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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/117241
Title: 
Beneficial Effects of Adiponectin on Periodontal Ligament Cells under Normal and Regenerative Conditions
Author(s): 
Institution: 
  • Univ Bonn
  • Universidade Estadual Paulista (UNESP)
  • Univ Bern
ISSN: 
2314-6745
Sponsorship: 
  • German Research Foundation (Clinical Research Unit)
  • Medical Faculty of the University of Bonn
Sponsorship Process Number: 
German Research Foundation (Clinical Research Unit)208/TP4
Abstract: 
Type 2 diabetes and obesity are increasing worldwide and linked to periodontitis, a chronic disease which is characterized by the irreversible destruction of the tooth-supporting tissues, that is, periodontium. The mechanisms underlying the association of diabetes mellitus and obesity with periodontal destruction and compromised periodontal healing are not well understood, but decreased plasma levels of adiponectin, as found in diabetic and obese individuals, might be a critical mechanistic link. The aim of this in vitro study was to examine the effects of adiponectin on periodontal ligament (PDL) cells under normal and regenerative conditions, and to study the regulation of adiponectin and its receptors in these cells. Adiponectin stimulated significantly the expression of growth factors and extracellular matrix, proliferation, and in vitro wound healing, reduced significantly the constitutive tumor necrosis factor-alpha expression, and caused a significant upregulation of its own expression. The beneficial actions of enamel matrix derivative on a number of PDL cell functions critical for periodontal regeneration were partially enhanced by adiponectin. The periodontopathogen Porphyromonas gingivalis inhibited the adiponectin expression and stimulated the expression of its receptors. In conclusion, reduced levels of adiponectin, as found in type 2 diabetes and obesity, may compromise periodontal health and healing.
Issue Date: 
1-Jan-2014
Citation: 
Journal Of Diabetes Research. New York: Hindawi Publishing Corporation, 11 p., 2014.
Time Duration: 
11
Publisher: 
Hindawi Publishing Corporation
Source: 
http://dx.doi.org/10.1155/2014/796565
URI: 
Access Rights: 
Acesso aberto
Type: 
outro
Source:
http://repositorio.unesp.br/handle/11449/117241
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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