Basic fibroblast growth factor and epidermal growth factor reverse impaired ulcer healing of the rabbit oral mucosa

被引:93
作者
Fujisawa, K [1 ]
Miyamoto, Y [1 ]
Nagayama, M [1 ]
机构
[1] Univ Tokushima, Sch Dent, Dept Oral & Maxillofacial Surg 1, Tokushima 7708504, Japan
关键词
bFGF; EGF; impaired ulcer healing; oral mucosa; wound healing; FACTOR-BETA; DESALIVATED RATS; TISSUE-REPAIR; WOUNDS; MODEL; EXPRESSION; SALIVA; MICE;
D O I
10.1034/j.1600-0714.2003.t01-1-00111.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background: The therapies for refractory ulcers on the oral mucosa are symptomatic and very unsatisfactory. We hypothesized that application of growth factors might be able to achieve successful remission of the lesion. We evaluated the effects of systemic administration and topical application of epidermal growth factor (EGF) and basic fibroblast growth factor (bFGF) on impaired wound healing of ulcers in the rabbit gingiva. Methods: Almost uniform round ulcers could be created on the gingiva of the rabbits by chemical injury with acetic acid. When the submandibular glands were removed or i.v. injection of cisplatin (CDDP) and peplomycin sulfate was performed before ulcer formation, healing of the ulcers took longer than in untreated rabbits. To ascertain whether or not human EGF and bFGF affect rabbit cells, we first examined the effects of EGF and bFGF on the proliferation of the cells derived from rabbit gingiva. We then applied EGF or bFGF in these impaired healing models. Results: EGF and bFGF promoted proliferation of the fibroblasts, and EGF also promoted proliferation of the keratinocytes isolated from gingival tissue of rabbits in vitro . Systemic injections of EGF and bFGF in rabbits, which had their submandibular glands removed, and topical application of bFGF accelerated healing of ulcers created in rabbits injected with CDDP and peplomycin sulfate. The ability of bFGF to promote the healing of ulcers was much greater than that of EGF. Conclusion: Basic FGF may be effective for refractory oral mucosal lesions.
引用
收藏
页码:358 / 366
页数:9
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