Cellular profile of primary molars with pulp necrosis after treatment with antibiotic paste.
Lúcia de Fátima Almeida de Deus MouraMarina de Deus Moura de LimaCacilda Castelo Branco LimaAna Victória Lopes BandeiraMarcoeli Silva de MouraAirton Mendes Conde JúniorMarcia Dos Santos RizzoPublished in: International journal of experimental pathology (2018)
The interradicular region of primary molars is permeated by many foramina, channels and accessories that connect the pulp cavity with the periapical tissues anatomically. Thus, pulp decomposition products or drugs used in endodontic treatment can trigger inflammatory reactions. The aim of this study was to evaluate the blood cell profile of the alveolar region after extraction of primary molars treated with CTZ paste. Forty-eight primary molars were selected with clinical and radiographic signs of extraction. The sample was divided into three groups with 16 teeth each: Group 1-healthy teeth; Group 2-untreated decayed teeth; and Group 3-teeth treated with CTZ paste. Immediately after the extraction, blood from the interface of the tooth socket was collected and smears were performed for further evaluation. The slides were stained by the Fast Panoptic® method and analysed by two previously trained examiners who counted the leucocytes in sets of 100 cells/slide, differentiating them into neutrophils, lymphocytes, monocytes, eosinophils and basophils. The data were analysed statistically by the MANOVA test. The blood samples from Group 2 differed significantly from Group 1 samples for all classes of leucocytes, except basophils, with higher average for lymphocytes (62.56), monocytes (7.81) and eosinophils (2.31). For Group 3, there was a relative difference (P < 0.05) to Group 2, of monocytes and eosinophils values. The blood cellularity interface in the tooth socket of primary teeth treated with CTZ paste is similar to those of healthy, exfoliated teeth and physiologically different from untreated decayed teeth.
Keyphrases
- peripheral blood
- cone beam computed tomography
- dendritic cells
- magnetic resonance
- gene expression
- stem cells
- immune response
- magnetic resonance imaging
- oxidative stress
- single cell
- machine learning
- mass spectrometry
- high resolution
- mesenchymal stem cells
- drug induced
- electronic health record
- contrast enhanced
- clinical evaluation