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Trigeminal nitric oxide synthase expression correlates with new bone formation during distraction osteogenesis.

作者信息

de Albuquerque Rubens Ferreira, Aparecida Del Bel Elaine, Brentegani Luiz Guilherme, Moura de Oliveira Maria Tereza, Mardegan Issa João Paulo

机构信息

Faculty of Dentistry of Ribeirão Preto, University of São Paulo, Av. Café S/N, CEP 14040-904, Ribeirão Preto, São Paulo, Brazil.

出版信息

Calcif Tissue Int. 2008 Apr;82(4):309-15. doi: 10.1007/s00223-008-9107-8. Epub 2008 Mar 12.

DOI:10.1007/s00223-008-9107-8
PMID:18330484
Abstract

Nitric oxide synthase (NOS) has been reported to be involved with both bone healing and bone metabolism. The aim of this study was to test the null hypothesis that there is no correlation between new bone formation during mandibular distraction osteogenesis and NOS expression in the trigeminal ganglion of rats. Newly formed tissue during distraction osteogenesis and trigeminal NOS expression measured by the NADPH-diaphorase (NADPH-d) reaction were evaluated in 72 male Wistar rats by histomorphometric and histochemical methods. In animals submitted to 0.5 mm/day distraction osteogenesis, the percentage of bone tissue was higher in the basal area of the mandibles compared with the center and significantly increased through the experimental periods (P < 0.05). At the sixth postoperative week, the difference in bone formation between the continuous and acute distraction osteogenesis groups was the highest. Significant correlation between new bone formation by distraction osteogenesis and NADPH-d-reactive neurons was found, varying according to neuronal cell size (r = -0.6, P = 0.005, small cells strongly stained; r = 0.5, P = 0.018, large cells moderately stained). The results suggest that NOS may play a role in the bone healing process via neurogenic pathways, and the phenomenon seems to be neuronal cell morphotype-dependent. Further studies are now warranted to investigate the mechanistic link between the expression of trigeminal NOS and mandibular new bone formation by distraction osteogenesis.

摘要

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