Evaluation of the stability of immediate placed dental maxillary implant in fresh extracted socket versus delayed placed implant

Document Type : Original Article

Authors

1 B.D.S, 2010 G. Faculty of Dental Medicine, Al-Mansoura University, Dentist at Egyptian Ministry of Health

2 Professor of Oral and Maxillofacial Surgery Department, Dean of Faculty of Dental Medicine, Cairo Boys, Al-Azhar University

3 Lecturer of Oral and Maxillofacial Surgery Department, Faculty of Dental Medicine, Cairo Boys, Al-Azhar University

Abstract

Introduction: Botulinum toxin A (BoNTA) has been used for treating hyperfunction of various glands such as sweat, lacrimal, and salivary glands. However, the long-term histological sequences are largely unknown. Objectives: The present study is to evaluate the histological and ultrastructural effects of BoNTA on submandibular salivary gland (SSG). Methods: Sixty male albino rats received 0.1 ml of either saline (control group) or BoNTA (BoNTA group) injection in the right SSGs. The rats were terminated at 2, 4 and 12 weeks after the injection. The harvested SSGs were embedded and sectioned at 4-5 µm and stained with H&E for histological study. Ultrathin sections (60-90nm) were cut from1 mm3 pieces harvested from the center of SSGs, and mounted on copper grids for ultrastructural study using transmission electron microscope (TEM). Results: All control SSGs showed normal acinar cells with rounded nuclei and regular striated ducts (SD) with characteristic basal striations. By TEM, acinar cells exhibited rounded nuclei, mitochondria, and secretory granules at cytoplasm. Numerous mitochondria presented in SD. Compared with these features, 2-week BoNTA-injected SSGs showed loss of basal striations. Examination by TEM revealed irregular nuclei of acinar cells and SD, and swollen mitochondria. In 4-week SSGs, some acini and ducts lost their spherical fashion and in some areas, these structures disappeared. Ruptured mitochondria were observed in acini and SD by TEM. However, all 12-week BoNTA-injected SSGs seemed to have similar structures to those of control SSGs. By using scoring system for semi-quantifying the histological structural changes of BoNTA-injected SSGs, 2- and 4-week BoNTA-injected SSGs showed significantly higher scores as compared with their control counterparts. However, no significant score difference was found between 12-week BoNTA-injected and control SSGs. Conclusions: Although application of BoNTA results in significant changes in histological structures and ultrastructures of SSGs, these detrimental effects seems to be transient, and the major recovery occurs after 3 months. Thus, BoNTA can be used for treating SSG hyperfunction.