Evidence map›Paper›PMID 8755602›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1996

Starburst amacrine cells change from spiking to nonspiking neurons during retinal development.

Z J Zhou, G L Fain

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
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

21 citing papers in PubMed.

  1. Review
  2. Article
  3. Colour and melanopsin mediated responses in the murine retina.Frontiers in cellular neuroscience · 2023
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Disruption and recovery of patterned retinal activity in the absence of acetylcholine.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2005
    Article
  18. A unique role for Kv3 voltage-gated potassium channels in starburst amacrine cell signaling in mouse retina.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2004
    Article
  19. Spontaneous activity in developing turtle retinal ganglion cells: pharmacological studies.The Journal of neuroscience : the official journal of the Society for Neuroscience · 1999
    Article
  20. Retinal waves are governed by collective network properties.The Journal of neuroscience : the official journal of the Society for Neuroscience · 1999
    Article
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

2 authors.

Z J ZhouDepartment of Physiological Science, University of California, Los Angeles 90024-1527, USA.
G L Fain

Funding

PHYSIOLOGY OF PHOTORECEPTORSR01EY001844 · NEI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI GORDON Lee FAIN · 1985 to 2026
$9.9M
PHYSIOLOGY OF THE VERTEBRATE RETINAR01EY010894 · NEI · YALE UNIVERSITY · PI ZHOU, Z JIMMY · 1995 to 2011
$3.8M
NEI NIH HHS R01 EY01844NEI NIH HHS R01EY10894
6 · The paper itself

Abstract

The membrane excitability of cholinergic (starburst) amacrine cells was studied in the rabbit retina during postnatal development. Whole-cell patch-clamp recordings were made from 110 displaced starburst cells in a thin retina] slice preparation of rabbits between postnatal days P1 and P56 old. We report that displaced starburst cells undergo a dramatic transition from spiking to nonspiking, caused by a loss of voltage-gated Na currents. This change in membrane excitability occurred just after eye opening (P10), such that all of the starburst cells tested before eye opening had conspicuous tetrodotoxin-sensitive Na currents and action potentials, but none tested after the first 3 postnatal weeks had detectable Na currents or spikes. Our results suggest that starburst cells use action potentials transiently during development and probably play a functional role in visual development. These cells then cease to spike as the retina matures, presumably consistent with their role in visual processing in the mature retina.

Indexed as

Action PotentialsAgingAnimalsAnimals, NewbornIn Vitro TechniquesKineticsPatch-Clamp TechniquesRabbitsRetinaRetinal Ganglion CellsTetrodotoxinTime FactorsTetrodotoxin

Identifiers

PMID8755602
PMCPMC38874

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.