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1.
Asian Pac J Cancer Prev ; 21(5): 1235-1239, 2020 May 01.
Article in English | MEDLINE | ID: mdl-32458627

ABSTRACT

BACKGROUND: The aim of this study was to evaluate cytotoxic, mutagenic and genotoxic effects on buccal mucosa and peripheral blood cells from marijuana and tobacco smokers. METHODS: For this purpose, a total of 45 volunteers were distributed into four groups: CTRL group (control): individuals who did not smoke marijuana or tobacco (n = 11); Group M: Marijuana smokers (n = 13); Group T: Tobacco smokers (n = 13); Group M + T: Smokers of both marijuana and tobacco (n = 08). RESULTS: Smokers of both marijuana and tobacco led an increase of micronucleated cells on buccal mucosa when compared to control group. The occurrence of karyolysis showed significant changes in this group as well. The comet assay data revealed genetic damage in peripheral blood cells for all groups of smokers. CONCLUSION: In summary, our results showed that marijuana and /or tobacco are able to induce genetic damage and cytotoxicity in oral and peripheral blood cells.


Subject(s)
Blood Cells/pathology , Cannabis/adverse effects , Genomic Instability/drug effects , Mouth Mucosa/pathology , Smoke/adverse effects , Smoking/adverse effects , Adult , Blood Cells/drug effects , Case-Control Studies , Female , Follow-Up Studies , Humans , Male , Mouth Mucosa/drug effects , Prognosis , Young Adult
2.
J Trace Elem Med Biol ; 33: 37-47, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26653742

ABSTRACT

The aim of this study was to investigate if purple carrot extract is able to protect against the noxious activities induced by cadmium exposure in multiple organs of rats. For this purpose, histopathological analysis, genotoxicity and oxidative status were investigated in this setting. A total of twenty Wistar rats weighing 250g on the average, and 8 weeks age were distributed into four groups (n=5), as follows: Control group (non-treated group, CTRL); Cadmium group (Cd) and Purple carrot extract groups at 400mg/L or 800mg/L. Histopathological analysis revealed that liver from animals treated with purple carrot extract improved tissue degeneration induced by cadmium intoxication. Genetic damage was reduced in blood and hepatocytes as depicted by comet and micronucleus assays in animals treated with purple carrot extract. SOD-CuZn and cytocrome C gene expression increased in groups treated with purple carrot extract. Purple carrot extract also reduced the 8OHdG levels in liver cells when compared to cadmium group. Taken together, our results demonstrate that purple carrot extract is able to protect against cadmium intoxication by means of reducing tissue regeneration, genotoxicity and oxidative stress in multiple organs of Wistar rats.


Subject(s)
Cadmium Poisoning/drug therapy , Daucus carota/chemistry , Mutagens/toxicity , Organ Specificity , Oxidative Stress/drug effects , Plant Extracts/therapeutic use , 8-Hydroxy-2'-Deoxyguanosine , Animals , Bone Marrow Cells/drug effects , Bone Marrow Cells/metabolism , Cadmium Poisoning/metabolism , Comet Assay , Cytochromes c/metabolism , DNA Damage , Deoxyguanosine/analogs & derivatives , Deoxyguanosine/metabolism , Gene Expression Regulation/drug effects , Immunohistochemistry , Liver/drug effects , Liver/pathology , Micronucleus Tests , Plant Extracts/pharmacology , Rats, Wistar , Real-Time Polymerase Chain Reaction , Spectrometry, Mass, Electrospray Ionization , Weight Gain/drug effects
3.
Toxicol Mech Methods ; 25(7): 532-7, 2015.
Article in English | MEDLINE | ID: mdl-26062009

ABSTRACT

Several studies have shown that apple (Malus sp.) has many components able to exert chemopreventive activity. The aim of this study was to evaluate the chemopreventive potential of apple extract following medium-term oral carcinogenesis assay induced by 4-nitroquinoline 1-oxide (4NQO) by means of histopathological analysis and gene expression of antioxidant enzymes, such as CuZnSOD, MnSOD and catalase. A total of 30 male Wistar rats were distributed into five groups, as follows (n = 6 per group): Group 1 - negative control group (non-treated group); Group 2 - received 4NQO during 8 weeks in drinking water and treated with apple extract by gavage between the 1st and 4th weeks daily (initiation phase); Group 3 - received 4NQO for 8 weeks in drinking water and treated with apple extract by gavage between the 5th and 8th weeks daily (promotion phase); Group 4 - received apple extract by gavage for eight consecutive weeks only; and Group 5 - received 4NQO for 8 weeks in drinking water daily. Histopathological analysis revealed that apple extract protect oral lesions induced by 4NQO at initiation or promotion phase. Higher gene expression of CuZnSOD and MnSOD enzymes were noticed in groups treated with apple extract as well. Taken together, our results demonstrate that the apple extract is able to modulate medium-term oral carcinogenesis assay as a result of antioxidant activity.


Subject(s)
4-Nitroquinoline-1-oxide/toxicity , Anticarcinogenic Agents/pharmacology , Antioxidants/pharmacology , Carcinogens/toxicity , Malus/chemistry , Plant Extracts/pharmacology , Tongue Neoplasms/prevention & control , Animals , Drinking Water/chemistry , Epithelial Cells/pathology , Fruit/chemistry , Male , Rats , Rats, Wistar , Seeds/chemistry , Superoxide Dismutase/metabolism , Tongue Neoplasms/chemically induced
4.
Int J Food Sci Nutr ; 66(4): 439-44, 2015.
Article in English | MEDLINE | ID: mdl-25835042

ABSTRACT

The aim of this study was to investigate the phenolic composition of a natural food colourant (G8000™) as well as its effects on plasma markers after 28-day consumption by healthy individuals at a dietary dose (70 g). Parameters of total cholesterol and its fractions, triglycerides and plasma enzymes biomarkers of muscle injury were measured. Major compounds identified in G8000™ by ESI-MS showed the presence of anthocyanins, organic acids, phenolic acids as well as monosaccharides. HDL levels significantly increased from 43 ± 10.2 mg/dL to 95 ± 16.9 mg/dL. LDL levels significantly decreased from 110 ± 40.9 mg/dL to 69 ± 39 mg/dL (p < 0.001). No significant statistical differences (p > 0.05) were observed for total cholesterol, triglycerides and VLDL. After the intake, plasma enzyme CK-MB decreased from 20 ± 12.1 U/L to 10 ± 1.9 U/L while LDH levels increased from 275 ± 124.4 U/L to 317 ± 114.7 U/L (p < 0.005). No significant differences were observed for CK levels. Taken together, dietary intake of natural colourant G8000™ was able to exert beneficial effects on atherosclerosis biomarkers.


Subject(s)
Cholesterol, HDL/blood , Cholesterol, LDL/blood , Food Coloring Agents/pharmacology , Plant Extracts/blood , Plant Extracts/pharmacology , Vitis , Adult , Biomarkers/blood , Female , Food Coloring Agents/metabolism , Humans , Male , Phenols/blood , Phenols/pharmacology , Triglycerides/blood , Young Adult
5.
Toxicol Mech Methods ; 23(2): 144-9, 2013 Feb.
Article in English | MEDLINE | ID: mdl-23038986

ABSTRACT

The ketogenic diet (KD) was initially developed for the treatment of pharmacoresistant epilepsy and a possible alternative for the obesity treatment, dyslipidemia, resistance to insulin, and nonalcoholic steatosis. However, few studies evaluate the diet effects in rats behavior or cicatrization. The objective of this work was to analyze the influence of the ketogenic diet on the weight gain, emotional behavior of the rats submitted to experimental models such as elevated plus maze (EPM) and open field (OF). The cicatrization time and leukocyte differentiations were also observed. Twenty male Wistar rats of two months age were divided into two groups. One was submitted to ketogenic diet (KD), and the control group (Co) was fed on commercial rations. After 7 days, the animals were weighed and submitted to EPM and OF. A small surgical incision was made and their blood was collected to a leukocyte count. It was verified that the rats from the KD presented less weight gain as compared with the rats from the Co (p < 0.05). The KD did not reveal differences on the behavior measures in the EPM model, but in the OF presented an ambulatory activity significantly bigger. The animals from the KD presented a cicatrization significantly better than Co after 72 h (p = 0.0035) and 96 h (p < 0.1). There was no difference between the groups for leukocyte count. Our results suggest that the KD can interfere on rats deambulation in animal models and improve the cicatrization response.


Subject(s)
Behavior, Animal/drug effects , Cicatrix/diet therapy , Diet, Ketogenic , Motor Activity/drug effects , Weight Gain/drug effects , Animals , Cell Differentiation/drug effects , Exploratory Behavior/drug effects , Leukocyte Count , Leukocytes/drug effects , Male , Maze Learning/drug effects , Models, Animal , Rats , Rats, Wistar
6.
Biometals ; 25(5): 859-62, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22836828

ABSTRACT

Titanium is known to possess excellent biocompatibility as a result of corrosion resistance, lack of allergenicity when compared with many other metals. Fluoride is well known as a specific and effective caries prophylactic agent and its systemic application has been recommended widely over recent decades. Nevertheless, high fluoride concentrations impair the corrosion resistance of titanium. The purpose of this article is to summarize the current data regarding the influence of fluoride on titanium corrosion process in the last 5 years. These data demonstrate noxious effects induced by high fluoride concentration as well as low pH in the oral cavity. Therefore, such conditions should be considered when prophylactic actions are administrated in patients containing titanium implants or other dental devices.


Subject(s)
Fluorides/adverse effects , Mouth/drug effects , Titanium/chemistry , Cariostatic Agents/adverse effects , Chemical Phenomena , Corrosion , Dental Implants , Humans , In Vitro Techniques
7.
Säo Paulo; s.n; 2000. 131 p. ilus.
Thesis in Portuguese | LILACS | ID: lil-272663

ABSTRACT

O labirinto em cruz elevado, apesar de ser um dos modelos experimentais mais usados para o estudo da ansiedade, apresenta uma série de problemas que afetam sua utilização, entre eles, a falta de efeito ansiolítico de drogas serotonérgicas usadas com sucesso na clínica. Uma possível explicação estaria no fato que as drogas testadas no modelo são administradas a uma população normal de animais, enquanto na clínica o efeito é observado em pacientes com quadros patológicos de ansiedade. Assim, o objetivo do presente estudo foi promover uma seleção de ratos ansiosos e não ansiosos no labirinto em cruz elevado e verificar se essas populações selecionadas apresentavam características comportamentais e neuroquímicas diferentes que pudessem caracteriza-las como populações distintas. Foram selecionadas 2 populações de ratos, conforme o tempo de permanência dos mesmos nos braços abertos do labirinto: ansiosos e não ansiosos. Os resultados obtidos mostram que os animais ansiosos apresentaram significantemente menores índices de atividade motora do que os não ansiosos, tanto no modelo do labirinto em cruz elevado (medida pelo número total de entrada, e pelo número de entradas nos braços fechados) quanto no campo aberto (ambulação total e periférica e número de rearings). Em relação as medidas de emocionalidade, os ratos ansiosos mostraram maiores medidas de ansiedade, em relação aos ratos não ansiosos, também no campo aberto (avaliado pela ambulação periférica e tempo de freezing) e no teste de interação social. Também foi medida a concentração de 5-HT e 5-HIAA e tumover ([5-HT/5-HIAA]) no hipocampo e córtex pré frontal dos ratos ansiosos e não ansiosos e foi verificada uma diferença estatística no tumover do córtex pré frontal dos ratos ansiosos, o que sugere uma síntese aumentada de 5-HT no córtex pré frontal dos mesmos. Por fim, se verificou que o triptofano, na dose de 200 mg/kg, mostra efeito ansiolítico no labirinto em cruz elevado. Os resultados indicam uma participação do sistema serotonérgico na modulação da ansiedade. De um modo geral, os dados sugerem que a seleção de animais ansiosos e não ansiosos, pode ser uma importante ferramenta para o estudo da ansiedade


Subject(s)
Anxiety , Ear, Inner , Rats , Serotonin
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