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Micrometric measurement of the density of stained odontoblast processes
Author(s) -
Alicia Kohli,
Stella Maris Pezzotto,
Graciela García,
Leonor Poletto
Publication year - 2011
Publication title -
biocell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.182
H-Index - 27
eISSN - 1667-5746
pISSN - 0327-9545
DOI - 10.32604/biocell.2011.35.051
Subject(s) - staining , pulp (tooth) , dentinal tubule , odontoblast , chemistry , collagenase , stain , anatomy , dentin , vital stain , h&e stain , dentistry , pathology , biology , medicine , biochemistry , enzyme
UNLABELLEDThe embryological, structural and functional unit of the dentine-pulp complex shares the odontoblast, located in the border of the dentine pulp, with basal nuclei and organelles. The odontoblast process emerges from its apical pole. It is formed by microtubules, microfilaments and vesicles covered by membranes penetrating the dentinal tubules, isolated from the inter-tubular matrix, along the extent of the dentine. The objective of this study was to evaluate the efficacy of three staining techniques: hematoxylin-eosin, periodic acid-Schiff and Schmorl, by staining the process, from beginning to end, and compare the results with the erosion technique. Thirty human teeth were employed in the trial; after their extraction the pulp was fixated, the pieces demineralized in nitric acid at 8%, the collagen filaments eliminated with Type II Collagenase, the tissue was stained, and the measurements were made. The portions with no pulp were prepared with the erosion technique.RESULTSComparing the best results obtained by staining with the values obtained with the erosion technique, the former showed lower values.CONCLUSIONStaining techniques show lower density of the staining processes compared with the dentinal tubules in the erosion technique.

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