Isotretinoin effect on alveolar repair after exodontia-a study in rats.
Summary of "Isotretinoin effect on alveolar repair after exodontia-a study in rats."
To evaluate isotretinoin effect on alveolar repair after tooth extraction of maxillary incisor and serum calcium levels in rats. STUDY
Wistar rats (60-day-old) were assigned to control (CG, n = 12) and experimental (EG, n = 20) groups. EG received daily isotretinoin (7.5 mg/kg) for 30 days before surgery and until euthanasia, 7, 21, 28, or 90 days after tooth extraction. Blood was collected in the EG to analyze serum calcium levels before isotretinoin administration and at euthanasia. Right hemimaxillae underwent histological examination, and the slides were stained with HE and analyzed by descriptive light microscopy.
There was acceleration in the process of alveolar repair in the EG at all time points when compared to controls. Serum calcium levels showed a statistically significant decrease between first and second blood collection at days 21, 28, and 90.
Daily isotretinoin in a dose corresponding to the treatment of cystic acne accelerated alveolar repair.
Department of Oral and Maxillofacial Surgery and Maxillofacial Prosthodontics, School of Dentistry, Universidade Federal de Pelotas (UFPEL), Rua Gonçalves Chaves, 3.657/401 B, Pelotas, Rio Grande do Sul, Brazil, CEP 96015-560-Bairro: Centro, betabergoli@
This article was published in the following journal.
Name: Oral and maxillofacial surgery
- PubMed Source: http://www.ncbi.nlm.nih.gov/pubmed/20658349
- DOI: http://dx.doi.org/10.1007/s10006-010-0235-8
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Medical and Biotech [MESH] Definitions
Inbred rats derived from Sprague-Dawley rats and used for the study of salt-dependent hypertension. Salt-sensitive and salt-resistant strains have been selectively bred to show the opposite genetically determined blood pressure responses to excess sodium chloride ingestion.
Factors that modify the effect of the putative causal factor(s) under study.
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The reconstruction of a continuous two-stranded DNA molecule without mismatch from a molecule which contained damaged regions. The major repair mechanisms are excision repair, in which defective regions in one strand are excised and resynthesized using the complementary base pairing information in the intact strand; photoreactivation repair, in which the lethal and mutagenic effects of ultraviolet light are eliminated; and post-replication repair, in which the primary lesions are not repaired, but the gaps in one daughter duplex are filled in by incorporation of portions of the other (undamaged) daughter duplex. Excision repair and post-replication repair are sometimes referred to as "dark repair" because they do not require light.
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