In vivo characterization of the angiotensin-(1-7)-induced dopamine and gamma-aminobutyric acid release in the striatum of the rat

Eur J Neurosci. 2005 Aug;22(3):658-64. doi: 10.1111/j.1460-9568.2005.04188.x.

Abstract

The effect of angiotensin (Ang)-1-7 on dopamine, gamma-aminobutyric acid (GABA) and glutamate release in the striatum of the rat was examined using in vivo microdialysis. Ang-(1-7) was administered locally in the striatum through the microdialysis probe. At a concentration of 100 microm, Ang-(1-7) caused a significant increase in extracellular dopamine and GABA but had no effect on glutamate release. The Ang-(1-7)-induced dopamine release was blocked by EC33, an inhibitor of aminopeptidase A, an enzyme which converts Ang-(1-7) into Ang-(3-7), suggesting that this effect occurs after metabolism into Ang-(3-7). Indeed, administration of Ang-(3-7) (10-100 microm) into the striatum caused a more potent increase in the striatal dopamine release than Ang-(1-7). Because Ang-(3-7) is an inhibitor of insulin-regulated aminopeptidase (IRAP) and because Ang IV, another IRAP inhibitor, also causes a concentration-dependent increase in dopamine in the rat striatum, IRAP may be involved in this effect. In contrast, EC33 had no effect on the Ang-(1-7)-induced GABA increase but the GABA release was blocked by the putative AT(1-7) receptor antagonist A779 (0.1 microm) and by the nitric oxide synthase inhibitor L-NAME (1 mm). These drugs could not block the effect of Ang-(1-7) on the striatal dopamine release suggesting that only the observed effects on GABA release are mediated by the AT(1-7) receptor and/or are associated with a release of nitric oxide.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiotensin I / pharmacology*
  • Angiotensin II / analogs & derivatives
  • Angiotensin II / pharmacology
  • Angiotensin II Type 1 Receptor Blockers / pharmacology
  • Animals
  • Benzimidazoles / pharmacology
  • Biphenyl Compounds
  • Chromatography / methods
  • Corpus Striatum / drug effects*
  • Corpus Striatum / metabolism
  • Dopamine / metabolism*
  • Dose-Response Relationship, Drug
  • Drug Interactions
  • Enzyme Inhibitors / pharmacology
  • Imidazoles / pharmacology
  • Male
  • Microdialysis / methods
  • NG-Nitroarginine Methyl Ester / pharmacology
  • Peptide Fragments / pharmacology*
  • Pyridines / pharmacology
  • Rats
  • Rats, Wistar
  • Sulfonic Acids / pharmacology
  • Tetrazoles / pharmacology
  • Time Factors
  • gamma-Aminobutyric Acid / metabolism*

Substances

  • 7-Ala-angiotensin (1-7)
  • Angiotensin II Type 1 Receptor Blockers
  • Benzimidazoles
  • Biphenyl Compounds
  • EC 33
  • Enzyme Inhibitors
  • Imidazoles
  • Peptide Fragments
  • Pyridines
  • Sulfonic Acids
  • Tetrazoles
  • Angiotensin II
  • PD 123319
  • gamma-Aminobutyric Acid
  • Angiotensin I
  • angiotensin I (1-7)
  • candesartan
  • NG-Nitroarginine Methyl Ester
  • Dopamine