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1.
Cytokine ; 56(2): 312-7, 2011 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-21802960

RESUMO

Sickle cell anemia (SCA) is a disorder characterized by a heterogeneous clinical outcome. In the present study, we investigated the associations between Tumor Necrosis Factor-alpha (TNF-alpha) -308G>A and Interleukin 8 (IL-8) -251A>T gene polymorphisms, medical history and classical biomarkers in children with steady-state SCA. In total, 210 SCA patients aged 2-21 years and 200 healthy controls were studied. Gene polymorphisms, betaS-globin haplotypes and a 3.7-kb deletion in alpha2-thalassemia (α2-thal3.7 kb) were investigated by PCR/RFLP analysis, and cytokine levels were determined by ELISA. Splenomegaly (p=.032) was more prevalent among children younger than 5 years of age. The A allele of the TNF-alpha -308G>A gene polymorphism and the presence of α2-thal3.7 kb were associated with an increase risk of splenic sequestration events (p=.001; p=.046), while the T allele of the IL-8 -251A>T gene polymorphism was considered to be a protective factor for splenomegaly events (p=.032). Moreover, the A allele of the TNF-alpha -308G>A gene polymorphism was associated with high TNF-alpha levels (p=.021), and the hemoglobin F and hemoglobin S haplotypes were correlated with serum levels of IL-8. The logistic regression analysis showed significant effects of the TNF-alpha and IL-8 gene polymorphisms, beta(S)-globin gene haplotypes and α2-thal3.7 kb on the occurrence of splenic sequestration events. Our study emphasizes that the identification of new genetic and immunological biomarkers and their associations with classical markers is an important strategy to elucidate the underlying causes of different SCA phenotypes and their effects on patient outcome.


Assuntos
Anemia Falciforme/sangue , Biomarcadores/sangue , Interleucina-8/sangue , Anamnese , Polimorfismo Genético , Fator de Necrose Tumoral alfa/sangue , Adolescente , Adulto , Alelos , Anemia Falciforme/genética , Estudos de Casos e Controles , Criança , Pré-Escolar , Estudos Transversais , Ensaio de Imunoadsorção Enzimática , Haplótipos , Humanos , Interleucina-8/genética , Reação em Cadeia da Polimerase , Polimorfismo de Fragmento de Restrição , Fator de Necrose Tumoral alfa/genética
2.
Arq. bras. med. vet. zootec. (Online) ; 69(3): 529-534, jun. 2017. tab
Artigo em Inglês | LILACS, VETINDEX | ID: biblio-846838

RESUMO

The success of transvaginal follicular aspiration in mares can be influenced by several factors, such as vacuum pump pressure levels. The present study aimed to investigate the effect of different negative pressures (150, 280 and 400mmHg) of the vacuum pump on the oocyte recovery in the mares. The mares (n=10) were undergoing follicular aspiration using three different negative pressures for three consecutive estrous cycles as follows: G150 = 150mmHg (n = 10); G280 = 280mmHg (n = 10); G400 = 400mmHg (n = 10). Every estrous cycle, the group that the mare would participate was drawn, and each animal participated once in each group. Only preovulatory follicle was used, about 30 to 36 hours after application of hCG. To compare the results, the chi-square test was used (5% significance) and Fisher exact test, when recommended. Thirty preovulatory follicles (diameter 36.1±1.80mm) were aspirated and ten oocytes were recovered (33.3%). There was no statistical difference between the experimental groups (p=0.59). Thus, accord to the results observed in this study, we could conclude that the negative pressure of the vacuum pump used was not efficient to increase oocyte recovery.(AU)


O sucesso da técnica de aspiração folicular transvaginal em éguas pode ser influenciado de maneira determinante por diversos fatores, tais como níveis de pressão da bomba de vácuo. Diante disso, o presente experimento visou investigar o efeito de diferentes pressões negativas (150, 280 e 400mmHg) da bomba de vácuo sobre a taxa de recuperação de oócitos em éguas. As éguas (n=10) foram submetidas à aspiração folicular utilizando-se três diferentes pressões negativas por três ciclos estrais consecutivos, da seguinte maneira: G150= 150mmHg (n=10); G280= 280mmHg (n=10); G400= 400mmHg (n=10). A cada ciclo estral, sorteava-se o grupo do qual a égua participaria, sendo que cada animal integrou um grupo somente uma vez. Foi puncionado somente folículo pré-ovulatório, em torno de 30 a 36 horas após a aplicação do hCG. Os resultados foram comparados utilizando-se o teste qui-quadrado (a 5% de significância) e o Fisher Exato, quando recomendados. Foram aspirados 30 folículos pré-ovulatórios (diâmetro 36,1±1,80mm) e recuperados 10 oócitos (33,3%). Não houve diferença estatística entre os grupos experimentais (P=0,59). Dessa forma, mediante os resultados obtidos no presente estudo, foi possível concluir que a pressão negativa da bomba de vácuo utilizada não se mostrou determinante para elevar a recuperação oocitária.(AU)


Assuntos
Animais , Feminino , Gonadotropina Coriônica , Cavalos , Recuperação de Oócitos/métodos , Folículo Ovariano , Infertilidade Feminina
3.
Braz J Med Biol Res ; 43(8): 705-11, 2010 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-20602015

RESUMO

Fetal hemoglobin (HbF), encoded by the HBG2 and HBG1 genes, is the best-known genetic modulator of sickle cell anemia, varying dramatically in concentration in the blood of these patients. This variation is partially associated with polymorphisms located in the promoter region of the HBG2 and HBG1 genes. In order to explore known and unknown polymorphisms in these genes, the sequences of their promoter regions were screened in sickle cell anemia patients and correlated with both their HbF levels and their betaS-globin haplotypes. Additionally, the sequences were compared with genes from 2 healthy groups, a reference one (N = 104) and an Afro-descendant one (N = 98), to identify polymorphisms linked to the ethnic background.The reference group was composed by healthy individuals from the general population. Four polymorphisms were identified in the promoter region of HBG2 and 8 in the promoter region of HBG1 among the studied groups. Four novel single nucleotide polymorphisms (SNP) located at positions -324, -317, -309 and -307 were identified in the reference group. A deletion located between -396 and -391 in the HBG2 promoter region and the SNP -271 C-->T in the HBG1 promoter region were associated with the Central African Republic betaS-globin haplotype. In contrast, the -369 C-->G and 309 A-->G SNPs in the HBG2 promoter region were correlated to the Benin haplotype. The polymorphisms -396_-391 del HBG2, -369 SNP HBG2 and -271 SNP HBG1 correlated with HbF levels. Hence, we suggest an important role of HBG2 and HBG1 gene polymorphisms on the HbF synthesis.


Assuntos
Anemia Falciforme/genética , Polimorfismo Genético/genética , Regiões Promotoras Genéticas/genética , gama-Globinas/genética , Idoso , Anemia Falciforme/sangue , População Negra , Brasil , Criança , Feminino , Genótipo , Haplótipos , Humanos , Masculino
4.
Rev. bras. pesqui. méd. biol ; Braz. j. med. biol. res;43(8): 705-711, Aug. 2010. tab
Artigo em Inglês | LILACS | ID: lil-554960

RESUMO

Fetal hemoglobin (HbF), encoded by the HBG2 and HBG1 genes, is the best-known genetic modulator of sickle cell anemia, varying dramatically in concentration in the blood of these patients. This variation is partially associated with polymorphisms located in the promoter region of the HBG2 and HBG1 genes. In order to explore known and unknown polymorphisms in these genes, the sequences of their promoter regions were screened in sickle cell anemia patients and correlated with both their HbF levels and their ƒÀS-globin haplotypes. Additionally, the sequences were compared with genes from 2 healthy groups, a reference one (N = 104) and an Afro-descendant one (N = 98), to identify polymorphisms linked to the ethnic background.The reference group was composed by healthy individuals from the general population. Four polymorphisms were identified in the promoter region of HBG2 and 8 in the promoter region of HBG1 among the studied groups. Four novel single nucleotide polymorphisms (SNP) located at positions -324, -317, -309 and -307 were identified in the reference group. A deletion located between -396 and -391 in the HBG2 promoter region and the SNP -271 C¨T in the HBG1 promoter region were associated with the Central African Republic ƒÀS-globin haplotype. In contrast, the -369 C¨G and 309 A¨G SNPs in the HBG2 promoter region were correlated to the Benin haplotype. The polymorphisms -396_-391 del HBG2, -369 SNP HBG2 and -271 SNP HBG1 correlated with HbF levels. Hence, we suggest an important role of HBG2 and HBG1 gene polymorphisms on the HbF synthesis.


Assuntos
Idoso , Criança , Feminino , Humanos , Masculino , Anemia Falciforme/genética , Polimorfismo Genético/genética , Regiões Promotoras Genéticas/genética , gama-Globinas/genética , População Negra , Anemia Falciforme/sangue , Brasil , Genótipo , Haplótipos
5.
Rev. bras. ciênc. mov ; 14(3): 105-112, 2006.
Artigo em Português | LILACS | ID: lil-524626

RESUMO

A região lombar desempenha um papel fundamental na acomodação de cargas decorrentes do peso corporal, da ação muscular e das forças aplicadas externamente. A funcionalidade dessa região é mantida através do sinergismo entre os mecanismos ativo, passivo e neural da estabilização lombar. O desequilíbrio proporcionará a instabilidade que terá como principal conseqüência à dor. O objetivo do estudo foi mostrar a íntima relação existente entre a Fáscia Tóraco Lombar e mecanismo ativo de estabilização lombar. A metodologia utilizada foi baseada na revisão bibliografia de estudos realizados no período de 1984 a 2004, sendo 43 artigos científicos e 10 livros. Destes, foram utilizados no trabalho, 20 artigos e 8 livros. Os bancos de dados pesquisados foram Lilás, Medline e Pedro. O estudo pôde confirmar que a Fáscia Tóraco Lombar é uma estrutura passiva que apresenta conecção com diversos músculos, comporta a função de suporte mecânico e participa dinamicamente, complementando a ação das outras estruturas estabilizadoras. Logo, a reabilitação de pacientes lombálgicos deve se basear em atividades que aprimorem a função de cada um dos componentes deste complexo mecanismo de estabilização.


The lumbar region has a major role concerning load accommodation due to body weight, muscle action and externally applied forces. The workability of this region is kept through the synergism among lumbar stabilization active, passive and neural mechanisms. Unbalance will result in instability, and pain will be its main consequence. This study aims to show the close relation between thoracolumbar fascia and the active system of lumbar stabilization. The applied methodology was based on the bibliographical review of 43 scientific articles and 10 books published between 1984 and 2004. From this whole, 8 books and 20 articles have been used in this work. The data research were Lilás, Medline and Pedro. The describers were thoracolumbar fascia, stabilization and active system. This study show that thoracolumbar fascia is a passive structure which is connected to several muscles, thus providing mechanical support, as well as dynamic cooperation to complement the action of other stabilizing structures. Lumbago patients’ rehabilitation must be based on activities which improve the function of each component in this complex stabilizing mechanism.


Assuntos
Humanos , Exercício Físico , Fáscia , Região Lombossacral
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