Electrophysiological characteristics of cells in the anterior caudal lobe of the mormyrid cerebellum

Neuroscience. 2010 Nov 24;171(1):79-91. doi: 10.1016/j.neuroscience.2010.08.033. Epub 2010 Aug 21.

Abstract

We have examined the basic electrophysiology and pharmacology of cells in the anterior caudal lobe (CLa) of the mormyrid cerebellum. Intracellular recordings were performed in an in vitro slice preparation using the whole-cell patch recording method. The responses of cells to parallel fiber (PF) and climbing fiber (CF) stimulation and to somatic current injection were recorded, and then characterized by bath application of receptor and ion channel blockers. Using biocytin or neurobiotin, these cells were also morphologically identified after recording to ensure their classification. Efferent cells and two subtypes of Purkinje cells were identified on the basis of their physiology and morphology. While the majority of Purkinje cells fire a single type of spike that is mediated by Na(+), some fire a large broad spike mediated by Ca(2+) and a narrow spike mediated by Na(+) at resting potential levels. By patching one recording electrode to the soma and another to one of the proximal dendrites of the same cell simultaneously, it was found that the Na(+) spike has an axonal origin and the Ca(2+) spike is generated in the soma-dendritic region of Purkinje cells. Efferent cells fire a single type of Na(+) spike only. Despite variations in their physiology and morphology, all cell types responded to PF stimulation with graded excitatory postsynaptic potentials (EPSPs) mediated by AMPA receptors. However, none of the efferent cells and only some of the Purkinje cells responded to CF activation with a large, AMPA receptor-mediated all-or-none EPSPs. We conclude that the functional circuitry of the CLa resembles that of other regions of the mormyrid cerebellum and is largely similar to that of the mammalian cerebellum.

Publication types

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

MeSH terms

  • 6-Cyano-7-nitroquinoxaline-2,3-dione / pharmacology
  • Animals
  • Axons / drug effects
  • Biophysics
  • Cerebellum / cytology*
  • Dendrites / drug effects
  • Dose-Response Relationship, Drug
  • Electric Fish / anatomy & histology*
  • Electric Stimulation
  • Excitatory Amino Acid Agonists / pharmacology
  • Excitatory Amino Acid Antagonists / pharmacology
  • Excitatory Postsynaptic Potentials / drug effects
  • Excitatory Postsynaptic Potentials / physiology
  • In Vitro Techniques
  • Lysine / analogs & derivatives
  • Lysine / metabolism
  • Membrane Potentials / drug effects
  • Membrane Potentials / physiology*
  • Mice
  • N-Methylaspartate / pharmacology
  • Nerve Fibers / physiology
  • Patch-Clamp Techniques
  • Purkinje Cells / cytology
  • Purkinje Cells / drug effects
  • Purkinje Cells / physiology*
  • Sodium Channel Blockers / pharmacology
  • Tetrodotoxin / pharmacology

Substances

  • Excitatory Amino Acid Agonists
  • Excitatory Amino Acid Antagonists
  • Sodium Channel Blockers
  • Tetrodotoxin
  • N-Methylaspartate
  • 6-Cyano-7-nitroquinoxaline-2,3-dione
  • biocytin
  • Lysine