Changes in facial nerve function, morphology and neurotrophic factor III expression following three types of facial nerve injury.
- Author:
Lili ZHANG
1
;
Haibo WANG
;
Zhaomin FAN
;
Yuechen HAN
;
Lei XU
;
Haiyan ZHANG
Author Information
1. Department of Otolaryngology-Head and Neck Surgery, Shandong Provincial Hospital, Jinan, 250021, China. whbotologic797@163.com
- Publication Type:Journal Article
- MeSH:
Animals;
Facial Nerve;
metabolism;
pathology;
physiopathology;
Facial Nerve Injuries;
classification;
metabolism;
pathology;
physiopathology;
Neurotrophin 3;
metabolism;
Rats;
Rats, Wistar
- From:
Journal of Clinical Otorhinolaryngology Head and Neck Surgery
2011;25(2):78-81
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To study the changes in facial nerve function, morphology and neurotrophic factor III (NT-3) expression following three types of facial nerve injury.
METHOD:Changes in facial nerve function (in terms of blink reflex (BF), vibrissae movement (VM) and position of nasal tip) were assessed in 45 rats in response to three types of facial nerve injury: partial section of the extratemporal segment (group one), partial section of the facial canal segment (group two) and complete transection of the facial canal segment lesion (group three). All facial nerves specimen were then cut into two parts at the site of the lesion after being taken from the lesion site on 1st, 7th, 21st post-surgery-days (PSD). Changes of morphology and NT-3 expression were evaluated using the improved trichrome stain and immunohistochemistry techniques ,respectively.
RESULT:Changes in facial nerve function: In group 1, all animals had no blink reflex (BF) and weak vibrissae movement (VM) at the 1st PSD; The blink reflex in 80% of the rats recovered partly and the vibrissae movement in 40% of the rats returned to normal at the 7th PSD; The facial nerve function in 600 of the rats was almost normal at the 21st PSD. In group 2, all left facial nerve paralyzed at the 1st PSD; The blink reflex partly recovered in 40% of the rats and the vibrissae movement was weak in 80% of the rats at the 7th PSD; 8000 of the rats'BF were almost normal and 40% of the rats' VM completely recovered at the 21st PSD. In group 3, The recovery couldn't happen at anytime. Changes in morphology: In group 1, the size of nerve fiber differed in facial canal segment and some of myelin sheath and axons degenerated at the 7th PSD; The fibres' degeneration turned into regeneration at the 21st PSD; In group 2, the morphologic changes in this group were familiar with the group 1 while the degenerated fibers were more and dispersed in transection at the 7th PSD; Regeneration of nerve fibers happened at the 21st PSD. In group 3, most of the fibers crumbled at the 7th PSD and no regeneration was seen at the 21st PSD. Changes in NT-3: Positive staining of NT-3 was largely observed in axons at the 7th PSD, although little NT-3 was seen in the normal fibers.
CONCLUSION:Facial palsy of the rats in group 2 was more extensive than that in group 1 and their function partly recovers at the 21st PSD. The fibres' degeneration occurs not only dispersed throughout the injury site but also occurred throught the length of the nerve. NT-3 immunoreactivity increased in activated fibers after partial transection.
