Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Excitatory synaptic currents in Purkinje cells.

D J Perkel1, S Hestrin, P Sah

  • 1Department of Physiology, University of California, San Francisco 94143-0444.

Proceedings. Biological Sciences
|August 22, 1990
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

The Balance Hypothesis for the Avian Lumbosacral Organ and an Exploration of Its Morphological Variation.

Integrative organismal biology (Oxford, England)·2021
Same author

Evidence for newly generated interneurons in the basolateral amygdala of adult mice.

Molecular psychiatry·2017
Same author

Fibrillar structure of cellulose of bacterial and animal origin.

Nature·2010
Same author

Differentiation between glucose, galactose and mannose by a colour reaction.

Nature·2010
Same author

Climate change and the integrity of science.

Science (New York, N.Y.)·2010
Same author

Phosphorylase activity in human endometrium.

American journal of obstetrics and gynecology·2010

Adult rat Purkinje cells exclusively use non-N-methyl-D-aspartate (NMDA) receptors for excitatory synaptic transmission. Both climbing-fibre and parallel-fibre inputs rely solely on these non-NMDA receptors, indicating a lack of NMDA receptor involvement in these cerebellar circuits.

Area of Science:

  • Neuroscience
  • Molecular Biology
  • Cellular Physiology

Background:

  • Glutamate receptors, including N-methyl-D-aspartate (NMDA) and non-NMDA types, mediate excitatory synaptic transmission in the central nervous system.
  • Non-NMDA receptors are crucial for basal synaptic transmission, while NMDA receptors are involved in synaptic plasticity and depolarization.
  • Understanding the specific glutamate receptor subtypes in cerebellar Purkinje cells is vital for comprehending cerebellar function.

Purpose of the Study:

  • To elucidate the types of glutamate receptors responsible for excitatory synaptic transmission onto Purkinje cells in the adult rat cerebellum.
  • To differentiate the roles of NMDA and non-NMDA receptors in synaptic responses evoked by climbing-fibre and parallel-fibre stimulation.

Main Methods:

  • Whole-cell patch-clamp recordings were performed on Purkinje cells in adult rat cerebellar slices.

Related Experiment Videos

  • Excitatory postsynaptic currents (EPSCs) were elicited by stimulating climbing fibres (white matter/granule-cell layer) and parallel fibres (molecular layer).
  • Pharmacological analysis using NMDA receptor antagonist APV and non-NMDA receptor antagonist CNQX, along with current-voltage (I-V) relationship assessments.
  • Main Results:

    • Parallel-fibre stimulation induced a facilitated EPSC, while climbing-fibre stimulation resulted in a depressed EPSC upon paired-pulse stimulation.
    • Both parallel-fibre and climbing-fibre EPSCs showed linear I-V relationships and were insensitive to APV but blocked by CNQX.
    • Application of NMDA did not evoke a current, whereas glutamate/aspartate induced currents were significantly reduced by CNQX, confirming non-NMDA receptor mediation.

    Conclusions:

    • Excitatory synaptic transmission to adult Purkinje cells is exclusively mediated by non-NMDA type glutamate receptors.
    • Purkinje cells in adult rats appear to entirely lack functional NMDA receptors for these excitatory inputs.
    • These findings clarify the specific glutamatergic receptor composition underlying cerebellar excitatory synaptic transmission.