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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Amniotic membrane as a biological dressing for 5-fluoruracil-induced oral mucositis in rats

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Author(s):
Lima, G. de M. G. [1] ; Severo, M. C. [1] ; Santana-Melo, G. de F. [1] ; Carvalho, M. A. [1] ; Vilela-Goulart, M. das G. [1] ; Salgado, M. A. C. [1] ; Gomes, M. F. [1]
Total Authors: 7
Affiliation:
[1] Univ Estadual Paulista, Dept Biosci & Oral Diag, BR-12245000 Sao Paulo - Brazil
Total Affiliations: 1
Document type: Journal article
Source: International Journal of Oral and Maxillofacial Surgery; v. 44, n. 7, p. 845-851, JUL 2015.
Web of Science Citations: 1
Abstract

Oral mucositis is a reaction to chemoradiation therapy during cancer treatment. The aim of this study was to investigate the use of amniotic membrane as a biological dressing for oral mucositis lesions in rats. Sixty Wistar rats were divided into three groups (n=20): control, 5-fluoruracil (5-FU), 5-fiuoruracil + amniotic membrane (5-FU + AM). Each group was subdivided (n=5) according to the time interval to sacrifice (3, 7, 14, and 21 days). Histology (haematoxylin eosin staining) and immunocytochemistry (anti-rat antibodies CD4, CD8, VEGF, and PCNA) were evaluated. Immunocytochemistry results were analyzed using one-way ANOVA and Tukey tests. The amniotic membrane (5FU + AM) played an important role in cell proliferation (PCNA 3 days 27.08 +/- 4.65, 7 days 27.90 +/- 3.34) and especially in neovascularization (VEGF 3 days 23.00 +/- 1.40, 7 days 26.00 +/- 0.95) for all time intervals, when compared to 5-FU (PCNA 3 days 23.12 +/- 1.61, 7 days 37.21 +/- 1.20; VEGF 3 days 17.05 +/- 1.51, 7 days 8.45 +/- 1.35) and control (PCNA 3 days 29.99 +/- 0.92, 7 days 16.33 +/- 2.88; VEGF 3 days 13.65 +/- 0.55, 7 days 15.70 +/- 1.39). It was biocompatible, showing significant differences compared to the other groups in CD4 (F=40.72; P=0.001) and CD8 (F=69.99, P=0.001) staining together, only during the inflammation phase (7 days) Amniotic membrane presented biocompatibility and stimulated cell proliferation and neovascularization, functioning as a promising biological dressing. (AU)