Evidence map›Paper›PMID 38242692›Full record

ArticleeNeuro2024

Disynaptic Inhibitory Cerebellar Control Over Caudal Medial Accessory Olive.

Willem S van Hoogstraten, Marit C C Lute, Zhiqiang Liu, Robin Broersen, Luca Mangili, Lieke Kros, Zhenyu Gao, Xiaolu Wang, Arn M J M van den Maagdenberg, Chris I De Zeeuw

Open access · goldAbstract read
In one paragraph

Article in eNeuro, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

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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

10 authors at 3 institutions in 1 country.

Willem S van HoogstratenDepartment of Neuroscience, Erasmus MC, Rotterdam 3015 GD, The Netherlands w.vanhoogstraten@erasmusmc.nl c.dezeeuw@erasmusmc.nl.ORCID https://orcid.org/0000-0002-3635-4893
Marit C C LuteDepartment of Neuroscience, Erasmus MC, Rotterdam 3015 GD, The Netherlands.
Zhiqiang LiuDepartment of Neuroscience, Erasmus MC, Rotterdam 3015 GD, The Netherlands.
Robin BroersenDepartment of Neuroscience, Erasmus MC, Rotterdam 3015 GD, The Netherlands.
Luca MangiliDepartment of Neuroscience, Erasmus MC, Rotterdam 3015 GD, The Netherlands.
Lieke KrosDepartment of Neuroscience, Erasmus MC, Rotterdam 3015 GD, The Netherlands.
Zhenyu GaoDepartment of Neuroscience, Erasmus MC, Rotterdam 3015 GD, The Netherlands.ORCID https://orcid.org/0000-0002-4979-2366
Xiaolu WangDepartment of Neuroscience, Erasmus MC, Rotterdam 3015 GD, The Netherlands.
Arn M J M van den MaagdenbergDepartments of Neurology, Leiden University Medical Center, Leiden 2333 ZA, The Netherlands.ORCID https://orcid.org/0000-0002-9310-5535
Chris I De ZeeuwDepartment of Neuroscience, Erasmus MC, Rotterdam 3015 GD, The Netherlands w.vanhoogstraten@erasmusmc.nl c.dezeeuw@erasmusmc.nl.ORCID https://orcid.org/0000-0001-5628-8187
Erasmus University Rotterdam · NLNetherlands Institute for Neuroscience · NLLeiden University Medical Center · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The olivocerebellar system, which is critical for sensorimotor performance and learning, functions through modules with feedback loops. The main feedback to the inferior olive comes from the cerebellar nuclei (CN), which are predominantly GABAergic and contralateral. However, for the subnucleus d of the caudomedial accessory olive (cdMAO), a crucial region for oculomotor and upper body movements, the source of GABAergic input has yet to be identified. Here, we demonstrate the existence of a disynaptic inhibitory projection from the medial CN (MCN) to the cdMAO via the superior colliculus (SC) by exploiting retrograde, anterograde, and transsynaptic viral tracing at the light microscopic level as well as anterograde classical and viral tracing combined with immunocytochemistry at the electron microscopic level. Retrograde tracing in Gad2-Cre mice reveals that the cdMAO receives GABAergic input from the contralateral SC. Anterograde transsynaptic tracing uncovered that the SC neurons receiving input from the contralateral MCN provide predominantly inhibitory projections to contralateral cdMAO, ipsilateral to the MCN. Following ultrastructural analysis of the monosynaptic projection about half of the SC terminals within the contralateral cdMAO are GABAergic. The disynaptic GABAergic projection from the MCN to the ipsilateral cdMAO mirrors that of the monosynaptic excitatory projection from the MCN to the contralateral cdMAO. Thus, while completing the map of inhibitory inputs to the olivary subnuclei, we established that the MCN inhibits the cdMAO via the contralateral SC, highlighting a potential push-pull mechanism in directional gaze control that appears unique in terms of laterality and polarity among olivocerebellar modules.

Indexed as

CerebellumInferior Olivary ComplexAnimalsCerebellar NucleiMiceOlivary NucleusSynaptic Transmissioncerebellumgaze controlinferior oliveMedial accessory oliveolivocerebellar systemsuperior colliculus

Identifiers

PMID38242692
PMCPMC10875979
OpenAlexW4391020050

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.