Evidence map›Paper›PMID 36194625›Full record

ArticlePLoS computational biology2022

Dual STDP processes at Purkinje cells contribute to distinct improvements in accuracy and speed of saccadic eye movements.

Lorenzo Fruzzetti, Hari Teja Kalidindi, Alberto Antonietti, Cristiano Alessandro, Alice Geminiani, Claudia Casellato, Egidio Falotico, Egidio D'Angelo

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

4 citing papers in PubMed, 11 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

8 authors at 4 institutions in 2 countries.

Lorenzo FruzzettiThe BioRobotics Institute, Scuola Superiore Sant'Anna, Pontedera (Pisa), Italy.ORCID 0000-0001-8294-6606
Hari Teja KalidindiInstitute of Information and Communication Technologies, Electronics and Applied Mathematics, Universite Catholique de Louvain, Ottignies-Louvain-la-Neuve, Belgium.ORCID 0000-0003-2634-7953
Alberto AntoniettiDepartment of Electronics, Information and Bioengineering, Politecnico di Milano, Milano, Italy.ORCID 0000-0003-0388-6321
Cristiano AlessandroDepartment of Brain and Behavioral Sciences, University of Pavia, Italy.ORCID 0000-0003-0655-4189
Alice GeminianiDepartment of Brain and Behavioral Sciences, University of Pavia, Italy.ORCID 0000-0002-9407-8719
Claudia CasellatoDepartment of Brain and Behavioral Sciences, University of Pavia, Italy.ORCID 0000-0002-8729-0391
Egidio FaloticoThe BioRobotics Institute, Scuola Superiore Sant'Anna, Pontedera (Pisa), Italy.
Egidio D'AngeloDepartment of Brain and Behavioral Sciences, University of Pavia, Italy.ORCID 0000-0002-6007-7187
University of Pavia · ITScuola Superiore Sant'Anna · ITPolitecnico di Milano · ITUCLouvain · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Saccadic eye-movements play a crucial role in visuo-motor control by allowing rapid foveation onto new targets. However, the neural processes governing saccades adaptation are not fully understood. Saccades, due to the short-time of execution (20-100 ms) and the absence of sensory information for online feedback control, must be controlled in a ballistic manner. Incomplete measurements of the movement trajectory, such as the visual endpoint error, are supposedly used to form internal predictions about the movement kinematics resulting in predictive control. In order to characterize the synaptic and neural circuit mechanisms underlying predictive saccadic control, we have reconstructed the saccadic system in a digital controller embedding a spiking neural network of the cerebellum with spike timing-dependent plasticity (STDP) rules driving parallel fiber-Purkinje cell long-term potentiation and depression (LTP and LTD). This model implements a control policy based on a dual plasticity mechanism, resulting in the identification of the roles of LTP and LTD in regulating the overall quality of saccade kinematics: it turns out that LTD increases the accuracy by decreasing visual error and LTP increases the peak speed. The control policy also required cerebellar PCs to be divided into two subpopulations, characterized by burst or pause responses. To our knowledge, this is the first model that explains in mechanistic terms the visual error and peak speed regulation of ballistic eye movements in forward mode exploiting spike-timing to regulate firing in different populations of the neuronal network. This elementary model of saccades could be extended and applied to other more complex cases in which single jerks are concatenated to compose articulated and coordinated movements.

Indexed as

Purkinje CellsSaccadesCerebellumEye MovementsNeuronal Plasticity

Identifiers

PMID36194625
PMCPMC9565489
OpenAlexW4301181055

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.