Mice were anesthetized with isoflurane inhalation. Surgery was performed under an Omano surgical microscope (OM2300S-V7, 7-40X). A 1–1.5 cm midline neck incision was used. The superficial tissues were bluntly dissected and lateralized with a mini retractor. The neck muscles were gently dissected to locate the mouse’s right auditory bulla and the auditory capsule on the right side of the head, which are the landmarks to locate the foramen lacerum. A prepared piece of Surgifoam (Ethicon) at approximately 1–1.5 mg was gently delivered into the foramen lacerum using curved forceps. The Surgifoam was positioned between the trigeminal nerve root and the cochlea bulla. After removing the retractor and replacing the tissues, the skin was closed with 6-0 nylon monofilament (Ethicon) sutures. Mice in the sham group underwent the same surgical procedure including neck shaving, skin incision, muscle dissection, and foramen lacerum exposure without nerve root compression. The duration of the surgery ranged from 8 to 12 minutes per mouse. Tamoxifen was intraperitoneally administrated to Fos-iCre-ERT2 (Fos2A-iCreER-knockin) mice immediately after the FLIT procedure.
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