Effect of diabetes on collagen metabolism and hypoxia in human gingival tissue: a stereological, histopathological, and immunohistochemical study.


Journal

Biotechnic & histochemistry : official publication of the Biological Stain Commission
ISSN: 1473-7760
Titre abrégé: Biotech Histochem
Pays: England
ID NLM: 9107378

Informations de publication

Date de publication:
Jan 2019
Historique:
pubmed: 16 10 2018
medline: 2 4 2019
entrez: 16 10 2018
Statut: ppublish

Résumé

Diabetes mellitus and periodontitis are chronic inflammatory diseases that disrupt soft tissue metabolism. The diseases separately or together increase apoptosis in gingival fibroblast cells and reduce cell renewal. We investigated the effects of diabetes and periodontitis on the composition and structure of gingival connective tissue. We used gingival biopsies from 16 healthy individuals (control group, C), 16 type 2 diabetic patients with chronic periodontitis (diabetes + periodontitis group, D + P) and 16 healthy chronic periodontitis patients (periodontitis group, P). Biopsies were obtained under local anesthesia. Clinical attachment level (CAL), gingival index (GI) and plaque index (PI) were measured prior to gingival biopsies. Fibroblast cells were counted stereologically. Inflammatory cells were counted histomorphometrically. Hypoxia-inducible factor (HIF)-1α, lysyl hydroxylase (PLOD-2), neutrophil collagenase (MMP-8), and vascular endothelial growth factor (VEGF) levels were evaluated immunohistochemically. CAL, GI and PI for the C group were lower than for the other groups (p < 0.05). Fibroblast cell counts were lower for the D + P group than for the other groups (p < 0.05). Diabetes increased inflammatory cell numbers in the D and D + P groups compared to the C and P groups. MMP-8 levels were higher for the D + P group than for the other groups. VEGF was elevated in both the P and D + P groups compared to the C group, while HIF-1α and PLOD-2 levels were comparable. Diabetes increased tissue destruction and inflammation, and decreased fibroblast cell numbers without affecting collagen crosslinking and HIF-1α levels.

Identifiants

pubmed: 30317872
doi: 10.1080/10520295.2018.1508745
doi:

Substances chimiques

HIF1A protein, human 0
Hypoxia-Inducible Factor 1, alpha Subunit 0
VEGFA protein, human 0
Vascular Endothelial Growth Factor A 0
Collagen 9007-34-5
PLOD2 protein, human EC 1.14.11.4
Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase EC 1.14.11.4
Matrix Metalloproteinase 8 EC 3.4.24.34

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

65-73

Auteurs

H Balci Yuce (H)

a Departments of Periodontology , Gaziosmanpaşa University , Tokat , Turkey.

Ö Karatas (Ö)

a Departments of Periodontology , Gaziosmanpaşa University , Tokat , Turkey.

F Tulu (F)

a Departments of Periodontology , Gaziosmanpaşa University , Tokat , Turkey.

A Altan (A)

b Oral and Maxillofacial Surgery , Gaziosmanpaşa University , Tokat , Turkey.

F Gevrek (F)

c Histology and Embryology, Faculty of Medicine , Gaziosmanpaşa University , Tokat , Turkey.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH