The VMAT2 gene in mice and humans: amphetamine responses, locomotion, cardiac arrhythmias, aging, and vulnerability to dopaminergic toxins

FASEB J. 2000 Dec;14(15):2459-65. doi: 10.1096/fj.00-0205rev.

Abstract

Monoamine compartmentalization in monoaminergic neurons uses serial action of the plasma membrane and vesicular monoamine (VAMT2) transporters. We can now define the sequences of the genes encoding these transporters in mice and humans, examine influences of deletions of this gene and alteration in its expression levels in transgenic mice, and identify sequence polymorphisms in the human VMAT2 gene. Examination of VMAT2 variants can provide potential insights into roles for allelic variants at these loci in variant drug responses and in diseases linked to monoaminergic systems, including substance abuse and Parkinson's disease.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Aging / genetics
  • Amphetamines / pharmacology
  • Animals
  • Arrhythmias, Cardiac / genetics
  • Humans
  • MPTP Poisoning / genetics
  • Membrane Glycoproteins / genetics*
  • Membrane Transport Proteins*
  • Mice
  • Neuropeptides*
  • Polymorphism, Genetic
  • Rats
  • Vesicular Biogenic Amine Transport Proteins
  • Vesicular Monoamine Transport Proteins

Substances

  • Amphetamines
  • Membrane Glycoproteins
  • Membrane Transport Proteins
  • Neuropeptides
  • SLC18A2 protein, human
  • Slc18a2 protein, mouse
  • Slc18a2 protein, rat
  • Vesicular Biogenic Amine Transport Proteins
  • Vesicular Monoamine Transport Proteins