Introdução: O sobrepeso e a obesidade representam um grave problema de Saúde Pública, tendo seu desenvolvimento associado à adolescência, impacto negativo na fase adulta, sobretudo, devido suas complicações metabólicas. Considerando que o caráter crônico e inflamatório de baixa intensidade presente na obesidade estimula a geração de radicais livres, torna-se relevante avaliar a relação entre as adipocitocinas e a oxidação das lipoproteínas. Objetivos: Avaliar a possível influência da obesidade sobre a LDL(-) e adipocitocinas. Material e Métodos: Foram recrutados 156 adolescentes de ambos os sexos, com faixa etária de 10 a 19 anos e regularmente matriculados em escolas públicas da cidade de São Paulo. Os adolescentes foram distribuídos em três grupos: Eutrófico, Sobrepeso e Obeso, segundo COLE et al. (2000). Após jejum (12-15h) foi coletada uma amostra de sangue e a partir do plasma realizamos as seguintes análises: perfil lipídico, glicose e insulina (kits comerciais), LDL(-) e seus auto-anticorpos (ELISA), leptina, resistina e adiponectina (ELISA). O perfil sócio-econômico e clínico dos adolescentes foi investigado por meio de questionários estruturados. Foram coletadas informações antropométricas (peso, altura, circunferência da cintura, porcentagem de gordura) e dados de consumo alimentar (3 x R24h). O consumo alimentar foi estimado por meio do programa NutWin®. As diferenças entre as variáveis qualitativas foram determinadas pelo teste c2. As variáveis quantitativas foram ajustadas pela idade por meio do General Linear Model, sendo as diferenças entre os grupos estabelecidas pelo teste post-hoc de Bonferroni (SPSS®, versão 15.0). Resultados: Dos 156 adolescentes incluídos no estudo, 76 (48,7 por cento ) foram meninos e 80 (51,3 por cento ) meninas, com idade média de 14,5 ± 2,3 anos. Os adolescentes foram distribuídos em três grupos: Eutrófico (n = 52 adolescentes; 33,3 por cento ), Sobrepeso (n = 53 adolescentes; 34,0 por cento ) e Obeso (n = 51 adolescentes; 32,7 por cento ). Estes grupos foram pareados quanto ao sexo, escolaridade da mãe, renda, maturação sexual e antecedentes familiares de doenças. Como previsto pelo critério de estratificação dos grupos, os valores médios de IMC foram diferentes entre os grupos, sendo confirmados pela CC e porcentagem de gordura. Em relação ao hábito alimentar, a análise dos dados brutos e ajustados pela energia e variabilidade intrapessoal não apresentou diferença entre 4 os grupos. As análises da glicemia de jejum, colesterol total, triacilgliceróis e LDL-C não apresentaram diferenças entre os grupos. A insulina plasmática no grupo Obeso apresentou valores superiores aos grupos Eutrófico (p< 0,001) e Sobrepeso (p< 0,001), e o índice HOMA-IR no grupo Obeso apresentou valores superiores aos grupos Eutrófico (p< 0,001) e Sobrepeso (p< 0,001), enquanto o HDL-C apresentou valores maiores no grupo Eutrófico, quando comparado ao Obeso (p=0,012). A LDL(-) e seus autoanticorpos apresentaram diferentes concentrações entre os grupos (p= 0,040; p= 0,026, respectivamente). A leptina no grupo Eutrófico apresentou valores menores que os grupos Sobrepeso (p< 0,001) e Obeso (p< 0,001), assim como o grupo Sobrepeso apresentou valores inferiores ao grupo Obeso (p< 0,001). Perfil inverso foi observado em relação à concentração de adiponectina, A resistina apresentou valores maiores no grupo Obeso (p= 0,006), que no grupo Eutrófico. A leptina apresentou correlações positivas com percentual de gordura (r= 0,540; p= 0,001), circunferência da cintura (r= 0,679; p= 0,003) e IMC (r= 0,670; p< 0,001). Em relação ao metabolismo de carboidratos, a leptina se correlacionou positivamente com a insulina (r= 0,578; p< 0,001) e o HOMA-IR (r= 0,570; p= 0,001), enquanto a adiponectina se correlacionou negativamente com insulina (r= -0,255; p= 0,001) e o HOMA-IR (r= -0,246; p=0,002). Em relação ao perfil lipídico, a leptina correlacionou-se com colesterol total (r= 0,496; p= 0,003), triacilgliceróis (r= 0,409; p= 0,016) e LDL-C (r= 0,416; p= 0,014), assim como a adiponectina correlacionou-se com LDL(-) (r= -0,428; p= 0,012) e a resistina com HDL-C (r= -0,337; p= 0,050). Portanto, os resultados obtidos demonstram que adolescentes com excesso de peso, mesmo ainda considerados clinicamente saudáveis, apresentam diversos parâmetros antropométricos e bioquímicos alterados, que sugerem a presença de um elevado número de fatores de risco cardiometabólico nessa população / Introduction: Overweight and obesity represent a serious Public Health issue. Their development associated with adolescence, generate a negative impact in adulthood, mainly because of metabolic complications. As the low and chronic inflammatory state present in obesity stimulates the generation of free radicals, it becomes relevant to assess the relationship between adipocytokines and the oxidation of lipoproteins. Objective: Evaluate the possible influence of overweight and obesity on the electronegative LDL and adipocytokines (leptin, adiponectin and resistin). Materials and Methods: Adolescents of both genders, aged 10 to 19 years old and regularly registered in public schools at the city of São Paulo were recruited for this research. They were divided into three groups: Healthy weight, Overweight and Obese, according to Cole et al. (2000), by gender and age. After fasting (12-15h) a blood sample was collected and the following tests were performed on each samples plasma: total lipid profile, glucose and insulin (commercial kits), leptin, resistin, adiponectin (ELISA), LDL(-) (ELISA) and its autoantibodies (ELISA). The socio-economic and health profiles of the adolescents were determined by structured questionnaires. Anthropometric (weight, height, waist circumference - WC, percentage of body fat) and food consumption data (3 x 24-hour recall) were collected. The 24-hour recall data was analyzed by the NutWin® software. Differences between qualitative variables were determined by c2 test. Quantitative variables were adjusted for age by means of General Linear Model, being the differences between the groups established by post-hoc Bonferroni test (SPSS ®, version 15.0). Results: Of the 156 eligible individuals, 76 (48.7 per cent ) were boys and 80 (51.3 per cent ) girls, with the average age being of 14.5 ± 2.3 years. The adolescents were divided into three groups: Healthy weight, n = 52 adolescents (33.3 per cent ), Overweight, n = 53 adolescents (34.0 per cent ) and Obese, n = 51 adolescents (32.7 per cent ). These groups were matched up by gender, mother\'s education, income, sexual maturation, and current medical history. As expected by the group inclusion criteria, there were statistical differences in BMI and this profile was confirmed by WC and body fat. Opposite profile was showed for lean body mass. In relation to food consumption, the analysis of crude data adjusted for energy and intrapersonal variability did 6 not differ between the groups. Analyses of fasting glucose, total cholesterol, triglycerides and LDL-C did not differ between the groups. There were higher levels of plasma insulin and HOMA-IR in the obese group than in the healthy weight (p <0.001; p <0.001) and the overweight (p <0.001; p < 0.001) groups. HDL-C in the healthy weight group showed increased values in comparison to Obese one (p = 0.012). The LDL (-) in plasma and its autoantibodies indicated different concentrations between the groups (p = 0.040, p= 0.026, respectively). There were lower values of leptin both in the healthy weight group in comparison with the overweight (p <0.001) and the obese (p <0.001) groups, as well as in the Overweight group in comparison with the Obese group (p <0.001). Opposite profile was observed for adiponectin levels, between the healthy weight group and the overweight (p = 0.019) and obese (p = 0.000) groups. Resistin showed higher values in the obese group (p = 0.006) than in the healthy weight group. Leptin showed positive correlations with body fat percentage (r= 0.540 and p= 0.001), waist circumference (r= 0.679 and p= 0.003) and BMI (r= 0.670 and p <0.001). In relation to carbohydrate metabolism, leptin correlated positively with insulin (r= 0.578 and p <0.001) and HOMA-IR (r= 0.570 and p= 0.001), and opposite profile was showed for adiponectin (Insulin: r= -0.255, p= 0.001; HOMA-IR: r= -0.246, p= 0.002, respectively). Regarding the lipid profile, leptin correlated with total cholesterol (r= 0.496 and p= 0.003), triglycerides (r= 0.409 and p= 0.016) and LDL-C (r= 0.416 and p= 0.014); adiponectin correlated with LDL (-) (r= -0.428, p= 0.012); and resistin with HDL-C (r= -0.337, p= 0.050). Therefore, the results show that overweight and obese adolescents, even those who are still considered clinically healthy, showed several anthropometric and biochemical changes, which suggest increased number of cardiometabolic risk factors in this population

O presente trabalho avaliou os efeitos provocados pela laserterapia de baixa intensidade (LTBI) no \'lâmbda\' 780 nm, 30 mW de potência e tempo de exposição de 150 segundos, resultando em uma fluência de 112,5 J/\'CM POT.2\' e energia total de 4,5 J, sobre o comportamento osteocondutor da vitrocerâmica elaborada a partir do genérico do biovidro de composição: 45% \'SI\'O IND.2\', 24,5% \'NA IND.2\'O\', 24,5% \'CA\'O\' e 6% \'P IND.2\'O IND.5\' em perfurações ósseas em tíbias de ratos. O biovidro foi recozido em cuba de inox acima de sua temperatura de transição vítrea, a 620 graus Celsius por 30 minutos e mantido a 790 graus Celsius por 60 minutos, em seguida foi realizada a espectroscopia Raman para verificar a cristalinidade. Foram realizadas perfurações abaixo da tuberosidade da tíbia direita de 64 machos de ratos da raça Wistar (Rattus norvegicus albinus) na idade adulta. Os mesmos foram divididos aleatoriamente em 4 grupos sendo eles: um controle e três submetidos à procedimento experimental de implante e/ou irradiação laser de baixa intensidade. Em todos os grupos foram utilizados 16 indivíduos. Posteriormente, os animais de cada grupo foram subdivididos em dois subgrupos cada, de acordo com o tempo de vida antes da eutanásia, que ocorreu com 7 e 13 dias P.O. A análise das características das fibras colágenas para determinar a neoformação tecidual, bem como seu estado de maturação, foi realizada através de corpos de prova em forma de lâminas coradas com HE observadas à microscopia de luz comum para verificar a presença de células no foco de lesão, lâminas coradas com Picro Sirius sob luz polarizada a fim de verificar o estado organizacional e microscopia eletrônica de varredura, utilizando métodos técnico-experimentais para avaliar a interação do biomaterial com o tecido ósseo. Os valores de birrefringência demonstraram uma melhor organização tecidual dos grupos irradiados com ou sem o implante de vitrocerâmico (p < 0,05), os grupos com vitrocerâmico apresentaram o tecido mais difuso, até mesmo nas regiões mais centrais da lesão aos 13 dias. O vitrocerâmico estimulou a proliferação osteoblástica (p < 0,05), assim como a radiação laser (p < 0,01). Pode-se concluir que o vitrocerâmico utilizado apresenta capacidade osteocondutora e que a radiação laser acelerou o processo de reparo na presença ou não do vitrocerâmico. / The present study evaluated the effects caused by the low level laser therapy (LLLT) at \'lâmbda\' 780 nm, power of 30 mW and dose of 112.5 J/\'CM POT.2\' and total energy of 4.5 J on the behavior osteoconductor of the glass-ceramic drafted from generic of bioglass of composition: 45% \'SI\'O IND.2\', 24.5% \'NA IND.2\'O\', 24.5% \'CA\'O\' and 6% \'P IND.2\'O IND.5\' in drillings in tibia bone of rats. The bioglass was anneal in cuba of stainless above its glass transition temperature, to 620 Celsius degrees for 30 minutes and maintained at 790 Celsius degrees for 60 minutes, then was held to Raman spectroscopy to verify the crystallinity. Drillings were made below the tuberosity of the right tibia of 64 males of the race Wistar rats (Rattus Norvegicus Albinus) in adult age. They were randomly divided into 4 groups which are: a control and three underwent experimental procedure to implant and/or of low intensity laser irradiation. In all groups were used 16 individuals. Later, the animals in each group were further divided into two subgroups each, according to the time of life before euthanasia, which occurs with 7 and 13 days postoperative. The analysis of the characteristics of collagen fibers was conducted through: slides stained with HE seen the light microscopy, to quantify the presence of cells in the focus of injury, slides stained with Picro Sirius Red under polarized light to verify the organizational state, microscope electronic scanning, using technical experimental methods to evaluate the interaction of biomaterial with the bone tissue. The values of birefringence showed better tissue organization of groups irradiated with or without the implant of glass-ceramic (p < 0.05), the groups with glass-ceramic showed collagen fibers more diffuse, even in the most central of injury to 13 days. The glass-ceramic stimulated the osteoblast proliferation (p < 0.05) as well as laser radiation (p < 0.01). Thus it is possible to conclude that the glass-ceramic has osteoconductive capacity and that laser radiation accelerated the process of repairing in the presence or not of glass-ceramic.

Foi utilizado na presente pesquisa o ultra-som pulsado de baixa intensidade, com a finalidade de avaliar, experimentalmente, seus efeitos físicos sobre a regeneração do músculo esquelético de ratos. Foram empregados no experimento 10 animais de ambos os sexos. Após eleição do músculo glúteo maior, foram feitas incisões perpendiculares (pós anestesia) às suas fibras, alcançando aproximadamente dois terços de sua espessura. Seguinte às incisões, realizou-se síntese do músculo e dos planos superficiais. Foi convencionado estudar os efeitos do ultra-som pulsado após 3, 6 e 10 dias de estímulo. Antes do sacrifício dos animais foi-lhes administrado Colchicina, com a finalidade de bloquear a células em divisão. Mediante análise histopatológica comparativa dos músculos, constatou-se que enquanto nos animais não estimulados desenvolveu-se, aos 3 dias, áreas de necrose e inflamação, naqueles estimulados houve uma diminuição das mesmas. Além disso, nos animais estimulados, ocorre intensa neovascularização nas áreas de lesão. Observou-se também uma migração de células miogênicas (satélites) para restos de bainhas remanescentes de fibras musculares regeneradas. Constatou-se um aumento de mioblastos com núcleos em metáfase. Aos 10 dias, os animais estimulados exibiam inúmeros miotubos com formação de miofibrilas, caracterizando células musculares em franca maturação. Longe da área estimulada, o ultra-som foi capaz de induzir mitoses em células satélites. Notou-se que os efeitos do ultra-som pulsado aceleram a regeneração de fibras musculares mediante uma intensa neoformação vascular, acelerando a reparação da necrose e formação de mioblastos, os quais agregam-se em miotubos formando novas células. / It was used in the present research the low intensity pulsed ultrasound with aim of evaluating, experimentally, its physical effects on the regeneration of rats skeletal muscle. Ten male and female animals were used in this experiment. After election of the gluteus maximus muscle, perpendicular incisions were made (after anesthesia) in its fibers, reaching approximately two thirds of its thickness. After the incisions, a synthesis of the muscles and superficial plans was performed. It was established to study the effects of the pulsed ultrasound after 3, 6 and 10 day-stimuli. Before sacrificing the animals Colchinine was given aiming to block cells in division. By means of comparative histopathological analysis of the muscles, it was verified that in non-stimulated animals an area of necrosis developed in three days, while in those that were simulated there was a decrease of the same. Moreover, on the stimulated animals, there is intense neovascularization in the damaged area. A migration of myogenic cells (satellites) to rests of remaining sheaths from regenerated muscle fiber was also observed. It was verified an increase of myoblasts with nuclei in metaphase. In ten days, the stimulated animals showed countless myotubes with formations of myofibrils, characterizing mature muscle cells. Far from the stimulated area, the ultrasound was able of inducing mitosis to satellite cells. It was noticed that the effects of the pulsed ultrasound accelerate muscle fiber regeneration by means of an intense vascular neoformation, accelerating the restoration of the necrosis and the formation of myoblasts, which aggregates in myotubes forming new cells.

Previous studies have shown growth hormone and therapeutic low intensity pulsed ultrasound can enhance mandibular growth separately. The aim of this study is to evaluate the concomitant effect of both of these applications on mandibular growth in rat. Methods: 24 male Sprague Dawley rats were divided into four groups, 6 in each. Groups 1, 2, 3, and 4 were designated as untreated control, recombinant rat growth hormone, Low Intensity Pulsed Ultrasound, and combination of both groups respectively. After 21 days of daily treatment on mandibular condylar, mandibles from euthanized rats are dissected, and scanned by MicroComputed Tomography to measure the mandibular bone volume, bone surface area, and condylar bone mineral density. Also Real-time Polymerase Chain Reaction was performed on the extracted livers’ C-fos, C-jun, and IGF-1 genes expressions. Results: Groups 2, 3 and 4 showed significant (p<0.05) growth stimulation when compared to the untreated control group. However, there was no statistical significant difference between groups 2, 3 and 4 with regard to bone volume or surface area. Conversely, condylar bone mineral density for group 4 was significantly reduced than groups 1, 2, and 3. Rats’ weights were not significantly different among the treatment groups after the treatment was performed. Additionally, gene expression study showed that the expression of C-jun, in harvested livers for Group 4 was less than that of Group 2 showing fewer side effects. Conclusion: When growth hormone was applied to rats’ mandible together with therapeutic ultrasound, preferential increase in bone volume, and surface area occurred with the expense of condylar bone mineral density and with less potential side effects. / Pharmaceutical Science

Thesis (M.A. in National Security Affairs)--Naval Postgraduate School, June 2003. / Thesis advisor(s): James A. Russell, Gregory K. Mislick. Includes bibliographical references (p. 67-69). Also available online.

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The objective of these experiments is to explore the effect of LIPUS on the ultraexpansion and osteogenic differentiation of harvested passage-4 HUCPV-SCs. HUCPV-SCs were divided into two groups: a treatment group that received LIPUS for 10 minutes for 1, 7, and 14 days and a control group that received a sham treatment utilizing both basic and osteogenic media. The results in basic media and osteogenic media demonstrated nonsignificant differences in cell count, ALP, DNA content, and CD90. Statistically significant expression of OSP and PCNA was observed on day 14 in LIPUS treated group. Nucleostemin expression in the LIPUS-treated group was insignificant on days 1 and 7. However, a selective increase in osteogenic markers was obtained on day 7 for ALP and OCN and on day 14 for OPN. Future experiments are required to explore the effects of different application times and/or techniques of LIPUS on the behaviour of HUCPV-SCs. / Medical Science

Thesis (M.A. in National Security Affairs) Naval Postgraduate School, December 1995. / "December 1995." Thesis advisor(s): Dana P. Eyre, James J. Wirtz. Includes bibliographical references (p. 107-109). Also available online.

Made available in DSpace on 2014-10-09T12:28:25Z (GMT). No. of bitstreams: 0 / Made available in DSpace on 2014-10-09T13:56:26Z (GMT). No. of bitstreams: 0 / Dissertacao (Mestrado Profissionalizante em Lasers em Odontologia) / IPEN/D-MPLO / Instituto de Pesquisas Energeticas e Nucleares - IPEN-CNEN/SP; Faculdade de Odontologia, Universidade de Sao Paulo, Sao Paulo