# A neuronal process of the error signal that drives saccade adaptation

> **NIH NIH R01** · UNIVERSITY OF WASHINGTON · 2020 · $457,750

## Abstract

Project Summary/Abstract
 An impaired movement due to stroke, injury or aging recovers gradually. Can we speed up the
recovery process to achieve the rehabilitation faster? To repair an inaccurate movement, the brain measures
the error of the movement, namely the mismatch between the desired movement and the actual dysmetric
movement, and changes the movement to minimize the error. This process is called motor adaptation. The
speed of adaptation depends on its sensitivity to the error, i.e., the higher the error sensitivity, the faster the
adaptation. Theoretical models and neurophysiological studies suggest that the complex spikes of Purkinje
cells in the cerebellum encode the error. However, the neurons that deal with the error sensitivity are unknown.
Knowing the neuronal mechanisms that control error sensitivity has important implications for setting strategies
for the most efficient recovery strategy.
 In our last grant, we used saccade adaptation as a model system of motor adaptation. When we
arranged that each saccade missed its target by a constant error, the adaptation speed decreased gradually
during the adaptation session. This indicates that the sensitivity to the constant error decreased during the
session. We found that the visual sensitivity of superior colliculus (SC) neurons decreased as the error
sensitivity decreased. The visual activity of the SC has been suggested as a source of the complex spikes in
the cerebellum, which encode the error of the movement. Therefore, the SC visual activity could provide an
error sensitivity signal to the cerebellum.
 In this next grant period, we propose to examine how the visual activity of SC neurons is shaped to
encode the error sensitivity. Many brain structures project to the SC, but one of the best candidates to shape
SC activity is the Substantia Nigra pars reticulata (SNr) of the basal ganglia because it inhibits the SC directly.
Moreover, because patients with Parkinson’s disease, which affects the basal ganglia, show a slower saccade
adaptation, it seems likely that the basal ganglia affect the signal that controls the adaptation speed.
 To test this hypothesis, we will study the SNr with three complementary approaches. First, we will
record SNr activity during saccade adaptation and determine whether any component of SNr discharge is
related to error sensitivity. Second, we will determine the effect of SNr inactivation on saccade adaptation. We
expect that inactivation will affect the adaptation speed. Third, we will determine the effect that SNr
inactivation has on the activity of SC neurons. We expect that SNr inactivation will influence the visual activity
of neurons in the rostral SC, which is related to the error sensitivity.
 We predict that the results of these three projects will reveal a previously unsuspected role for the basal
ganglia in controlling the adaptation speed for cerebellar-dependent motor adaptation.

## Key facts

- **NIH application ID:** 9994313
- **Project number:** 5R01EY023277-08
- **Recipient organization:** UNIVERSITY OF WASHINGTON
- **Principal Investigator:** Yoshiko Kojima
- **Activity code:** R01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2020
- **Award amount:** $457,750
- **Award type:** 5
- **Project period:** 2013-08-01 → 2022-07-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/9994313

## Citation

> US National Institutes of Health, RePORTER application 9994313, A neuronal process of the error signal that drives saccade adaptation (5R01EY023277-08). Retrieved via AI Analytics 2026-05-23 from https://api.ai-analytics.org/grant/nih/9994313. Licensed CC0.

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