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1.
Bratisl Lek Listy ; 122(10): 715-720, 2021.
Artigo em Inglês | MEDLINE | ID: mdl-34570572

RESUMO

AIMS: The study aim was to analyse the frequency of polymorphic variants of angiotensinogen gene polymorphism (AGT 704T>C, rs699) in essential arterial hypertension (EAH) patients. METHODS: Seventy-two individuals with EAH and hypertension­mediated organ damage (stage 2), moderate, high or very high cardiovascular risks were involved in the case-control study. Among them, 70.84 % (51) were females and 29.16 % (21) were males; mean age was 59.87±7.98 y. The control group consisted of fifty practically healthy individuals at relevant age (49.13±6.28 y) and with relevant sex distribution (62 % were females, 38 % were males). AGT (704T>C) gene polymorphism was examined by RT-PCR. RESULTS: The distribution of genotypes in the study group was as follows: TT - 14 %, TC - 60 %, CC - 26 %, which corresponded to the distribution in the control group - 16 %, 54 % and 30 %, respectively, and did not deviate from the Hardy-Weinberg equilibrium. Smoking, type 2 diabetes mellitus (DM2) and obesity increased the relative risk of EAH in the examined population 2.5 times [OR=2.81; p=0.049], 3.75 times [OR=4.68; p=0.005] and almost twofold [OR=2.90; p=0.004], respectively. The probability of EAH increases fourfold with the angiotensin II elevation in the serum. Genotypes and alleles of the AGT (704T>C) gene were not significant risk factors for EAH and DM2 in the studied population. However, the TC-genotype (lesser T-allele) increases the risk of obesity in EAH patients more than 1.5 times [OR=2.93; p=0.03]. In addition, the T-allele increases the risk for blood pressure (BP) to elevate up to grade 2-3 [OR=3.64; p < 0.001]. CONCLUSIONS: One-way ANOVA analysis confirmed the AGT (704T>C) gene polymorphism to be associated with systolic and diastolic BP elevation (F=7.80; p < 0.001 and F=4.90; p=0.01, respectively), especially in TT-genotype carriers (p < 0.05), and with body mass index increase, albeit only in women (F=13.94; p < 0.001) (Tab. 4, Fig. 3, Ref. 26). Text in PDF www.elis.sk Keywords: angiotensinogen gene (AGT 704T>C), diabetes mellitus type 2, arterial hypertension, obesity, risk.


Assuntos
Diabetes Mellitus Tipo 2 , Hipertensão , Idoso , Angiotensinogênio/genética , Pressão Sanguínea , Estudos de Casos e Controles , Feminino , Frequência do Gene , Genótipo , Humanos , Hipertensão/epidemiologia , Hipertensão/genética , Masculino , Pessoa de Meia-Idade , Obesidade/epidemiologia , Obesidade/genética , Polimorfismo Genético
2.
Mikrobiol Z ; 76(2): 47-53, 2014.
Artigo em Ucraniano | MEDLINE | ID: mdl-25000730

RESUMO

Possible influence of man-made load on formation and function of microbiocenosis of the nose mucosa in practically healthy people of industrial city has been studied. Microbiota composition, content of secretory immunoglobulin A, functional state and expression of TLR-2 and TLR-4 by mucosa cells were studied in the given human biotope. The residing in conventionally contaminated districts of the industrial city tells on the increase of ecologic role of Candida albicans in the composition of microbiocenosis of the nose mucosa. The authors have shown high sensitivity of the number of TLR-4-positive epithelial cells to the type of the basic taxon of a microorganism in the composition of the nose mucosa microbiota and also sensitivity of the number of TLR-2 and TLR-4-positive epithelial cells and the density of expression by TLR-4 epithelial cells to the man-made pollution, they have also established the expressed unbalance of the system of inherent immunity of the nose mucosa of practically healthy young persons in conditions of man-made pollution.


Assuntos
Portador Sadio , Poluição Ambiental , Células Epiteliais/imunologia , Granulócitos/imunologia , Imunidade Inata , Mucosa Nasal/imunologia , Adolescente , Candida albicans/crescimento & desenvolvimento , Portador Sadio/imunologia , Portador Sadio/microbiologia , Células Epiteliais/microbiologia , Expressão Gênica , Granulócitos/microbiologia , Interações Hospedeiro-Patógeno/imunologia , Humanos , Imunoglobulina A/metabolismo , Masculino , Microbiota/imunologia , Mucosa Nasal/microbiologia , Staphylococcus/crescimento & desenvolvimento , Streptococcus/crescimento & desenvolvimento , Receptor 2 Toll-Like/genética , Receptor 2 Toll-Like/imunologia , Receptor 4 Toll-Like/genética , Receptor 4 Toll-Like/imunologia , Ucrânia , População Urbana , Adulto Jovem
3.
Fiziol Zh (1994) ; 54(3): 28-35, 2008.
Artigo em Ucraniano | MEDLINE | ID: mdl-18763577

RESUMO

We investigated the influence of multiple introductions of NO precursor L-arginine and NOS non-selective blocker N-nitroL-arginine (NNLA) on thymic morpho-functional status in Wistar male rats with experimental diabetes mellitus (EDM). To reveal insulin-expressing, proliferating, Treg-cells, iNOS(+)-cells and Bcl-2(+)-cells, the immunohistochemical methods of direct and indirect immunofluorescence with monoclonal antibodies to insulin, PCNA, CD-25 antigen. Bcl-2 and iNOS of rat were used. It was established that NNLA administration to rats with EDM has more pronounced effect in comparison with L-arginine administration, demonstrating an increase in the number of Treg-cells, insulin-expressing and proliferating thymocytes and a decrease in the density of iNOS(+)- and Bcl-2(+)-cells population.


Assuntos
Diabetes Mellitus Experimental , Óxido Nítrico/metabolismo , Timo/efeitos dos fármacos , Animais , Apoptose/efeitos dos fármacos , Arginina/farmacologia , Proliferação de Células/efeitos dos fármacos , Diabetes Mellitus Experimental/imunologia , Diabetes Mellitus Experimental/metabolismo , Diabetes Mellitus Experimental/patologia , Diabetes Mellitus Experimental/fisiopatologia , Inibidores Enzimáticos/farmacologia , Insulina/biossíntese , Masculino , Óxido Nítrico Sintase Tipo II/antagonistas & inibidores , Nitroarginina/farmacologia , Proteínas Proto-Oncogênicas c-bcl-2/metabolismo , Ratos , Ratos Wistar , Linfócitos T/citologia , Linfócitos T/efeitos dos fármacos , Linfócitos T/metabolismo , Timo/imunologia , Timo/metabolismo , Timo/patologia , Timo/fisiopatologia
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