Evidence map›Paper›PMID 30988338›Full record

ArticleScientific reports2019

Reevaluating the ability of cerebellum in associative motor learning.

Da-Bing Li, Juan Yao, Lin Sun, Bing Wu, Xuan Li, Shu-Lei Liu, Jing-Ming Hou, Hong-Liang Liu, Jian-Feng Sui, Guang-Yan Wu

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 32% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Cerebellar Prediction and Feeding Behaviour.Cerebellum (London, England) · 2023
    Review
  5. Article
  6. Article
  7. Article
  8. The Optogenetic Revolution in Cerebellar Investigations.International journal of molecular sciences · 2020
    Review
  9. 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

10 authors at 3 institutions in 1 country.

Da-Bing LiExperimental Center of Basic Medicine, College of Basic Medical Sciences, Army Medical University, Chongqing, 400038, China.
Juan YaoExperimental Center of Basic Medicine, College of Basic Medical Sciences, Army Medical University, Chongqing, 400038, China.
Lin SunExperimental Center of Basic Medicine, College of Basic Medical Sciences, Army Medical University, Chongqing, 400038, China.
Bing WuExperimental Center of Basic Medicine, College of Basic Medical Sciences, Army Medical University, Chongqing, 400038, China.
Xuan LiExperimental Center of Basic Medicine, College of Basic Medical Sciences, Army Medical University, Chongqing, 400038, China.
Shu-Lei LiuExperimental Center of Basic Medicine, College of Basic Medical Sciences, Army Medical University, Chongqing, 400038, China.
Jing-Ming HouDepartment of Rehabilitation, Southwest Hospital, Army Medical University, Chongqing, 646000, China.
Hong-Liang LiuDepartment of Rehabilitation, Southwest Hospital, Army Medical University, Chongqing, 646000, China.
Jian-Feng SuiExperimental Center of Basic Medicine, College of Basic Medical Sciences, Army Medical University, Chongqing, 400038, China. jfsui2003@163.com.
Guang-Yan WuExperimental Center of Basic Medicine, College of Basic Medical Sciences, Army Medical University, Chongqing, 400038, China. wgy009@163.com.
Army Medical University · CNSouthwest Hospital · CNSouthwest Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It has been well established that the cerebellum and its associated circuitry constitute the essential neuronal system for both delay and trace classical eyeblink conditioning (DEC and TEC). However, whether the cerebellum is sufficient to independently modulate the DEC, and TEC with a shorter trace interval remained controversial. Here, we used direct optogenetic stimulation of mossy fibers in the middle cerebellar peduncle (MCP) as a conditioned stimulus (CS) replacement for the peripheral CS (eg, a tone CS or a light CS) paired with a periorbital shock unconditioned stimulus (US) to examine the ability of the cerebellum to learn the DEC and the TEC with various trace intervals. Moreover, neural inputs to the pontine nucleus (PN) were pharmacological blocked to limit the associative motor learning inside the cerebellum. We show that all rats quickly acquired the DEC, indicating that direct optogenetic stimulation of mossy fibers in the left MCP is a very effective and sufficient CS to establish DEC and to limit the motor learning process inside the cerebellum. However, only five out of seven rats acquired the TEC with a 150-ms trace interval, three out of nine rats acquired the TEC with a 350-ms trace interval, and none of the rats acquired the TEC with a 500-ms trace interval. Moreover, pharmacological blocking glutamatergic and GABAergic inputs to the PN from the extra-cerebellar and cerebellar regions has no significant effect on the DEC and TEC learning with the optogenetic CS. These results indicate that the cerebellum has the ability to independently support both the simple DEC, and the TEC with a trace interval of 150 or 350 ms, but not the TEC with a trace interval of 500 ms. The present results are of great importance in our understanding of the mechanisms and ability of the cerebellum in associative motor learning and memory.

Indexed as

Association LearningAnimalsBlinkingCerebellumConditioning, ClassicalConditioning, EyelidMaleMemoryNeural PathwaysOptogeneticsRatsRats, Sprague-Dawley

Identifiers

PMID30988338
PMCPMC6465343
OpenAlexW2937210963

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.