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1.
J Periodontol ; 75(2): 306-15, 2004 Feb.
Article in English | MEDLINE | ID: mdl-15068120

ABSTRACT

BACKGROUND: A hypothesis of an increased risk for destructive periodontal diseases due to psychological stress has long been promoted. However, the research on stress and periodontal disease is still in its infancy. One of the reasons is thought to be that there is no suitable animal model for investigating the relationship. METHODS: One hundred male Wistar rats were included. A nylon ligature was placed around the second right maxillary molars. The animals were then divided into group S, exposed to a restraint stress for 12 hours/day for up to 10 days, and group N, controls. Ten animals were sacrificed on days 2, 4, 6, 8, and 10. Blood samples were taken, and the blood glucose level and the concentrations of adrenocorticotropic hormone, corticosterone, and adrenaline were measured as the markers of stress. The atrophies of the thymus and the spleen were measured. The furcation area of the second maxillary molars was examined histologically and histometrically. RESULTS: In group S, all values of stress markers were increased, and the thymus and the spleen were atrophied. Whereas group N showed only slight alveolar bone resorption, a marked alveolar bone resorption occurred in group S between days 8 and 10. An increase in beaded nerve terminals occurred around the vessels in the furcation area of group S. CONCLUSION: The results of the present study suggest that the restraint stress modulates the progression of periodontal inflammation and that this rat model is suitable for investigating the association between stress and periodontal disease.


Subject(s)
Periodontitis/physiopathology , Restraint, Physical , Stress, Physiological/physiopathology , Adrenocorticotropic Hormone/blood , Alveolar Bone Loss/physiopathology , Animals , Atrophy , Blood Glucose/analysis , Corticosterone/blood , Disease Models, Animal , Disease Progression , Epinephrine/blood , Furcation Defects/physiopathology , Male , Random Allocation , Rats , Rats, Wistar , Spleen/pathology , Stress, Physiological/blood , Stress, Psychological/blood , Stress, Psychological/physiopathology , Thymus Gland/pathology
2.
J Periodontal Res ; 39(3): 158-67, 2004 Jun.
Article in English | MEDLINE | ID: mdl-15102044

ABSTRACT

OBJECTIVE: The purpose of this study was to evaluate the relationship between the clinical changes after non-surgical periodontal therapy and interleukin 1 (IL-1) in gingival crevicular fluid (GCF) and gingival tissues from patients with chronic periodontitis. BACKGROUND: The inflammatory responses mediated by IL-1 play an important role in periodontal tissue destruction. Although numerous studies have attempted to elucidate the dynamic movement involved in chronic periodontitis, the results have often conflicted. Such discrepancies may have been due to the inability to determine clinical disease activity. METHODS: Seven patients with chronic periodontitis were examined. The severity of periodontal inflammation was expressed using clinical parameters before and after a scaling and root planing (SRP) procedure. The amounts and concentrations of IL-1alpha, IL-1beta and IL-1 receptor antagonist in GCF were measured by enzyme-linked immunosorbent assay (ELISA) and IL-1 activity index was calculated. A needle biopsy in matching gingival tissues was also performed before and after the SRP procedure. The localization and mRNA expression of IL-1beta were determined using histological methods. RESULTS: Clinical parameters improved slightly after the SRP procedure. Only the probing pocket depth (PPD) was reduced significantly (p < 0.05). However, the amount of IL-1beta in GCF was slightly increased. The localization and mRNA expression of IL-1beta could still be observed after the SRP procedure. Therefore, none of the clinical parameters showed a high sensitivity or specificity for evaluating subgingival inflammation. CONCLUSION: These observations suggest that IL-1 is effective for evaluating in detail the state of subgingival inflammation.


Subject(s)
Dental Scaling , Interleukin-1/biosynthesis , Periodontitis/metabolism , Periodontitis/therapy , Adult , Chronic Disease , Female , Gingiva/metabolism , Gingival Crevicular Fluid/metabolism , Humans , Immunohistochemistry , In Situ Hybridization , Male , Middle Aged , RNA, Messenger/analysis , RNA, Messenger/biosynthesis , Receptors, Interleukin-1/antagonists & inhibitors
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