Proteomic analysis reveals differentially expressed proteins in the rat frontal cortex after methamphetamine treatment

Metab Brain Dis. 2009 Dec;24(4):685-700. doi: 10.1007/s11011-009-9167-0. Epub 2009 Oct 14.

Abstract

Methamphetamine (MA) is an addictive psycho-stimulant and the illicit use of the drug is escalating. In the present study, we examined protein expression profiles in the rat frontal cortex exposed to a total of eight MA injections (1 mg/kg, intraperitoneal) using 2-DE based proteomics. We investigated protein changes occurring in both the cytosolic fraction and the membrane fraction. 2-DE analysis resulted in 62 cytosolic and 44 membrane protein spots that were differentially regulated in the frontal cortex of rats exposed to MA when compared to control animals. Of these spots, 47 cytosolic and 42 membrane proteins were identified respectively, using ESI-Quad-TOF, which included ubiquitin carboxyl-terminal hydrolase isozyme L1 (UCH-L1), beta-synuclein, 78 kDa glucose-regulated protein (GRP 78), gamma-enolase, dihydropyrimidase-related protein 2 (DRP 2), complexin 2 and synapsin II. These proteins are associated with protein degradation, redox regulation, energy metabolism, cellular growth, cytoskeletal modifications and synaptic function. Proteomic research may be useful in exploring the complex underlying molecular mechanisms of MA dependence.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Vesicular Transport / drug effects
  • Adaptor Proteins, Vesicular Transport / metabolism
  • Amphetamine-Related Disorders / metabolism*
  • Amphetamine-Related Disorders / physiopathology
  • Animals
  • Brain Chemistry / drug effects
  • Brain Chemistry / physiology
  • Cell Membrane / drug effects
  • Cell Membrane / metabolism
  • Cytosol / drug effects
  • Cytosol / metabolism
  • Disease Models, Animal
  • Dopamine Uptake Inhibitors / pharmacology
  • Heat-Shock Proteins / drug effects
  • Heat-Shock Proteins / metabolism
  • Intercellular Signaling Peptides and Proteins / metabolism
  • Male
  • Methamphetamine / pharmacology*
  • Nerve Tissue Proteins / drug effects*
  • Nerve Tissue Proteins / metabolism
  • Neuronal Plasticity / drug effects
  • Neuronal Plasticity / physiology
  • Phosphopyruvate Hydratase / drug effects
  • Phosphopyruvate Hydratase / metabolism
  • Prefrontal Cortex / drug effects*
  • Prefrontal Cortex / metabolism
  • Proteomics / methods
  • Rats
  • Rats, Sprague-Dawley
  • Synapsins / drug effects
  • Synapsins / metabolism
  • Synaptic Transmission / drug effects
  • Synaptic Transmission / physiology
  • Ubiquitin Thiolesterase / drug effects
  • Ubiquitin Thiolesterase / metabolism
  • beta-Synuclein / drug effects
  • beta-Synuclein / metabolism

Substances

  • Adaptor Proteins, Vesicular Transport
  • Dopamine Uptake Inhibitors
  • GRP78 protein, rat
  • Heat-Shock Proteins
  • Intercellular Signaling Peptides and Proteins
  • Nerve Tissue Proteins
  • Synapsins
  • Ubiquitin carboxyl-Terminal Hydrolase L-1, mouse
  • beta-Synuclein
  • collapsin response mediator protein-2
  • complexin II
  • Methamphetamine
  • Ubiquitin Thiolesterase
  • Phosphopyruvate Hydratase