Distinct electrophysiological properties of glutamatergic, cholinergic and GABAergic rat septohippocampal neurons: novel implications for hippocampal rhythmicity

J Physiol. 2003 Sep 15;551(Pt 3):927-43. doi: 10.1113/jphysiol.2003.046847. Epub 2003 Jul 15.

Abstract

The medial septum-diagonal band complex (MSDB) contains cholinergic and non-cholinergic neurons known to play key roles in learning and memory processing, and in the generation of hippocampal theta rhythm. Electrophysiologically, several classes of neurons have been described in the MSDB, but their chemical identity remains to be fully established. By combining electrophysiology with single-cell RT-PCR, we have identified four classes of neurons in the MSDB in vitro. The first class displayed slow-firing and little or no Ih, and expressed choline acetyl-transferase mRNA (ChAT). The second class was fast-firing, had a substantial Ih and expressed glutamic acid decarboxylase 67 mRNA (GAD67), sometimes co-localized with ChAT mRNAs. A third class exhibited fast- and burst-firing, had an important Ih and expressed GAD67 mRNA also occasionally co-localized with ChAT mRNAs. The ionic mechanism underlying the bursts involved a low-threshold spike and a prominent Ih current, conductances often associated with pacemaker activity. Interestingly, we identified a fourth class that expressed transcripts solely for one or two of the vesicular glutamate transporters (VGLUT1 and VGLUT2), but not ChAT or GAD. Some putative glutamatergic neurons displayed electrophysiological properties similar to ChAT-positive slow-firing neurons such as the occurrence of a very small Ih, but nearly half of glutamatergic neurons exhibited cluster firing with intrinsically generated voltage-dependent subthreshold membrane oscillations. Neurons belonging to each of the four described classes were found among septohippocampal neurons by retrograde labelling. We provide results suggesting that slow-firing cholinergic, fast-firing and burst-firing GABAergic, and cluster-firing glutamatergic neurons, may each uniquely contribute to hippocampal rhythmicity in vivo.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholine / physiology*
  • Action Potentials / drug effects
  • Action Potentials / physiology
  • Animals
  • Cardiotonic Agents / pharmacology
  • Carrier Proteins / genetics
  • Choline O-Acetyltransferase / genetics
  • Electrophysiology
  • Glutamate Decarboxylase / genetics
  • Glutamine / physiology*
  • Hippocampus / cytology
  • Hippocampus / physiology*
  • Isoenzymes / genetics
  • Membrane Transport Proteins*
  • Neurons / enzymology
  • Periodicity
  • Phenotype
  • Pyrimidines / pharmacology
  • RNA, Messenger / analysis
  • Rats
  • Rats, Sprague-Dawley
  • Septal Nuclei / cytology
  • Septal Nuclei / physiology*
  • Vesicular Glutamate Transport Protein 1
  • Vesicular Glutamate Transport Protein 2
  • Vesicular Transport Proteins*
  • gamma-Aminobutyric Acid / physiology*

Substances

  • Cardiotonic Agents
  • Carrier Proteins
  • Isoenzymes
  • Membrane Transport Proteins
  • Pyrimidines
  • RNA, Messenger
  • Slc17a6 protein, rat
  • Slc17a7 protein, rat
  • Vesicular Glutamate Transport Protein 1
  • Vesicular Glutamate Transport Protein 2
  • Vesicular Transport Proteins
  • Glutamine
  • ICI D2788
  • gamma-Aminobutyric Acid
  • Choline O-Acetyltransferase
  • Glutamate Decarboxylase
  • glutamate decarboxylase 1
  • Acetylcholine