Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 4 de 4
Filter
Add more filters










Database
Language
Publication year range
1.
J Dent Res ; 92(8): 735-9, 2013 Aug.
Article in English | MEDLINE | ID: mdl-23694931

ABSTRACT

Oxidative stress is associated with age-related reactions. The anti-oxidative effects of a reduced form of co-enzyme Q10 (rCoQ10) suppress oxidative stress, which may contribute to the prevention of age-related inflammatory reactions. We examined the effects of topically applied rCoQ10 on periodontal inflammatory reactions in a rat aging model. Male Fischer 344 rats, 2 (n = 6) and 4 mos (n = 18) of age, were used. All of the two-month-old rats and 6 of the four-month-old rats were sacrificed and 12 remaining four-month-old rats received topically applied ointment with or without 1% rCoQ10 on the gingival surface until they reached 6 mos of age. The rats showed an age-dependent increase in circulating oxidative stress. RCoQ10 decreased oxidative DNA damage and tartrate-resistant acid-phosphatase-positive osteoclasts in the periodontal tissue at 6 mos of age as compared with the control. The same conditions lowered gene expression of caspase-1 and interleukin-1ß in the periodontal tissue. Furthermore, Nod-like receptor protein 3 inflammasomes were less activated in periodontal tissues from rCoQ10-treated rats as compared with the control rats. Our results suggest that rCoQ10 suppresses age-related inflammatory reactions and osteoclast differentiation by inhibiting oxidative stress.


Subject(s)
Aging/drug effects , Electron Transport Chain Complex Proteins/pharmacology , Periodontium/drug effects , Ubiquinone/analogs & derivatives , Vitamins/pharmacology , 8-Hydroxy-2'-Deoxyguanosine , Acid Phosphatase/analysis , Actins/drug effects , Age Factors , Alveolar Process/drug effects , Alveolar Process/pathology , Animals , Antioxidants/pharmacology , Apoptosis Regulatory Proteins , CARD Signaling Adaptor Proteins , Carrier Proteins , Caspase 1/drug effects , Cytoskeletal Proteins/drug effects , DNA Damage/drug effects , Deoxyguanosine/analogs & derivatives , Deoxyguanosine/analysis , Deoxyguanosine/blood , Gingiva/drug effects , Gingiva/pathology , Inflammasomes/drug effects , Interleukin-1beta/drug effects , Isoenzymes/analysis , Male , Models, Animal , NF-kappa B/drug effects , NLR Family, Pyrin Domain-Containing 3 Protein , Osteoclasts/drug effects , Oxidative Stress/drug effects , Periodontium/pathology , Random Allocation , Rats , Rats, Inbred F344 , Receptors, Cytoplasmic and Nuclear/drug effects , Tartrate-Resistant Acid Phosphatase , Ubiquinone/blood , Ubiquinone/pharmacology
2.
J Periodontal Res ; 48(2): 177-83, 2013 Apr.
Article in English | MEDLINE | ID: mdl-22891771

ABSTRACT

BACKGROUND AND OBJECTIVE: Electric current is used to promote wound healing. However, it is unclear whether electrical stimulation contributes to gingival tissue remodeling. This study examined the effects of electrical stimulation on gingival tissue remodeling in a rat periodontitis model. MATERIAL AND METHODS: Male Wistar rats (n = 28, 8 wks of age) were divided into four groups of seven rats each. The control group did not receive any treatment for 6 wks. In the other groups, periodontitis was ligature-induced for 4 wks. After 4 wks, the rats with periodontitis were given daily electrical stimulation of 0, 50 or 100 µA for 2 wks. RESULTS: The periodontitis group stimulated with 0 µA showed a higher density of polymorphonuclear leukocytes and a lower density of collagen in gingival tissue compared with the control group (p < 0.05). The two remaining groups treated with 50 or 100 µA of electrical stimulation exhibited a lower density of polymorphonuclear leukocytes (p < 0.05) and a higher density of collagen than the group stimulated with 0 µA (p < 0.05). They also showed higher expression of fibroblast growth factor-2 than the group treated with 0 µA of electrical stimulation (p < 0.05). CONCLUSION: Electric stimulation may offer a novel approach to promote gingival tissue remodeling in periodontal lesions.


Subject(s)
Electric Stimulation Therapy/methods , Gingiva/physiopathology , Periodontitis/therapy , Alveolar Bone Loss/pathology , Animals , Collagen/ultrastructure , Connective Tissue/pathology , Epithelial Attachment/pathology , Fibroblast Growth Factor 2/analysis , Fibroblasts/pathology , Gingiva/pathology , Leukocyte Count , Male , Matrix Metalloproteinase 3/analysis , Matrix Metalloproteinase 8/analysis , Matrix Metalloproteinase 9/analysis , Matrix Metalloproteinase Inhibitors/analysis , Neutrophils/pathology , Osteoblasts/pathology , Periodontitis/pathology , Random Allocation , Rats , Rats, Wistar , Tissue Inhibitor of Metalloproteinase-1/analysis , Tissue Inhibitor of Metalloproteinase-2/analysis , Tissue Inhibitor of Metalloproteinase-3/analysis , Tooth Cervix/pathology , Wound Healing/physiology
3.
J Periodontal Res ; 47(2): 159-64, 2012 Apr.
Article in English | MEDLINE | ID: mdl-21923677

ABSTRACT

BACKGROUND AND OBJECTIVE: Inorganic polyphosphate [poly(P)] is a biopolymer found in almost all cells and tissues, and which promotes tissue remodeling. However, there is limited information on how poly(P) affects the connective tissue in inflamed gingiva. This study examined the effects of topical application of poly(P) on gingival connective tissue and its remodeling in a rat periodontitis model. MATERIAL AND METHODS: Male Wistar rats (n = 36, 8 wk of age) were used in this 6-wk study. The rats were divided into six groups of six rats each. The control group received no treatment. In the other groups, periodontitis was ligature-induced for 4 wk. After 4 wk, the rats with periodontitis were further divided into five groups, and were left untreated (periodontitis group) or subjected to topical application of oral rinses containing 0, 0.1, 1 or 5% poly(P) for 2 wk. RESULTS: The periodontitis and 0% poly(P) groups showed a higher density of polymorphonuclear leukocytes and a lower density of collagen in gingival tissue than the control group (p < 0.05). In contrast, groups treated with more than 1% poly(P) exhibited a lower density of polymorphonuclear leukocytes (p < 0.05) and a higher density of collagen than the periodontitis and 0% poly(P) groups (p < 0.05). A higher expression of fibroblast growth factor-2 was observed in the gingiva of rats treated with 1% poly(P) than in those treated with 0% poly(P) (p < 0.05). CONCLUSION: Topical application of poly(P) may induce connective tissue remodeling, contributing to improvement of inflamed gingiva in rats.


Subject(s)
Gingiva/drug effects , Periodontitis/drug therapy , Polyphosphates/therapeutic use , Administration, Topical , Animals , Cell Count , Collagen/drug effects , Connective Tissue/drug effects , Connective Tissue/pathology , Disease Models, Animal , Epithelial Attachment/drug effects , Epithelial Attachment/pathology , Fibroblast Growth Factor 2/drug effects , Fibroblasts/drug effects , Fibroblasts/pathology , Gingiva/enzymology , Gingiva/pathology , Leukocyte Count , Male , Matrix Metalloproteinase 2/drug effects , Matrix Metalloproteinase 3/drug effects , Matrix Metalloproteinase 9/drug effects , Mouthwashes/therapeutic use , Neutrophils/drug effects , Neutrophils/pathology , Periodontitis/enzymology , Periodontitis/pathology , Polyphosphates/administration & dosage , Random Allocation , Rats , Rats, Wistar , Tissue Inhibitor of Metalloproteinase-1/drug effects , Tissue Inhibitor of Metalloproteinase-2/drug effects , Tissue Inhibitor of Metalloproteinase-3/drug effects
4.
Neuromolecular Med ; 13(3): 197-203, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21751079

ABSTRACT

Amyloid-ß plays a causative role in Alzheimer's disease. Occlusal disharmony causes chronic psychological stress, and psychological stress increases amyloid-ß accumulation. The purpose of the present study was to investigate whether occlusal disharmony-induced psychological stress affects the accumulation of amyloid-ß and its related gene expressions in the rat hippocampus. Eight-week-old male Wistar rats (n = 18) were divided into three groups of six rats each: (1) a control group that received no treatment for 8 weeks; (2) an occlusal disharmony group that underwent cutoff maxillary molar cusps for 8 weeks; and (3) a recovered group that underwent cutoff maxillary molar cusps for 4 weeks followed by recovery for 4 weeks. Occlusal disharmony increased plasma corticosterone levels in a time-dependent manner. Levels of amyloid-ß 40 and 42, glucocorticoid receptor (Gr) protein, and cleaved caspase 3 (Casp3) as well as gene expressions of amyloid precursor protein, beta-secretase, Casp3, and Gr in the hippocampus in the occlusal disharmony group were significantly higher than those in the control group (P < 0.016). These findings were significantly improved by recovery of occlusion (P < 0.016). These results indicate that psychological stress induced by occlusal disharmony reversibly induces amyloid-ß 40 and 42 in the rat hippocampus through the glucocorticoid signal.


Subject(s)
Alzheimer Disease/etiology , Amyloid beta-Peptides/metabolism , Hippocampus/metabolism , Malocclusion/complications , Stress, Psychological/complications , Stress, Psychological/etiology , Alzheimer Disease/pathology , Amyloid beta-Peptides/genetics , Animals , Caspase 3/metabolism , Corticosterone/blood , Dental Occlusion , Hippocampus/pathology , Male , Random Allocation , Rats , Rats, Wistar , Receptors, Glucocorticoid/metabolism
SELECTION OF CITATIONS
SEARCH DETAIL
...