Archives of Oral Biology
Volume 55, Issue 7 , Pages 523-529, July 2010

Effect of nifedipine on gingival enlargement and periodontal breakdown in ligature-induced periodontitis in rats

  • Marilene Issa Fernandes

      Affiliations

    • Periodontology, Faculty of Dentistry, Federal University of Rio Grande do SulPorto Alegre, Brazil
  • ,
  • Eduardo José Gaio

      Affiliations

    • Post-Graduate Program in Dentistry, Faculty of Dentistry, Federal University of Rio Grande do Sul, Brazil
    • Corresponding Author InformationCorresponding author at: Av. Montenegro, 160/701 – CEP: 90460-160, Porto Alegre, RS, Brazil. Tel.: +55 51 32330434; fax: +55 51 32330434.
  • ,
  • Cristiano Susin

      Affiliations

    • Departments of Periodontics & Oral Biology, Medical College of Georgia School of Dentistry, Augusta, GA, USA
  • ,
  • Cassiano Kuchenbecker Rösing

      Affiliations

    • Periodontology, Faculty of Dentistry, Federal University of Rio Grande do SulPorto Alegre, Brazil
  • ,
  • Rui Vicente Oppermann

      Affiliations

    • Periodontology, Faculty of Dentistry, Federal University of Rio Grande do SulPorto Alegre, Brazil
  • ,
  • Pantelis Varvaki Rados

      Affiliations

    • Oral Pathology, Faculty of Dentistry, Federal University of Rio Grande do Sul, Porto Alegre, Brazil

Accepted 10 May 2010.

Abstract 

Objective

A recent consensus report could not find specific reports of the effect of nifedipine on the destruction of the periodontal tissues. The aim of the present study was to evaluate the effect of nifedipine on gingival enlargement and periodontal breakdown using a ligature-induced periodontitis in rats.

Materials and methods

Fifty, male, 60 days old, Wistar rats, were divided into six groups. Cotton sutures were placed around the upper second molars. Two groups of 10 rats each did not receive ligatures and were treated daily with either saline solution or nifedipine 50mg/kg/day. Two groups of 10 rats received ligatures and were also treated daily with saline solution or nifedipine 50mg/kg/day. Two additional groups (nifedipine 10 and 100mg/kg/day) were included to explore a possible dose–response relationship. Animals were euthanatised at 30 days. Internal and oral epithelium, total and inflamed connective tissue, gingival thickness and height, and bone loss were assessed histologically.

Results

Nifedipine alone was not sufficient to promote gingival enlargement or periodontal destruction in the absence of the ligature. Compared to animals with ligatures only, the group that received ligatures and nifedipine 50mg/kg/day showed significant higher estimates for total and inflamed connective tissue, gingival thickness and height. No significant differences were observed for bone loss between these experimental groups. The other dosages of nifedipine did not provide additional information.

Conclusion

Nifedipine itself did not lead to gingival enlargement in rats. In the presence of biofilm accumulation, nifedipine yielded greater gingival enlargement and periodontal inflammation, but it did not increase periodontal destruction.

Keywords: Alveolar bone loss, Gingival overgrowth, Nifedipine, Periodontitis, Rats

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PII: S0003-9969(10)00121-4

doi:10.1016/j.archoralbio.2010.05.003

Archives of Oral Biology
Volume 55, Issue 7 , Pages 523-529, July 2010