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1.
J. appl. oral sci ; 27: e20180108, 2019. tab, graf
Article in English | LILACS, BBO | ID: biblio-975873

ABSTRACT

Abstract Objective: This study aims to evaluate the clinical and biochemical (oxidative stress and pro-inflammatory mediators) effects of the gaseous ozone use accompanied by scaling and root planning (SRP) in periodontal treatment. Material and Methods: The study population consisted of 40 patients with chronic periodontitis (CP) randomly sorted into two groups of 20. The experimental group received SRP plus 3 watts gaseous ozone in two separate applications five days apart, whereas the control group received SRP plus placebo. Clinical periodontal parameters were assayed and saliva samples were taken before the initial and one month after the second treatment. Periodontal examination assessed plaque index (PI), gingival index (GI), probing depth, and clinical attachment level (CAL). Total antioxidant status (TAS), total oxidant status (TOS), nitric oxide (NO), 8-hydroxy-2'-deoxyguanosine (8-OHdG), myeloperoxidase (MPO), glutathione (GSH), malondialdehyde (MDA), and transforming growth factor-beta (TGF-β) levels were evaluated from saliva samples. Results: Changes following treatment in PI, GI, probing depth, and CAL scores were similar for both groups (p>0.05). Of note, TGF-β levels were observed to be higher in the treatment group than in controls (p<0.05). Changes in 8-OHdG, TAS, TOS, NO, MPO, GSH and MDA levels, however, were not significantly different between groups (p>0.05). Conclusion: The findings of this study indicate that SRP plus gaseous ozone versus SRP alone does not correlate to a significant improvement in periodontal recovery.


Subject(s)
Humans , Male , Female , Adult , Oxidants, Photochemical/therapeutic use , Ozone/therapeutic use , Root Planing/methods , Chronic Periodontitis/therapy , Saliva/chemistry , Time Factors , Enzyme-Linked Immunosorbent Assay , Periodontal Index , Dental Plaque Index , Reproducibility of Results , Transforming Growth Factor beta/analysis , Treatment Outcome , Oxidants/antagonists & inhibitors , Peroxidase/analysis , Statistics, Nonparametric , Deoxyguanosine/analysis , Deoxyguanosine/analogs & derivatives , Chronic Periodontitis/pathology , Glutathione/analysis , Malondialdehyde/analysis , Middle Aged , Nitric Oxide/analysis , Antioxidants/analysis
2.
Acta cir. bras ; 31(11): 730-735, Nov. 2016. tab, graf
Article in English | LILACS | ID: biblio-827659

ABSTRACT

ABSTRACT PURPOSE: To assess and compare the histopathological effects of ozone therapy and/or methylprednisolone (MPS) treatment on regeneration after crush type sciatic nerve injury. METHODS: Forty Sprague-Dawley male rats were randomly allocated into four groups. Four groups received the following regimens intraperitoneally every day for 14 days after formation of crush type injury on sciatic nerve: Group I: ozone (20mcg/ml); Group II: methylprednisolone (2mg/kg); Group III: ozone (20 mcg/ml) and methylprednisolone (2mg/kg); Group IV: isotonic saline (0.9%). The histomorphological evaluation was made after biopsies were obtained from the sites of injury. RESULTS: Significant differences were noted between groups in terms of degeneration (p=0.019), nerve sheath cell atrophy (p=0.012), intraneural inflammatory cellular infiltration (p=0.002), perineural granulation tissue formation (p=0.019), perineural vascular proliferation (p=0.004), perineural inflammatory cellular infiltration (p<0.001) and inflammation in peripheral tissue (p=0.006). Degeneration was remarkably low in Group III, while no change in nerve sheath cell was noted in Group II. CONCLUSION: The combined use of methylprednisolone and ozone treatment can have beneficial effects for regeneration after crush type nerve injury.


Subject(s)
Animals , Male , Rats , Oxidants, Photochemical/therapeutic use , Ozone/therapeutic use , Sciatic Nerve/injuries , Methylprednisolone/therapeutic use , Peripheral Nerve Injuries/drug therapy , Nerve Regeneration/drug effects , Oxidants, Photochemical/administration & dosage , Ozone/administration & dosage , Sciatic Nerve/drug effects , Wound Healing/drug effects , Methylprednisolone/administration & dosage , Random Allocation , Rats, Sprague-Dawley , Recovery of Function/drug effects , Peripheral Nerve Injuries/physiopathology , Inflammation , Nerve Crush
3.
Acta cir. bras ; 31(4): 256-263, Apr. 2016. graf
Article in English | LILACS | ID: lil-781329

ABSTRACT

PURPOSE: To investigate the effect of medical ozone treatment on the experimental acute distal colitis in rats. METHODS: Eighteen rats were randomly distributed into three equal groups; control, acute distal colitis (ADC) without and with medical ozone treatment. Rats in the control group were taken saline. ADC was performed by rectal way with 4% acetic acid in groups 2 and 3, and the group 3 was treated with medical ozone for three weeks both rectally and intraperitoneally. At the twenty second day the distal colons samples were obtained for malondialdehyde and myeloperoxidase, blood samples were obtained to measure the levels of TNF-α and IL-1β levels. Histolopatological examination was evaluated with Ki-67, IL-1β and VEGF immunostaining densities. RESULTS: There was significant increase in tissue MDA, MPO activity, TNF-α and IL-1β after ozone administration. There was also a significant difference at immunostaining densities of histopathological examination. CONCLUSIONS: Medical ozone treatment ameliorated the experimental acute distal colitis induced by acetic acid in rats. Its possible effect is by means of decreasing inflammation, edema, and affecting the proliferation and the vascularization.


Subject(s)
Animals , Male , Oxidants, Photochemical/therapeutic use , Ozone/therapeutic use , Colitis, Ulcerative/drug therapy , Time Factors , Immunohistochemistry , Colitis, Ulcerative/pathology , Random Allocation , Acute Disease , Reproducibility of Results , Tumor Necrosis Factor-alpha/blood , Treatment Outcome , Rats, Wistar , Colon/pathology , Peroxidase/analysis , Acetic Acid , Vascular Endothelial Growth Factor A/analysis , Disease Models, Animal , Interleukin-1beta/blood , Malondialdehyde/analysis
4.
Article in English | IMSEAR | ID: sea-139878

ABSTRACT

Background: The development of periodontal disease has been thought to be associated with several restricted members of the oral anaerobic species, such as black-pigmented Porphyromonas species and Actinobacillus actinomycetemcomitans (Aa), in the subgingival environment. Apart from bacteria, certain viruses and fungi that are associated with periodontal disease are also present in the subgingival plaque . Materials and Methods: A randomized, double-blind, crossover split-mouth design was performed. A total of 16 patients suffering from generalized chronic periodontitis were selected for the study. The study period of 18 days was divided into two time-intervals, i.e. baseline (0 days) to 7 th day, with a washout period of 4 days followed by a second time interval of 7 days. The use of ozone and chlorhexidine gluconate (CHX) irrigation was randomized. Both the patient and the clinician evaluating the clinical parameters were blinded regarding the type of irrigation used. Results: The interpretation of clinical and microbial data is from baseline to 7 th day. A higher percentage of plaque index (12%), gingival index (29%) and bleeding index (26%) reduction was observed using ozone irrigation as compared to chlorhexidine. The percentile reduction of Aa (25%) using ozone was appreciable as compared to no change in Aa occurrence using chlorhexidine. By using O 3 and chlorhexidine, there was no antibacterial effect on Porphyromonas gingivalis (Pg) and Tannerella forsythensis. The antifungal effect of ozone from baseline (37%) to 7 th day (12.5%) was pronounced during the study period, unlike CHX, which did not demonstrate any antifungal effect. Conclusion: Ozone may be considered as an alternative management strategy due to its powerful ability to inactivate microorganisms. Also, there is growing evidence that ozone can be employed as a useful therapeutic agent in both dentistry and medicine.


Subject(s)
Aggregatibacter actinomycetemcomitans/drug effects , Aggressive Periodontitis/drug therapy , Anti-Infective Agents, Local/administration & dosage , Anti-Infective Agents, Local/therapeutic use , Antifungal Agents/administration & dosage , Antifungal Agents/therapeutic use , Antiviral Agents/administration & dosage , Antiviral Agents/therapeutic use , Bacteroides/drug effects , Candida albicans/drug effects , Chlorhexidine/administration & dosage , Chlorhexidine/therapeutic use , Chronic Periodontitis/drug therapy , Cross-Over Studies , Cytomegalovirus/drug effects , Dental Plaque Index , Double-Blind Method , Gingival Hemorrhage/drug therapy , Herpesvirus 1, Human/drug effects , Herpesvirus 2, Human/drug effects , Herpesvirus 4, Human/drug effects , Humans , Oxidants, Photochemical/administration & dosage , Oxidants, Photochemical/therapeutic use , Ozone/administration & dosage , Ozone/therapeutic use , Periodontal Index , Porphyromonas gingivalis/drug effects , Therapeutic Irrigation , Time Factors , Time Factors
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