Identification of the GABAA receptor subtype mRNA in human pancreatic tissue

FEBS Lett. 1994 Jun 13;346(2-3):257-62. doi: 10.1016/0014-5793(94)00485-4.

Abstract

Evidence suggests a physiological role of the GABAA receptor in the pancreas. Clinically, an autoimmune reaction involving the GABA biosynthesizing enzyme, glutamic acid decarboxylase has been implicated in the development of insulin-dependent diabetes mellitus. To determine the subtypes of GABAA receptor expressed in human pancreas, we analyzed, with the use of the reverse-transcription/polymerase chain reaction technique human pancreatic tissue for the presence of GABAA receptor subunits alpha 1-6, beta 1-3, and gamma 1-2 transcripts. Unlike brain tissue, pancreatic tissue only expresses the alpha 2, beta 3 and gamma 1 subunits. Our results provide evidence of a specific GABAA receptor subtype expressed in human pancreatic tissue.

MeSH terms

  • Base Sequence
  • Benzodiazepines / pharmacology
  • Cerebral Cortex / chemistry
  • Cloning, Molecular
  • Drug Synergism
  • Humans
  • Macromolecular Substances
  • Molecular Sequence Data
  • Pancreas / chemistry*
  • Polymerase Chain Reaction
  • RNA / chemistry
  • RNA / genetics
  • RNA, Messenger / analysis*
  • RNA-Directed DNA Polymerase
  • Receptors, GABA / chemistry
  • Receptors, GABA / drug effects
  • Receptors, GABA / genetics*
  • Sequence Analysis
  • gamma-Aminobutyric Acid / pharmacology

Substances

  • Macromolecular Substances
  • RNA, Messenger
  • Receptors, GABA
  • Benzodiazepines
  • gamma-Aminobutyric Acid
  • RNA
  • RNA-Directed DNA Polymerase