Evidence map›Paper›PMID 30633847›Full record

ArticleThe European journal of neuroscience2019

Synchronized activation of striatal direct and indirect pathways underlies the behavior in unilateral dopamine-depleted mice.

Omar Jáidar, Luis Carrillo-Reid, Yoko Nakano, Violeta Gisselle Lopez-Huerta, Arturo Hernandez-Cruz, José Bargas, Marianela Garcia-Munoz, Gordon William Arbuthnott

Open access · hybridAbstract read
In one paragraph

Article in The European journal of neuroscience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 29 citations in OpenAlex.

  1. Timing and Convergence of Ensemble Activity Govern Auditory Thalamocortical Transmission.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  2. Article
  3. Pathological cell assembly dynamics in a striatal MSN network model.Frontiers in computational neuroscience · 2024
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Ramping activity in the striatum.Frontiers in computational neuroscience · 2022
    Article
  10. Article
  11. Article
  12. Experience-related enhancements in striatal temporal encoding.The European journal of neuroscience · 2021
    Article
  13. Article
  14. Synaptic Pruning by Microglia in Epilepsy.Journal of clinical medicine · 2019
    Review
  15. Article
  16. Dopamine DASN neuro
    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

8 authors at 1 institution in 1 country.

Omar JáidarOkinawa Institute of Science and Technology Graduate University, Okinawa, Japan.
Luis Carrillo-ReidOkinawa Institute of Science and Technology Graduate University, Okinawa, Japan.
Yoko NakanoOkinawa Institute of Science and Technology Graduate University, Okinawa, Japan.
Violeta Gisselle Lopez-HuertaOkinawa Institute of Science and Technology Graduate University, Okinawa, Japan.
Arturo Hernandez-CruzOkinawa Institute of Science and Technology Graduate University, Okinawa, Japan.
José BargasOkinawa Institute of Science and Technology Graduate University, Okinawa, Japan.ORCID 0000-0002-8205-8163
Marianela Garcia-MunozOkinawa Institute of Science and Technology Graduate University, Okinawa, Japan.
Gordon William ArbuthnottOkinawa Institute of Science and Technology Graduate University, Okinawa, Japan.ORCID 0000-0002-3386-8362
Okinawa Institute of Science and Technology Graduate University · JP

Funding

Government of Japan
6 · The paper itself

Abstract

For more than three decades it has been known, that striatal neurons become hyperactive after the loss of dopamine input, but the involvement of dopamine (DA) D1- or D2-receptor-expressing neurons has only been demonstrated indirectly. By recording neuronal activity using fluorescent calcium indicators in D1 or D2 eGFP-expressing mice, we showed that following dopamine depletion, both types of striatal output neurons are involved in the large increase in neuronal activity generating a characteristic cell assembly of particular neurons that dominate the pattern. When we expressed channelrhodopsin in all the output neurons, light activation in freely moving animals, caused turning like that following dopamine loss. However, if the light stimulation was patterned in pulses the animals circled in the other direction. To explore the neuronal participation during this stimulation we infected normal mice with channelrhodopsin and calcium indicator in striatal output neurons. In slices made from these animals, continuous light stimulation for 15 s induced many cells to be active together and a particular dominant group of neurons, whereas light in patterned pulses activated fewer cells in more variable groups. These results suggest that the simultaneous activity of a large dominant group of striatal output neurons is intimately associated with parkinsonian symptoms.

Indexed as

AnimalsBasal GangliaCalciumCorpus StriatumDopamineMaleMiceNeuronsParkinson Disease, SecondaryReceptors, Dopamine D1Receptors, Dopamine D2CalciumDopamineReceptors, Dopamine D1Receptors, Dopamine D2assembliesbasal gangliacalcium imagingoptogeneticsParkinson's disease

Identifiers

PMID30633847
PMCPMC6767564
OpenAlexW2911106714

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.