Evidence map›Paper›PMID 17913913›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2007

NMDA receptor contribution to the climbing fiber response in the adult mouse Purkinje cell.

Claire Piochon, Theano Irinopoulou, Daniel Brusciano, Yannick Bailly, Jean Mariani, Carole Levenes

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
3.0field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

68 citing papers in PubMed, 118 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. The calcium sensor, rather than the route of calcium entry, defines cerebellar plasticity pathways.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. α2δ-2 Protein Controls Structure and Function at the Cerebellar Climbing Fiber Synapse.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  20. Article

8 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 5 institutions in 1 country.

Claire PiochonUniversité Pierre et Marie Curie-Paris 6, Unité Mixte de Recherche 7102, Centre National de la Recherche Scientifique, Laboratoire Neurobiologie des Processus Adaptifs, Equipe Développement et Vieillissement du Système Nerveux, 75005 Paris, France.
Theano Irinopoulou
Daniel Brusciano
Yannick Bailly
Jean Mariani
Carole Levenes
Unit of Functional and Adaptive Biology · FRHôpital Charles-Foix · FRInserm · FRInstitut des Neurosciences Cellulaires et Intégratives · FRSorbonne Université · FR

Funding

CELL DEATH AND THE REGULATION OF PURKINJE CELL NUMBERR01NS034309 · NINDS · UNIVERSITY OF MARYLAND BALTIMORE · PI VOGEL, MICHAEL W · 1997 to 2004
$1.3M
NINDS NIH HHS NS34309NINDS NIH HHS R01 NS034309
6 · The paper itself

Abstract

Among integrative neurons displaying long-term synaptic plasticity, adult Purkinje cells seemed to be an exception by lacking functional NMDA receptors (NMDA-Rs). Although numerous anatomical studies have shown both NR1 and NR2 NMDA-R subunits in adult Purkinje cells, patch-clamp studies failed to detect any NMDA currents. Using more recent pharmacological and immunodetection tools, we demonstrate here that Purkinje cells from adult mice respond to exogenous NMDA application and that postsynaptic NMDA-Rs carry part of the climbing fiber-mediated EPSC (CF-EPSC), with undetectable contribution from presynaptic or polysynaptic NMDA currents. We also detect NR2-A/B subunits in adult Purkinje cells by immunohistochemistry. The NMDA-mediated CF-EPSC is barely detectable before 3 weeks postnatal. From the end of the third week, the number of cells displaying the NMDA-mediated CF-EPSC rapidly increases. Soon, this EPSC becomes detectable in all the Purkinje cells but is still very small. Its amplitude continues to increase until 12 weeks after birth. In mature Purkinje cells, we show that the NMDA-Rs contribute to the depolarizing plateau of complex spikes and increase their number of spikelets. Together, these observations demonstrate that mature Purkinje cells express functional NMDA receptors that become detectable in CF-EPSCs at approximately 21 d after birth and control the complex spike waveform.

Indexed as

Age FactorsAnimalsAnimals, NewbornCerebellumDrug InteractionsElectric StimulationExcitatory Amino Acid AgonistsExcitatory Amino Acid AntagonistsExcitatory Postsynaptic PotentialsIn Vitro TechniquesMiceMice, Inbred C57BLNerve FibersN-MethylaspartatePatch-Clamp TechniquesPurkinje CellsExcitatory Amino Acid AgonistsExcitatory Amino Acid AntagonistsN-MethylaspartateNR2A NMDA receptorReceptors, N-Methyl-D-Aspartate

Identifiers

PMID17913913
PMCPMC6672834
OpenAlexW1981032249

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.