ATP-induced inward current in neurons freshly dissociated from the tuberomammillary nucleus

J Neurophysiol. 1994 Mar;71(3):868-73. doi: 10.1152/jn.1994.71.3.868.

Abstract

1. Neurons in the tuberomammillary nucleus (TMN), which are considered to be histaminergic, were dissociated and their response to extracellularly applied ATP was investigated in the nystatin-perforated patch recording mode under voltage-clamp condition. 2. ATP induced a sustained inward current that was slowly desensitized at a holding potential of -60 mV. 3. The ATP response increased in a concentration-dependent manner. The half-maximum concentration (EC50) was 44 microM and the Hill coefficient was 1.8. 4. The potency of ATP analogues was in the order of ATP > or = 2-methylthio-ATP >> alpha, beta-methylene ATP > or = ADP. Neither adenosine nor AMP induced any response. The results suggest that the purinergic receptor in TMN neurons is P2y. 5. The current-voltage relationship for the 100 microM ATP showed a significant inward rectification at a potential more positive than -20 mV in an external solution with 150 mM Na+, but a significant rectification current was not observed in an external solution with 150 mM Cs+. The change in the reversal potential of the ATP response (EATP) to a 10-fold change of extracellular Na+ concentration was 56 mV, indicating that the ATP-induced current is highly selective for Na+ over Cl-. 6. The permeability ratio for cations was Na+:Li+:K+:Rb+: Cs+:Ca2+ = 2.16:1.36:1.68:1.54:1:2.55, indicating that the ATP-induced current is passing through the ligand-gated nonselective cation channel. 7. These results suggest that ATP has an excitatory effect on the TMN neurons by opening nonselective cation channels.

MeSH terms

  • Adenosine Triphosphate / physiology*
  • Animals
  • Calcium Channels / physiology
  • Chloride Channels / physiology
  • Histamine / physiology
  • Mammillary Bodies / physiology*
  • Neurons / physiology
  • Rats
  • Receptors, Purinergic P2 / physiology
  • Synaptic Transmission / physiology*

Substances

  • Calcium Channels
  • Chloride Channels
  • Receptors, Purinergic P2
  • Histamine
  • Adenosine Triphosphate