Effect of enamel matrix protein derivative on healing of surgical supra-infrabony periodontal defects in the rat molar: a histomorphometric study.

BACKGROUND: Enamel matrix protein derivative (EMD) has proven to enhance periodontal regeneration in human and animal studies. The present histomorphometric study evaluated healing of combined supra-infrabony periodontal defects with EMD. METHODS: The study comprised two groups of 10 Wistar rats each, 7 to 8 months old. Bony defects were created on the mesial aspect of the mesial root of the first maxillary molar. The root surface was planed and 24% EDTA gel applied for 2 minutes and then rinsed with water. In the study group, EMD was applied, and in the control group, only propylene glycol alginate was applied. Animals were sacrificed 12 weeks after surgery, and block sections were removed, demineralized, and embedded in paraffin. For histomorphometric analysis, three sections from the central area of the defect were selected. Root, surgical defect, epithelial attachment, sulcus, supracrestal connective tissue, ankylosis, and the length and area of new cementum and new bone were measured. RESULTS: No statistically significant differences between the two groups were found for root and defect measures. The remaining parameters were calculated as a percentage of the defect. In the study group, smaller gingival recession (P = 0.05), deeper gingival sulcus (P = 0.05), and shorter junctional epithelium (P = 0.01) were found. New cementum was observed in the study group only (P = 0.02). Ankylosis was six times larger in the control group but not statistically significant. New bone formation was similar in both groups. CONCLUSION: Enamel matrix protein derivative enhanced periodontal healing in this model by reducing gingival recession and junctional epithelium along the root surface and enhancing the formation of new cementum.

Tetracycline impregnation delays collagen membrane degradation in vivo.

BACKGROUND: Guided tissue and bone regeneration using bioabsorbable collagen membranes is a common practice. Collagen promotes progenitor cell adhesion, chemotaxis, homeostasis, and physiologic degradation with low immunogenicity, which makes it an ideal material for barrier preparation. Collagen membranes have to maintain integrity for a proper time, thus ensuring successful cell exclusion. Early collagen membrane degradation is detrimental for the success of regenerative procedures. This in vivo study was conducted to evaluate the effect of soaking collagen membranes in different tetracycline hydrochloride (TCN) concentration solutions on its degradation. METHODS: Five mm disks of collagen membrane were soaked in either 100 mg/ml TCN (group 100) or 50 mg/ml TCN (group 50); a group of non-treated disks served as controls. All disks were labeled with aminohexanoyl-biotin-N-hydroxy-succinimide ester (biotin) and implanted in rat calvaria bone. Block sections were taken after 3 weeks and histological slides stained with horseradish peroxidase (HRP) to detect remnants of biotinylated collagen. Staining intensity was analyzed by image-analysis software taking quadruplicate measurements of a 500 microm2 area each. Data were analyzed using analysis of variance (ANOVA) with repeated measures and paired t test with Bonferroni correction. RESULTS: Staining intensity of membranes in group 100 was > 5-fold higher than the control while group 50 exhibited > 11-fold higher intensity than the control and > 2.5-fold higher than the 100. All of these differences were statistically significant (P < 0.001). CONCLUSION: Soaking collagen membranes in 50 mg/ml TCN solution is a useful, practical, and simple tool to slow membrane degradation.