Developing Myopia in a Mouse Model Through Lens-Induced Defocusing

0 views • 2:48 min • April 28th, 2025

Loading...
$$\rightleftharpoonup{xx}$$ $$\longleftharp{xx}$$, $$\longrightharp{xx}$$,

Start with an anesthetized mouse with an exposed skull bone.

Apply an etching agent to remove the periosteum and create a cleaner surface.

Position the eyeglass holder with lens frames so the eyes are centered within the frames.

Apply adhesive to the holder and let it set, securing it to the skull.

Remove the lens frames to minimize discomfort during recovery.

Intraperitoneally inject a recovery agent to recover the mouse.

When the mouse is awake, reattach the frame containing concave lenses covering the eyes.

These lenses disperse incoming light, causing it to converge behind the retina and resulting in blurred vision.

Retinal neurons detect the blur and signal the brain to elongate the eyeball to focus the light on the retina for clear vision.

After the lenses are removed, the elongated eyeball causes light to converge in front of the retina, impairing near vision in the mouse and resulting in myopia.

To fix the previously prepared goggle frame onto the mouse, first, apply one drop of 0.1% purified sodium hyaluronate eye drop to each eye, and place the chin of the anesthetized mouse onto a sloped surface, so the up front plane of the cranium is horizontal. Use a cotton swab soaked with 70% ethanol to sterilize the hair and scalp between the ears and eyes, and make a 0.8 square centimeter incision in the skin between the ears and eyes to expose the skull. Use dental etching liquid in a cotton swab to remove the periosteum, and use a pair of frames without lenses to help fix the stick onto the right position, carefully adjusting the position of the frames to make sure that both eyes are in the middle of the empty frames.

Use a self-cured dental adhesive system to attach the stick onto the mouse head, and wait about five minutes before carefully removing the frame and the nut without changing the position of the stick. Then, inject 0.75 milligrams per kilogram of atipamezole hydrochloride intraperitoneally to help the mouse to recover from the anesthesia more quickly, and place the mouse into an individual cage until fully recovered. 24 hours after the surgery, grasp the stick and place the frames with lenses onto the animal to initiate the myopia induction.

05:56

Scleral Cross-linking Using Riboflavin and Ultraviolet-A Radiation for Prevention of Axial Myopia in a Rabbit Model

Related Videos

0 Views

05:32

A Detailed Protocol for Perspiration Monitoring Using a Novel, Small, Wireless Device

Related Videos

0 Views

12:25

Second Harmonic Generation Signals in Rabbit Sclera As a Tool for Evaluation of Therapeutic Tissue Cross-linking (TXL) for Myopia

Related Videos

0 Views

07:00

A Laser-induced Mouse Model of Chronic Ocular Hypertension to Characterize Visual Defects

Related Videos

0 Views

07:08

A Mouse Model for Laser-induced Choroidal Neovascularization

Related Videos

0 Views

09:26

A Magnetic Microbead Occlusion Model to Induce Ocular Hypertension-Dependent Glaucoma in Mice

Related Videos

0 Views

07:56

Sequential Application of Glass Coverslips to Assess the Compressive Stiffness of the Mouse Lens: Strain and Morphometric Analyses

Related Videos

0 Views

13:47

Laser Capture Microdissection of Highly Pure Trabecular Meshwork from Mouse Eyes for Gene Expression Analysis

Related Videos

0 Views

07:00

A Model of Glaucoma Induced by Circumlimbal Suture in Rats and Mice

Related Videos

0 Views

07:20

Inducement and Evaluation of a Murine Model of Experimental Myopia

Related Videos

0 Views

Last updated: 27 June 2026