Glycosaminoglycan biosynthesis during 5-fluoro-2-deoxyuridine-induced palatal clefts in the rat

• Published in: Archives of oral biology 1997-05, Vol.42 (5), p.355-363
• Main Authors: Singh, G.D., Moxham, B.J., Langley, M.S., Embery, G.
• Format: Article
• Language: English
• Subjects: Animals; Chondroitin Sulfates - analysis; Chondroitin Sulfates - biosynthesis; cleft palate; Cleft Palate - chemically induced; Cleft Palate - embryology; Cleft Palate - metabolism; Densitometry; Dermatan Sulfate - analysis; Dermatan Sulfate - biosynthesis; Electrophoresis, Cellulose Acetate; Extracellular Matrix - chemistry; Extracellular Matrix - drug effects; Fetus; Floxuridine - adverse effects; glycosaminoglycans; Glycosaminoglycans - analysis; Glycosaminoglycans - biosynthesis; Heparitin Sulfate - analysis; Heparitin Sulfate - biosynthesis; Hyaluronic Acid - analysis; Hyaluronic Acid - biosynthesis; Mesoderm - drug effects; Mesoderm - metabolism; Palate - chemistry; Palate - drug effects; Palate - embryology; Palate, Soft - chemistry; Palate, Soft - drug effects; Palate, Soft - embryology; palatogenesis; rat; Rats; Rats, Wistar
• ISSN: 0003-9969; 1879-1506
• DOI: 10.1016/S0003-9969(97)00031-9

The biosynthesis and hydration of glycosaminoglycans (GAG) has been implicated in the generation of palatal shelf-elevating force(s) in mammals, although the nature of the palatal shelf extracellular matrices during cleft palate formation remains poorly understood. This study quantifies the GAG composition in the palatal shelves of Wistar rat fetuses at various periods of palatogenesis where clefts were induced experimentally using 5-fluoro-2-deoxyuridine (FUDR). For both normal and cleft palatal shelves, hyaluronan, heparan sulphate and chondroitin-4-sulphate were detected but not dermatan sulphate or chondroitin-6-sulphate. Throughout the period of cleft development studied, the total amount of GAG was significantly decreased (by approx. 30%) compared with normal development, this decrease being particularly marked at a time equivalent to post-elevation during normal development (approx. 75%). Furthermore, and unlike normal palatogenesis, no significant differences were recorded between the anterior and posterior parts of the palatal shelves during cleft formation. As for normal palatogenesis, however, the percentages of each GAG were not altered at any stage. The findings are consistent with the view that suppression of GAG biosynthesis is related to the development of cleft palate in FUDR-treated rat fetuses and can therefore be interpreted as providing evidence of a role for the mesenchymal glycoconjugates in shelf elevation during normal palatogenesis.