Pertussis toxin treatment prevents 5-HT(5a) receptor-mediated inhibition of cyclic AMP accumulation in rat C6 glioma cells

J Neurosci Res. 2000 Jul 1;61(1):75-81. doi: 10.1002/1097-4547(20000701)61:1<75::AID-JNR9>3.0.CO;2-9.

Abstract

We have investigated the functional coupling of the rat 5HT(5a) receptor subtype to adenylate cyclase in a rat C6 glioma cell line. In 5HT(5a) receptor-transfected cells, 5HT caused a concentration-dependent inhibition of forskolin-stimulated cAMP accumulation, with an EC(50) value of 41 nM and a maximal effect of 57% inhibition. This effect was dependent on the concentration of forskolin used to elevate cAMP levels. Methiothepin (1 mcM), which has high affinity for the 5HT(5a) receptor, antagonized the 5HT(5a) receptor-mediated inhibition, and unmasked a stimulation of cAMP formation similar to that observed in untransfected cells, whereas ketanserin (0.1 mcM) enhanced the inhibitory effect of 5HT. Pertussis toxin treatment (0.5 mcg/ml) completely blocked the inhibitory effect of 5HT on cAMP formation, also revealing increase in cAMP accumulation. Pretreatment of the transfected membranes with pertussis toxin abolished subsequent ADP-ribosylation of a 41 kDa protein, correlating the cAMP effect with a functional uncoupling of an inhibitory G protein from its receptor. These results demonstrate an efficient functional coupling of the rat 5HT(5a) receptor to the inhibition of adenylate cyclase via a pertussis toxin-sensitive G[alpha(i)], inhibitory G-protein.

Publication types

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

MeSH terms

  • Adenosine Diphosphate Ribose / metabolism
  • Adenylate Cyclase Toxin*
  • Adenylyl Cyclases / metabolism
  • Animals
  • Colforsin / pharmacology
  • Cyclic AMP / metabolism*
  • GTP-Binding Protein alpha Subunits, Gi-Go / metabolism
  • Gene Expression / physiology
  • Glioma
  • Ketanserin / pharmacology
  • Neurons / cytology
  • Neurons / enzymology
  • Pertussis Toxin*
  • Protein Structure, Tertiary
  • Rats
  • Receptors, Serotonin / chemistry
  • Receptors, Serotonin / genetics
  • Receptors, Serotonin / metabolism*
  • Serotonin / metabolism
  • Serotonin Antagonists / pharmacology
  • Transfection
  • Tumor Cells, Cultured
  • Virulence Factors, Bordetella / pharmacology*

Substances

  • Adenylate Cyclase Toxin
  • Receptors, Serotonin
  • Serotonin Antagonists
  • Virulence Factors, Bordetella
  • serotonin 5 receptor
  • Colforsin
  • Adenosine Diphosphate Ribose
  • Serotonin
  • Ketanserin
  • Cyclic AMP
  • Pertussis Toxin
  • GTP-Binding Protein alpha Subunits, Gi-Go
  • Adenylyl Cyclases