We are thankful to Yingtian He for sharing data of direction tuning. This work was supported by grants from the Canadian Foundation of Innovation and Ontario Research Fund (CFI/ORF project no. 37597), NSERC (RGPIN-2019-06479), CIHR (Project Grant 437007), and Connaught New Researcher Awards.

All experimental procedures performed in this study were approved by the Biological Sciences Local Animal Care Committee, in accordance with guidelines established by the University of Toronto Animal Care Committee and the Canadian Council on Animal Care.
1. Implantation of a head bar on top of the skull
NOTE: To avoid the contribution of VOR behavior to the eye movements, the head of the mouse is immobilized during the OKR test. Therefore, a head bar...

Evaluating Optokinetic Reflex Responses in Mice: A New High-Precision Protocol

<ol>
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The method of the OKR behavioral assay presented here provides several advantages. First, computer-generated visual stimulation solves the intrinsic issues of physical drums. Dealing with the issue that physical drums do not support the systematic examination of spatial frequency, direction, or contrast tuning8, the virtual drum allows these visual parameters to be changed on a trial-by-trial basis, thus facilitating a systematic and quantitative analysis of the feature selectivity of the OKR beha...

In response to visual stimuli in the environment, our eyes move to shift our gaze, stabilize retinal images, track moving targets, or align the foveae of two eyes with targets located at different distances from the observer, which are vital to proper vision1,2. Oculomotor behaviors have been widely used as attractive models of sensorimotor integration to understand the neural circuits in health and disease, at least partly because of the simplicity of the oculomotor system3. Controlled by three pairs of extraocular muscles, the eye rotates in the socket primarily around three corresponding axes: elevation and depression along the transverse axis, adduction and abduction along the vertical axis, and intorsion and extorsion along the anteroposterior axis1,2. Such a simple system allows researchers to evaluate the oculomotor behaviors of mice easily and accurately in a lab environment.
One prime oculomotor behavior is the optokinetic reflex (OKR). This involuntary eye movement is triggered by slow drifts or slips of images on the retina and serves to stabilize retinal images as an animal&#39;s head or its surroundings move2,4. The OKR, as a behavioral paradigm, is interesting to researchers for several reasons. First, it can be stimulated reliably and quantified accurately5,6. Second, the procedures of quantifying this behavior are relatively simple and standardized and can be applied to evaluate the visual functions of a large cohort of animals7. Third, this innate behavior is highly plastic5,8,9. Its amplitude can be potentiated when repetitive retinal slips occur for a long time5,8,9, or when its working partner vestibular ocular reflex (VOR), another mechanism of stabilizing retinal images triggered by vestibular input2, is impaired5. These experimental paradigms of OKR potentiation empower researchers to unveil the circuit basis underlying oculomotor learning.
Two non-invasive methods have primarily been used to evaluate the OKR in previous studies: (1) video-oculography combined with a physical drum7,10,11,12,13 or (2) arbitrary determination of head turns combined with a virtual drum6,14,15,16. Although their applications have made fruitful discoveries in understanding the molecular and circuit mechanisms of oculomotor plasticity, these two methods each have some drawbacks which limit their powers in quantitatively examining the properties of the OKR. First, physical drums, with printed patterns of black and white stripes or dots, do not allow easy and quick changes of visual patterns, which largely restricts the measurement of the dependence of the OKR on certain visual features, such as spatial frequency, direction, and contrast of moving gratings8,17. Instead, tests of the selectivity of the OKR to these visual features can benefit from computerized visual stimulation, in which visual features can be conveniently modified from trial to trial. In this way, researchers can systematically examine the OKR behavior in the multi-dimensional visual parameter space. Moreover, the second method of the OKR assay reports only the thresholds of visual parameters that trigger discernible OKRs, but not the amplitudes of eye or head movements6, 14,15,16. The lack of quantitative power thus prevents analyzing the shape of tuning curves and the preferred visual features, or detecting subtle differences between individual mice in normal and pathological conditions. To overcome the above limitations, video-oculography and computerized virtual visual stimulation had been combined to assay the OKR behavior in recent studies5,17,18,19,20. However, these previously published studies did not provide enough technical details or step-by-step instructions, and consequently it is still challenging for researchers to establish such an OKR test for their own research.
Here, we present a protocol to precisely quantify the visual feature selectivity of OKR behavior under photopic or scotopic conditions with the combination of video-oculography and computerized virtual visual stimulation. Mice are head-fixed to avoid the eye movement evoked by vestibular stimulation. A high-speed camera is used to record the ocular movements from mice viewing moving gratings with changing visual parameters. The physical size of the eyeballs of individual mice is calibrated to ensure the accuracy of deriving the angle of eye movements21. This quantitative method allows comparing OKR behavior between animals of different ages or genetic backgrounds, or monitoring its change caused by pharmacological treatments or visual-motor learning.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>2D translational stage</td>
			<td>Thorlabs</td>
			<td>XYT1</td>
			<td></td>
		</tr>
		<tr>
			<td>Acrylic resin</td>
			<td>Lang Dental</td>
			<td>B1356</td>
			<td>For fixing headplate on skull and protecting skull</td>
		</tr>
		<tr>
			<td>Bupivacaine</td>
			<td>STERIMAX</td>
			<td>ST-BX223</td>
			<td>Bupivacaine Injection BP 0.5%. Local anesthesia</td>
		</tr>
		<tr>
			<td>Carprofen</td>
			<td>RIMADYL</td>
			<td>8507-14-1</td>
			<td>Analgesia</td>
		</tr>
		<tr>
			<td>Compressed air</td>
			<td>Dust-Off</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Eye ointment</td>
			<td>Alcon</td>
			<td>Systane</td>
			<td>For maintaining moisture of eyes</td>
		</tr>
		<tr>
			<td>Graphic card</td>
			<td>NVIDIA</td>
			<td>Geforce GTX 1650 or Quadro P620.</td>
			<td>For generating single screen among three monitors</td>
		</tr>
		<tr>
			<td>Heating pad</td>
			<td>Kent Scientific</td>
			<td>HTP-1500</td>
			<td>For maintaining body temperature</td>
		</tr>
		<tr>
			<td>High-speed infrared (IR) camera</td>
			<td>Teledyne Dalsa</td>
			<td>G3-GM12-M0640</td>
			<td>For recording eye rotation</td>
		</tr>
		<tr>
			<td>IR LED</td>
			<td>Digikey</td>
			<td>PDI-E803-ND</td>
			<td>For CR reference and the illumination of the eye</td>
		</tr>
		<tr>
			<td>IR mirror</td>
			<td>Edmund optics</td>
			<td>64-471</td>
			<td>For reflecting image of eye</td>
		</tr>
		<tr>
			<td>Isoflurane</td>
			<td>FRESENIUS KABI</td>
			<td>CP0406V2</td>
			<td></td>
		</tr>
		<tr>
			<td>Labview</td>
			<td>National instruments</td>
			<td>version 2014</td>
			<td>eye tracking</td>
		</tr>
		<tr>
			<td>Lactated ringer</td>
			<td>BAXTER</td>
			<td>JB2324</td>
			<td>Water and energy supply</td>
		</tr>
		<tr>
			<td>Lidocaine and epinephrine mix</td>
			<td>Dentsply Sirona</td>
			<td>82215-1</td>
			<td>XYLOCAINE. Local anesthesia</td>
		</tr>
		<tr>
			<td>Luminance Meter</td>
			<td>Konica Minolta</td>
			<td>LS-150</td>
			<td>for calibration of monitors</td>
		</tr>
		<tr>
			<td>Matlab</td>
			<td>MathWorks</td>
			<td>version xxx</td>
			<td>analysis of eye movements</td>
		</tr>
		<tr>
			<td>Meyhoefer Curette</td>
			<td>World Precision Instruments</td>
			<td>501773</td>
			<td>For scraping skull and removing fascia</td>
		</tr>
		<tr>
			<td>Microscope calibration slide</td>
			<td>Amscope</td>
			<td>MR095</td>
			<td>to measure the magnification of video-oculography</td>
		</tr>
		<tr>
			<td>Monitors</td>
			<td>Acer&#160;</td>
			<td>B247W</td>
			<td>Visual stimulation</td>
		</tr>
		<tr>
			<td>Neutral density filter</td>
			<td>Lee filters</td>
			<td>299</td>
			<td>to generate scotopic visual stimulation</td>
		</tr>
		<tr>
			<td>Nigh vision goggle</td>
			<td>Alpha optics</td>
			<td>AO-3277</td>
			<td>for scotopic OKR</td>
		</tr>
		<tr>
			<td>Photodiode</td>
			<td>Digikey</td>
			<td>TSL254-R-LF-ND</td>
			<td>to synchronize visual stimulation and video-oculography</td>
		</tr>
		<tr>
			<td>Pilocarpine hydrochloride</td>
			<td>Sigma-Aldrich</td>
			<td>P6503</td>
			<td></td>
		</tr>
		<tr>
			<td>Post</td>
			<td>Thorlabs</td>
			<td>TR1.5</td>
			<td></td>
		</tr>
		<tr>
			<td>Post holder</td>
			<td>Thorlabs</td>
			<td>PH1</td>
			<td></td>
		</tr>
		<tr>
			<td>PsychoPy</td>
			<td>open source software</td>
			<td>version xxx</td>
			<td>visual stimulation toolkit</td>
		</tr>
		<tr>
			<td>Scissor</td>
			<td>RWD</td>
			<td>S12003-09</td>
			<td>For skin removal</td>
		</tr>
		<tr>
			<td>Superglue</td>
			<td>Krazy Glue</td>
			<td></td>
			<td>Type: All purpose. For adhering headplate on the skull</td>
		</tr>
	</tbody>
</table>

quantification of visual feature selectivity of the optokinetic reflex in mice

The optokinetic reflex (OKR) is an essential innate eye movement that is triggered by the global motion of the visual environment and serves to stabilize retinal images. Due to its importance and robustness, the OKR has been used to study visual-motor learning and to evaluate the visual functions of mice with different genetic backgrounds, ages, and drug treatments. Here, we introduce a procedure for evaluating OKR responses of head-fixed mice with high accuracy. Head fixation can rule out the contribution of vestibular stimulation on eye movements, making it possible to measure eye movements triggered only by visual motion. The OKR is elicited by a virtual drum system, in which a vertical grating presented on three computer monitors drifts horizontally in an oscillatory manner or unidirectionally at a constant velocity. With this virtual reality system, we can systematically change visual parameters like spatial frequency, temporal/oscillation frequency, contrast, luminance, and the direction of gratings, and quantify tuning curves of visual feature selectivity. High-speed infrared video-oculography ensures accurate measurement of the trajectory of eye movements. The eyes of individual mice are calibrated to provide opportunities to compare the OKRs between animals of different ages, genders, and genetic backgrounds. The quantitative power of this technique allows it to detect changes in the OKR when this behavior plastically adapts due to aging, sensory experience, or motor learning; thus, it makes this technique a valuable addition to the repertoire of tools used to investigate the plasticity of ocular behaviors.

Author Spotlight: An Accurate and Quantitative Approach to Study Visual Feature Selectivity of the Optokinetic Reflex in Mice 

Quantification of Visual Feature Selectivity of the Optokinetic Reflex in Mice

We're interested in the capacity of retinal system in health and disease mouse model. Currently, we are using optokinetic reflex or OKR insured, which is our involuntary eye movement that serves to stabilize retinal images to understand how the retinal system contributes to the adaptive plasticity in retinal innate behaviors. OKR model studies have advanced our understanding of innate behavior plasticity by demonstrating that prolonged retinal stimulation or impaired by similar ocular reflex can increase the behavior amplitude.And by investigating the underlying molecular synaptic and secretory mechanisms. We combined video oculargraphy and computerized virtual visual stimulation to precisely quantify the OKR behavior invokes by truncating with freely changing parameters. This procedure is relatively simple and can be standardized to accommodate large scale studies.Our protocol accurately analyzes to include shapes and prefer visual features, detects subtle differences in normal and pathological conditions, and also can monitor changes in OKR due to pharmacological treatments or visual motor learning. The high precision and the quantitative power make it possible to compare repetitive OKR measurements of the same eyes in longitudinal studies and their different pharmacological treatments or under neurosurpreterations. It also provides opportunities to study the neurosurpres and the circuit mechanisms of OKR plasticity.

With the procedure detailed above, we evaluated the dependence of the OKR on several visual features. The example traces shown here were derived using the analysis codes provided in Supplementary Coding File 1, and the example traces raw file can be found in Supplementary Coding File 2. When the drum grating drifted in a sinusoidal trajectory (0.4 Hz), the animal&#39;s eye automatically followed the movement of the grating in a similar oscillatory manner (Figure 3B</...

Watch this Scientific Journal Video about An Accurate and Quantitative Approach to Study Visual Feature Selectivity of the Optokinetic Reflex in Mice at JoVE.com

Here, we describe a standard protocol for quantifying the optokinetic reflex. It combines virtual drum stimulation and video-oculography, and thus allows precise evaluation of the feature selectivity of the behavior and its adaptive plasticity.

The optokinetic reflex (OKR) is an essential innate eye movement that is triggered by the global motion of the visual environment and serves to stabilize ...

quantification-visual-feature-selectivity-optokinetic-reflex

Research

JoVE Journal

Neuroscience

1.2K ビュー.  University of Toronto Mississauga. 私たちは、健康と病気のマウスモデルにおける網膜系の容量に興味を持っています。現在、私たちは視運動性反射またはOKR保険を使用しており、これは網膜画像を安定させるのに役立つ不随意眼球運動であり、網膜系が網膜の生得的行動の適応可塑性にどのように寄与しているかを理解します。OKRモデル研究は、網膜への刺激が長引いたり、同様の眼反射によって障害?...

ビデオ: 著者スポットライト:マウスの視運動反射の視覚特徴選択性を研究するための正確で定量的なアプローチ 

Here, we describe a standard protocol for quantifying the optokinetic reflex. It combines virtual drum stimulation and video-oculography, and thus allows precise evaluation of the feature selectivity of the behavior and its adaptive plasticity.

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pyokr: a semi-automated method for quantifying optokinetic reflex tracking ability

Author Spotlight: A Streamlined and Accessible Analysis Method to Quantify Optokinetic Reflex Tracking Responses

We describe here PyOKR, a semi-automated quantitative analysis method that directly measures eye movements resulting from visual responses to two-dimensional image motion. A Python-based user interface and analysis algorithm allows for higher throughput and more accurate quantitative measurements of eye-tracking parameters than previous methods.

Python-Based Tool for Quantitative Optokinetic Reflex Assessment in Animals

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using the optokinetic response to study visual function of zebrafish

Using the optokinetic response to study visual function of zebrafish

Optokinetic response has been widely used to assess the visual functions of larval zebrafish. Nevertheless, the standard protocol for larval fish is not yet readily applicable in adults1-5. Here, we introduce how to measure the OKR of adult zebrafish using a new protocol which is established in our...

the optokinetic response as a quantitative measure of visual acuity in zebrafish

The Optokinetic Response as a Quantitative Measure of Visual Acuity in Zebrafish

Zebrafish have been a valuable tool for many research areas. Here we demonstrate a method to elicit a visual response and calculate a functional visual acuity in the adult...

PyOKR: A Semi-Automated Method for Quantifying Optokinetic Reflex Tracking Ability

recording eye movements of the optokinetic reflex (okr)

Recording Eye Movements of the Optokinetic Reflex (OKR)  

optokinetic response assay: a method to measure visual acuity in zebrafish

This video describes the optokinetic response assay in zebrafish. The video measures the reflexive eye movements based on the visual moving stimulus and determines the visual acuity in...

Optokinetic Response Assay: A Method to Measure Visual Acuity in Zebrafish

using optical coherence tomography and optokinetic response as structural and functional visual system readouts in mice and rats

Using Optical Coherence Tomography and Optokinetic Response As Structural and Functional Visual System Readouts in Mice and Rats

A detailed protocol for the assessment of structural and visual readouts in rodents by optical coherence tomography and optokinetic response is presented. The results provide valuable insights for ophthalmologic as well as neurologic...

investigating the deployment of visual attention before accurate and averaging saccades via eye tracking and assessment of visual sensitivity

Investigating the Deployment of Visual Attention Before Accurate and Averaging Saccades via Eye Tracking and Assessment of Visual Sensitivity

This experimental protocol combined eye tracking and the assessment of presaccadic visual sensitivity in a dual task paradigm, consisting of a free choice saccade task and a visual discrimination task, to investigate the deployment of visual spatial attention before both, accurate and averaging...

a visual approach for inducing dolichoectasia in mice to model large vessel-mediated cerebrovascular dysfunction

Author Spotlight: Modeling Vascular Contributions to Alzheimer&#039;s Disease in Transgenic Mice

We demonstrate chemically inducing large blood vessel dilatation in mice as a model for investigating cerebrovascular dysfunction, which can be used for vascular dementia and Alzheimer's disease modeling. We also demonstrate visualizing the vasculature by injecting silicone rubber compound and providing clear visual guidance for measuring changes in blood vessel...

A Visual Approach for Inducing Dolichoectasia in Mice to Model Large Vessel-Mediated Cerebrovascular Dysfunction

terminal h-reflex measurements in mice

Terminal H-reflex Measurements in Mice

The clinical evaluation of spasticity based on the Hoffmann reflex (H-reflex) and using electrical stimulation of peripheral nerves is an established method. Here, we provide a protocol for a terminal and direct nerve stimulation for H-reflex quantification in the mouse...

an automated method for assessing visual acuity in infants and toddlers using an eye-tracking system

Author Spotlight: An Automated Method for Assessing Visual Acuity in Infants and Toddlers Using an Eye-Tracking System  

In this paper, we present a novel automated method for assessing visual acuity in infants and toddlers by using an eye-tracking...

An Automated Assessment of Visual Acuity in Infants and Toddlers

python-based quantification of optokinetic reflex for animal eye movement analysis

Python-Based Quantification of Optokinetic Reflex for Animal Eye Movement Analysis

an in vitro approach to study mitochondrial dysfunction: a cybrid model

An In Vitro Approach to Study Mitochondrial Dysfunction: A Cybrid Model

Transmitochondrial cybrids are hybrid cells obtained by fusing mitochondrial DNA (mtDNA)-depleted cells (rho0 cells) with cytoplasts (enucleated cells) derived from patients affected by mitochondrial disorders. They allow the determination of the nuclear or mitochondrial origin of the disease, evaluation of biochemical activity, and confirmation of the pathogenetic role of mtDNA-related...

An In Vitro Approach to Study Mitochondrial Dysfunction: A Cybrid Model

intrathecal injection of newborn mouse for genome editing and drug delivery

Author Spotlight: Intrathecal Injection &amp;#8211; An Efficient and Reliable Delivery Method to Test the Efficacy of Gene Editing in Neonatal Mouse Brains

The present protocol outlines step-by-step instructions for performing intrathecal injections in neonatal mice for gene editing and drug...

A Comprehensive Protocol for Delivering Intrathecal Injections in Neonatal Mice

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cryo-section dissection of the adult subependymal zone for accurate and deep quantitative proteome analysis

Cryo-section Dissection of the Adult Subependymal Zone for Accurate and Deep Quantitative Proteome Analysis

Cryo-section-dissection allows fresh, frozen preparation of the largest neurogenic niche in the murine brain for deep quantitative proteome analysis. The method is precise, efficient, and causes minimal tissue perturbation. Therefore, it is ideally suited for studying the molecular microenvironment of this niche, as well as other organs, regions, and species.

a murine model of hyperlipidemia&#45;induced heart failure with preserved ejection fraction

Author Spotlight: Exploring the Relationship Between Lipotoxicity and HFpEF 

This protocol presents a detailed approach to replicating a murine model of hyperlipidemia-induced heart failure with preserved ejection fraction (HFpEF). The design combines the administration of adeno-associated virus 9-cardiac troponin T-low-density lipoprotein receptor (AAV9-cTnT-LDLR) and poloxamer-407...

Investigating HFpEF Pathophysiology in a Hyperlipidemia&amp;#45;Induced Mouse Model

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microhardness measurements on tooth and alveolar bone in rodent oral disease models

Author Spotlight: Establishing an Accurate Microhardness Testing Protocol for Craniofacial Tissues

Microhardness is a mechanical property and an informative parameter for evaluating hard tissue pathophysiology. Here, we demonstrate a standardized protocol (sample preparation, polishing, flat surface, and indentation sites) for microhardness analysis in tooth and alveolar bone in rodent oral disease models, namely, dental fluorosis, and ligature-induced periodontal bone...

Microhardness Protocol for Evaluating Rodent Oral Disease

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an improved method for accurate and rapid measurement of flight performance in drosophila

An Improved Method for Accurate and Rapid Measurement of Flight Performance in Drosophila

Here we describe a method for rapid and accurate measurement of flight performance in Drosophila, enabling high-throughput...

An Improved Method for Accurate and Rapid Measurement of Flight Performance in Drosophila

Implantation of a Head Bar on Top of the Mouse Skull

After anesthetizing the mouse, place it on a heating pad to maintain its body temperature. Apply a layer of lubricant eye ointment to both eyes and cover them with aluminum foil to protect them from light illumination. Then inject carprofen subcutaneously at a dose of 20 milligrams per kilogram to reduce the pain.Wet the fur on top of the skull with 4%chlorhexidine gluconate and shave the area. Disinfect the exposed scalp twice using 70%isopropyl alcohol and chlorhexidine alcohol. Next, inject bupivacaine subcutaneously at the incision site.Then remove the scalp with scissors to expose the dorsal surface of the skull, including the posterior frontal bone, parietal bone and interparietal bone. Apply several drops of 1%lidocaine and one to 100, 000 epinephrine on the exposed skull to reduce local pain and bleeding. Then scrape the skull with a Meyhoefer curette to remove the fascia, and clean it with PBS.Gently blow compressed air onto the skull surface until the moisture is gone and the bone turns whitish. Then apply a thin layer of super glue to the exposed surface of the skull, including the edge of the cut scalp. Followed by a layer of acrylic resin.Now place a stainless-steel head bar along the midline on top of the skull. And apply more acrylic resin, starting from the edge of the head bar, until its base is completely embedded in the acrylic resin. Wait for about 15 minutes until the acrylic resin hardens.Subcutaneously inject one milliliter of lactated Ringer's solution. Then return the mouse to a cage placed on a heating pad until the animal is fully mobile.

Calibration of Mouse Eye Movements

After setting up the virtual drum and video oculography, fix the animal's head on a customized stage. Adjust the tilt of the head so that the left and right eyes are leveled and the nasal and temporal corners of the eyes are aligned horizontally. Transfer the stage with the head-fixed animal to the center of the enclosure formed by the three monitors.Open the eye tracking software and click Free run. Then, click the Run button to turn on the camera. Adjust the position of the right eye until it appears at the center of the video.Rotate the camera arm to the left extreme end. Then, manually move the animal's right eye position on the horizontal plane perpendicular to the optical axis with fine adjustment of the 2D translational stage until the X-corneal reflection is at the horizontal center of the image. Now rotate the camera arm to the other end, and if the X-corneal reflection runs away from the center of the image, move the right eye along the optical axis with the fine adjustment until the X-corneal reflection comes to the center.Repeat several times until the X-corneal reflection stays in the center when the camera arm swings left and right. Click on the Calibration button and then the Run button. Turn on the Y-corneal reflection LED and record its position on the video.Then, switch to the X-corneal reflection LED and record its position. To measure the radius of pupil rotation, rotate the camera arm to the left end. Record the positions of the pupil and X-corneal reflection on the video by right-clicking the mouse, then rotate the camera arm to the right end.Record the positions of the pupil and X-corneal reflection on the video. Based on the recorded values, calculate the radius of pupil rotation, Rp, using this formula. To develop the relationship between pupil rotation and pupil diameter, adjust the luminance of the monitors from 0 to 160 candela per square meter to control the pupil size, and record the pupil diameter for each luminance value.For each luminance value, measure the radius of pupil rotation 8 to 10 times and record the diameter of the pupil. Then, use linear regression to analyze the relationship between the radius of pupil rotation, Rp, and pupil diameter, and to derive the slope and intercept of the linear model.

After fixing the head of the mouse in the rig and calibrating the eye movements, lock the camera arm at the central position. Run the visual stimulation and eye tracking software. For photopic OKR measurement, ensure the drum grating oscillates horizontally with a sinusoidal trajectory.For scotopic OKR, to achieve scotopic visual stimulation, cover the screen of each monitor with a customized filter made of five layers of 1.2 neutral density film, and turn the room light off. Apply one drop of pilocarpine solution to the right eye, and wait 15 minutes to shrink the pupil to a proper size for eye tracking under the scotopic condition. Ensure the drop stays on the eye and is not wiped away by the mouse.Afterward, rinse the right eye with saline to thoroughly wash away the pilocarpine solution. Finally, pull down the curtain to completely seal the enclosure, which prevents stray light from interfering with the scotopic vision. Run the visual stimulation and the eye tracking software.For scotopic OKR measurement, ensure the drum grating drifts at a constant velocity from left to right, the temporonasal direction about the left eye. The OKR gain varied with the values of spatial frequency, oscillation frequency, and the direction of movement grating. The spatial frequency tuning curve of the OKR behavior peaked at an intermediate spatial frequency of 0.16 cycles per degree.The oscillation frequency tuning curve monotonically declined as the oscillation frequency of the drum grating increased. The horizontal OKR could also be induced by gratings moving in different directions, but the strongest horizontal OKR behavior was elicited by the temporonasal motion. Following 45 minutes of continuous OKR stimulation, the amplitude of the OKR behavior was significantly potentiated.