 119 KB

## Abstract This study reports the changes in lipids and proteins of different brain areas of nicotine, D(+)‐amphetamine, and nicotine and D(+)‐amphetamine treated rats by monitoring lipid peroxidation and protein β‐sheet formation using infrared microspectroscopy. Compared with the untreated brain