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1.
Dental press j. orthod. (Impr.) ; 23(5): 41-46, Sept.-Oct. 2018. tab, graf
Article in English | LILACS | ID: biblio-975013

ABSTRACT

ABSTRACT Introduction: The search for more aesthetic and comfortable orthodontic devices has led to an increase in the use of clear aligners. Objective: To increase knowledge on biological mechanisms of orthodontic tooth movement using Invisalign aligners. Methods: This study included 11 patients with a mean age of 23.6 ± 4.8 years. Cases planning included alignment and leveling of lower incisors using Invisalign aligners. Gingival crevicular fluid samples were collected from the lower incisors on the day of delivery of aligner number 1 (T0) and after 1 (T24h), 7 (T7d), and 21 (T21d) days. During the observation period of the study, the patients used only the aligner number 1. Levels of nine cytokines were quantified using Luminex's multi-analysis technology. Non-parametric tests were used for comparisons between cytokine expression levels over time. Results: Cytokine expression levels remained constant after 21 days of orthodontic activation, except those of MIP-1β, which presented a statistical difference between T24h and T21d with a decrease in the concentration levels. IL-8, GM-CSF, IL-1β, MIP-1β, and TNF-α showed the highest concentrations over time. Conclusions: The different behavior in the levels of the investigated cytokines indicates a role of these biomarkers in the tissue remodeling induced by Invisalign.


RESUMO Introdução: a busca por dispositivos ortodônticos mais estéticos e confortáveis gerou um aumento no uso de alinhadores transparentes. Objetivo: ampliar o conhecimento sobre os mecanismos biológicos associados ao movimento dentário ortodôntico promovido por alinhadores Invisalign®. Métodos: a amostra foi constituída por 11 pacientes, com idade média de 23,6 ± 4,8 anos. O planejamento dos casos incluiu alinhamento e nivelamento de incisivos inferiores usando os alinhadores. O fluido gengival crevicular foi coletado na superfície vestibular de incisivos inferiores no dia da entrega do alinhador número 1 (T0) e após 1 (T24h), 7 (T7d) e 21 (T21d) dias. Durante o período de observação do estudo, os pacientes utilizaram apenas o alinhador número 1. Os níveis de nove citocinas foram quantificados por meio do sistema Luminex de multianálise. Testes não paramétricos foram realizados para comparações entre os níveis de expressão de citocinas ao longo do tempo. Resultados: a concentração das citocinas manteve-se constante após 21 dias de ativação ortodôntica, exceto a MIP-1β, que apresentou uma redução estatisticamente significativa entre os tempos T24h e T21d. As IL-8, GM-CSF, IL-1β, MIP-1β e TNF-α apresentaram as maiores concentrações ao longo do tempo. Conclusão: a constância na expressão dos níveis das citocinas parece estar compatível com o estímulo mecânico induzido por alinhadores.


Subject(s)
Humans , Male , Female , Young Adult , Tooth Movement Techniques , Cytokines/analysis , Gingival Crevicular Fluid/chemistry , Orthodontic Appliances, Removable , Cytokines/metabolism , Granulocyte-Macrophage Colony-Stimulating Factor/analysis , Interleukin-8/analysis , Colony-Stimulating Factors/analysis , Interleukin-7/analysis , Tumor Necrosis Factor-alpha/analysis , Chemokine CCL2/analysis , Interleukin-17/analysis , Interleukin-1beta/analysis , Chemokine CCL4/analysis , Incisor
2.
Braz. j. pharm. sci ; 52(3): 375-382, July-Sept. 2016. tab, graf
Article in English | LILACS | ID: biblio-828262

ABSTRACT

ABSTRACT It is well established that protein malnutrition (PM) impairs immune defenses and increases susceptibility to infection. Macrophages are cells that play a central role in innate immunity, constituting one of the first barriers against infections. Macrophages produce several soluble factors, including cytokines and growth factors, important to the immune response. Among those growth factors, granulocyte-macrophage colony-stimulating factor (GM-CSF) and macrophage colony-stimulating factor (M-CSF). GM-CSF and M-CSF are important to monocyte and macrophage development and stimulation of the immune response process. Knowing the importance of GM-CSF and M-CSF, we sought to investigate the influence of PM on macrophage production of these growth factors. Two-month-old male BALB/c mice were subjected to PM with a low-protein diet (2%) and compared to a control diet (12%) mouse group. Nutritional status, hemogram and the number of peritoneal cells were evaluated. Additionally, peritoneal macrophages were cultured and the production of GM-CSF and M-CSF and mRNA expression were evaluated. To determine if PM altered macrophage production of GM-CSF and M-CSF, they were stimulated with TNF-α. The PM animals had anemia, leukopenia and a reduced number of peritoneal cells. The production of M-CSF was not different between groups; however, cells from PM animals, stimulated with or without TNF-α, presented reduced capability to produce GM-CSF. These data imply that PM interferes with the production of GM-CSF, and consequently would affect the production and maturation of hematopoietic cells and the immune response.


Subject(s)
Rats , Granulocyte-Macrophage Colony-Stimulating Factor/analysis , Macrophage Colony-Stimulating Factor/analysis
3.
Arq. neuropsiquiatr ; 50(2): 180-2, jun. 1992. tab
Article in English | LILACS | ID: lil-120728

ABSTRACT

Detectamos as citocinas interleucina-6 (IL-6) e granulócito-macrófago-CSF (GM-CSF) por ELISA no LCR e soro de 30 pacientes infectados por HIV classificados como tendo AIDS-demência complexo (ACD) e de 20 pacientes com outras doenças neurológicas (OND). Encontramos elevada incidência de IL-C e GM-CSF detectável no LCR de pacientes com ADC, em relaçäo aos pacientes com OND. Diferenças estatísticas näo foram observadas entre os dois grupos de pacientes para níveis de IL-6 e GM-CSF no soro. Esses resultados sugerem síntese intratectal dessas citocinas e sua possível participaçäo na patogenia da ADC


Subject(s)
Humans , Male , Female , Adult , AIDS Dementia Complex/cerebrospinal fluid , Granulocyte-Macrophage Colony-Stimulating Factor/analysis , Interleukin-6/analysis , AIDS Dementia Complex/blood , Central Nervous System Diseases/cerebrospinal fluid , Central Nervous System Diseases/blood , Enzyme-Linked Immunosorbent Assay
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