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2.
J Physiol Pharmacol ; 66(2): 191-202, 2015 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-25903950

RESUMO

Brain-derived neurotrophic factor (BDNF) is involved in the proliferation of neurons, and its expression increases significantly with exercise. We aimed to investigate the effects of chronic exercise (swimming) and sustained hypoxia on cortical BDNF expression in both the presence and absence of vitamin E. Sixty four male Sprague-Dawley rats were divided into two equal groups; a normoxic group and a hypoxic group. Both groups were equally subdivided into four subgroups: sedentary, sedentary with vitamin E, chronic exercise either with or without vitamin E supplementation. Arterial PO(2), and the levels of cortical malondialdehyde (MDA), antioxidants (reduced glutathione GSH, superoxide dismutase (SOD), catalase (CAT) and vitamin E) and BDNF gene expression were investigated. Hypoxia significantly increased MDA production and BDNF gene expression and decreased the antioxidants compared to control rats. Chronic exercise in hypoxic and normoxic rats increased MDA level and BDNF gene expression and decreased the antioxidants. Providing vitamin E supplementation to the hypoxic and normoxic rats significantly reduced MDA and BDNF gene expression and increased antioxidants. We conclude that sustained hypoxia and chronic exercise increased BDNF gene expression and induced oxidative stress. Moreover, vitamin E attenuated the oxidative stress and decreased BDNF gene expression in sustained hypoxia and chronic exercise which confirms the oxidative stress-induced stimulation of BDNF gene expression.


Assuntos
Fator Neurotrófico Derivado do Encéfalo/genética , Córtex Cerebral/efeitos dos fármacos , Expressão Gênica/efeitos dos fármacos , Hipóxia/fisiopatologia , Estresse Oxidativo/efeitos dos fármacos , Condicionamento Físico Animal/fisiologia , Vitamina E/administração & dosagem , Animais , Antioxidantes/metabolismo , Córtex Cerebral/metabolismo , Expressão Gênica/genética , Hipóxia/metabolismo , Masculino , Malondialdeído/metabolismo , Estresse Oxidativo/genética , Ratos , Ratos Sprague-Dawley , Natação/fisiologia
3.
Andrologia ; 47(5): 525-30, 2015 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-24865344

RESUMO

This study aimed to assess cytochrome (CY) P450-2D6*4 polymorphism relationship with semen variables in infertile men. In all, 308 men were included; fertile normozoospermia (N) (n = 77), asthenozoospermia (A) (n = 70), asthenoteratozoospermia (AT) (n = 75) and oligoasthenoteratozoospermia (OAT) (n = 86). They were subjected to history taking, clinical examination, semen analysis, sperm acrosin activity, seminal malondialdehyde (MDA) and CYP450-2D6*4 genotyping. CYP450-2D6*4 wild-type allele was represented in 76.5% of N, 70% of A, 66.7% of AT and 57.7% of OAT men where homozygous gene mutation was present in 5.9% of N, 20% of A, 26.6% of AT and 26.9% of OAT men, respectively. Sperm acrosin activity, sperm concentration, sperm motility, linear sperm velocity and sperm normal forms were significantly higher, and seminal MDA level was significantly lower in men with CYP450-2D6*4 wild-type allele compared with men with homozygous mutation. It is concluded that CYP450-2D6*4 wild-type allele has higher frequency where homozygous-type allele has lower frequency in N men compared with A, AT and OAT men. Sperm acrosin activity index, sperm concentration, sperm motility, linear sperm velocity and sperm normal forms were significantly higher, and seminal MDA level was significantly lower in men with CYP450-2D6*4 wild-type allele compared with men with homozygous mutation.


Assuntos
Citocromo P-450 CYP2D6/genética , Infertilidade Masculina/genética , Motilidade dos Espermatozoides/genética , Acrosina/metabolismo , Adulto , Alelos , Astenozoospermia/genética , Estudos de Casos e Controles , Genótipo , Humanos , Masculino , Malondialdeído/metabolismo , Oligospermia/genética , Polimorfismo Genético , Sêmen/química , Análise do Sêmen , Contagem de Espermatozoides
4.
Genet Mol Res ; 13(3): 8025-34, 2014 Sep 29.
Artigo em Inglês | MEDLINE | ID: mdl-25299117

RESUMO

Hepatocellular carcinoma (HCC) is the fifth most common malignancy worldwide. In Egypt, the incidence of HCC has doubled over the last decade. Matrix metalloproteinase-9 (MMP-9) plays a key role in cancer invasion and metastasis by degrading the extracellular matrix and basement membrane barriers. A cytosine (C)/thymidine (T) single nucleotide polymorphism at position -1562 in the MMP-9 promoter is reported to influence the expression of the MMP-9 gene. The association between MMP-9 gene polymorphisms and HCC patients with hepatitis C and B viruses (HCV and HBV) was examined in 91 patients with HCC and viral hepatitis (55 HCV and 36 HBV). The results were compared with those of 42 HCC patients without viral hepatitis and 60 healthy individuals with no liver infection. Polymorphisms of the MMP-9 gene were investigated by polymerase chain reaction amplification followed by restriction fragment length polymorphism analysis. The serum MMP-9 level was quantitatively determined using a human MMP-9 enzyme-linked immunosorbent assay, which showed that homozygosity of the MMP-9 promoter (TT) was more frequent in patients with HCC and chronic HCV or HBV infection when compared with the control group (49.1, 52.8, and 35.7%, respectively). In addition, we observed significant elevation of serum MMP-9 levels in all HCC groups compared to controls. It was concluded that patients with the MMP-9 TT genotype are at risk of developing HCC and HBV or HCV. People with significantly elevated serum levels of MMP-9 are at risk of developing HCC.


Assuntos
Carcinoma Hepatocelular/enzimologia , Hepatite B/enzimologia , Hepatite C/enzimologia , Neoplasias Hepáticas/enzimologia , Metaloproteinase 9 da Matriz/genética , Polimorfismo Genético , Sequência de Bases , Carcinoma Hepatocelular/etiologia , Estudos de Casos e Controles , Primers do DNA , Hepatite B/complicações , Hepatite C/complicações , Humanos , Neoplasias Hepáticas/complicações , Metaloproteinase 9 da Matriz/sangue , Regiões Promotoras Genéticas , Reação em Cadeia da Polimerase Via Transcriptase Reversa
5.
Arch Gynecol Obstet ; 288(5): 1035-8, 2013 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-23644921

RESUMO

OBJECTIVES: To evaluate the effect of immediate postpartum curettage on rapid resolution of clinical and laboratory indices in pre-eclampsia and eclampsia women. METHODS: A randomized controlled study, comprised of 420 pre-eclamptic or eclamptic women with singleton pregnancy 24 weeks gestation and more. Patients were divided into two groups: 220 patients underwent immediate postpartum curettage and 200 patients as a control group. RESULTS: The clinical and laboratory prenatal parameters showed no statistical significant differences between both groups. The follow-up for the postnatal clinical and laboratory data showed significant improvement for the mean arterial blood pressure in the curettage group over 6, 12, and 24 h after delivery and significant improvement in the platelet count as well. The average time required for MAP to reach 105 mmHg or less was significantly shorter (P < 0.05) in the curettage group (40 ± 3.15 h) than the control group (86 ± 5.34 h). Two patients in the curettage group developed convulsions versus 11 patients in the control group within the first 24 h after delivery. No maternal mortalities were reported in both groups. CONCLUSION: Immediate postpartum curettage is a safe and effective procedure and can accelerate recovery from pre-eclampsia or eclampsia.


Assuntos
Curetagem , Eclampsia/fisiopatologia , Eclampsia/cirurgia , Endométrio/cirurgia , Pré-Eclâmpsia/fisiopatologia , Pré-Eclâmpsia/cirurgia , Pressão Arterial , Feminino , Humanos , Contagem de Plaquetas , Período Pós-Parto , Gravidez , Fatores de Tempo
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