Affiliations: Department of Neuroscience, State Univesity of New
York at Stony Brook, Stony Brook, NY, USA | Center for Imaging and Neuroscience, Department of
Medicine, Brookhaven National Laboratory, Upton, NY, USA | Department of Orthopedic Surgery, Kyoto Prefectural
University of Medicine, Kyoto, Japan | Microsurgical Research Center, Department of Surgery,
Eastern Virginia Medical School, Norfolk, VA 23507, USA
Note: [] Corresponding author: J.K. Terzis, Microsurgical Research Center, Department of Surgery,
Eastern Virginia Medical School, Norfolk, VA 23507, USA. Tel.: +1 757 446 5272; Fax: +1 757 446 5109
Abstract: Among the pathological sequelae of facial paralysis is a paralytic eye. Apart from the psychological and aesthetic deficits, facial paralysis if left untreated can lead to dryness, ulceration and eventual blindness. Although numerous restorative microsurgical approaches have been introduced to address the sequelae of this problem, complete restoration of function to denervated facial muscles remains elusive.
Utilizing the rat model of facial paralysis the present research has as an objective to examine a dual treatment approach. Specifically, this study combined the current microsurgical treatment of the cross-facial nerve graft with local administration of insulin-like growth factor I (IGF-I).
The efficacy of this combined approach (cross-facial nerve graft + IGF-I) was assessed in the following ways: (a) behavior measurement of the blink response and (b) histomorphometry light and electron microscopy of the entire nerve graft. These data will help provide insight into the restoration of facial muscle function after trauma and assist in the future development of more potent treatment strategies.
7he local adnünistration of IGF-I (50 µg/ml) to the cross-facial nerve graft was found to restore the blink response faster and to strengthen the degree of eye closure. Light microscopy examination revealed that IGF-I significantly enhanced axonal regeneration within a nerve graft (a 22% increase in the mean number of axons), and increased the mean nerve fiber diameter and myelin thickness. Electron microscopy assessment of the nerve grafts demonstrated that the IGF-I treated grafts possessed a greater density of microtubules, which were evenly distributed within the axoplasm.
