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1.
Oral Oncol ; 102: 104524, 2020 03.
Article in English | MEDLINE | ID: mdl-32062592

ABSTRACT

Oral Mucositis is a frequent and debilitating inflammatory complication in patients with head and neck malignancies and may lead to unplanned treatment interruptions due to intense pain and dysphagia. This systematic review with meta-analysis was performed to determine the effectiveness of low-level laser therapy in preventing oral mucositis in this context. The following databases were searched through September 2018, with last search performed on May 2019, for clinical trials: MEDLINE via PubMed, Cochrane Central, Scopus, Lilacs, ISI Web of Science and SIGLE via Open Grey. From 14,525 records, 4 studies were included in the review and 3 studies were included in meta-analysis. Data from 500 patients (mean age of 53.595 and 54.14 for intervention and control groups, respectively) were analysed. Meta-analysis showed that laser therapy prevents oral mucositis incidence in 28% and 23% of cases during the third and fourth follow-up week, respectively, in comparison to a placebo-treated control group. There was no statistically significant difference the prevention of pain; dysphagia and quality of life were not analysed due to missing. Laser therapy was effective in preventing oral mucositis from the 15th to the 45th days of chemoradiotherapy. However, new primary studies with low risk of bias are needed so a higher scientific evidence can be obtained.


Subject(s)
Chemoradiotherapy/adverse effects , Head and Neck Neoplasms/therapy , Low-Level Light Therapy , Stomatitis/prevention & control , Bias , Data Analysis , Deglutition Disorders/etiology , Deglutition Disorders/prevention & control , Female , Humans , Male , Middle Aged , Pain/prevention & control , Stomatitis/etiology , Treatment Outcome
2.
Exp Toxicol Pathol ; 63(5): 473-8, 2011 Jul.
Article in English | MEDLINE | ID: mdl-20537513

ABSTRACT

This study aimed to evaluate the effect of rosuvastatin upon structural and ultrastructural aortic remodeling in a rat model of hypertension induced by NO synthase blockade. Wistar rats were divided into 4 groups: Control group (C); control treated with rosuvastatin 20mg/kg/day (CR); L-NAME group 40 mg/kg/day (LN) and L-NAME treated with rosuvastatin (LNR) (same doses). Body mass and blood pressure were measured weekly; the experiment lasted 5 weeks. L-NAME administration augmented blood pressure (BP) in the LN group in comparison to the C group (123.3 vs. 180.5 mm Hg at week 5). In LNR rats, rosuvastatin slightly attenuated BP rise, but it had no effect on the BP of CR group. Intima and media thickening of the thoracic aorta were observed in the LN group, and increased elastic fiber content as well. Rosuvastatin prevented all these alterations as seen in the LNR group. Ultrastructural changes due to L-NAME intake (intracellular vesicles and altered membrane morphology in endothelial cells, extracellular matrix deposition, and cytoplasmatic projections from smooth muscle cells toward the internal elastic lamina) were also prevented by rosuvastatin. All in all, rosuvastatin administration is capable of attenuating ultrastructural aortic wall remodeling in NO-deficient rats despite small changes in blood pressure.


Subject(s)
Aorta, Thoracic/drug effects , Fluorobenzenes/pharmacology , Hydroxymethylglutaryl-CoA Reductase Inhibitors/pharmacology , Hypertension/pathology , Nitric Oxide/deficiency , Pyrimidines/pharmacology , Sulfonamides/pharmacology , Animals , Aorta, Thoracic/metabolism , Aorta, Thoracic/ultrastructure , Blood Pressure/drug effects , Disease Models, Animal , Endothelial Cells/drug effects , Endothelial Cells/metabolism , Endothelial Cells/ultrastructure , Fluorobenzenes/therapeutic use , Hydroxymethylglutaryl-CoA Reductase Inhibitors/therapeutic use , Hypertension/drug therapy , Hypertension/metabolism , Immunohistochemistry , Lipids/blood , Microscopy, Electron, Transmission , NG-Nitroarginine Methyl Ester/pharmacology , Nitric Oxide Synthase Type III/antagonists & inhibitors , Pyrimidines/therapeutic use , Rats , Rats, Wistar , Rosuvastatin Calcium , Sulfonamides/therapeutic use , Tunica Intima/drug effects , Tunica Intima/metabolism , Tunica Intima/ultrastructure
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