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1.
Cutan Ocul Toxicol ; 40(3): 198-206, 2021 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-33653184

RESUMO

PURPOSE: Rapid development in mobile phone technologies increase the average mobile phone usage duration. This increase also triggers exposure to radiofrequency radiation (RF), which is a risk factor for the health. In this study, it was aimed to investigate the effect of mobile phone working with LTE-Advanced Pro (4.5 G) mobile network on the optic nerve, which is responsible for the transmission of visual information. MATERIAL AND METHODS: Thirty-two rats divided into two groups as control (no RF, sham exposure) and experimental (RF exposure using a mobile phone with LTE-Advanced Pro network; 2 hours/day, 6 weeks). The visual evoked potential (VEP) was recorded and determined amplitudes and latencies of VEP waves. Optic nerve malondialdehyde level, catalase and superoxide dismutase activities were determined. Furthermore, ultrastructural and morphometric changes of optic nerve were evaluated. RESULTS: In VEP recordings, the mean VEP amplitudes of experimental group were significantly lower than control group. In ultrastructural evaluation, myelinated nerve fibres and glial cells were observed in normal histologic appearance both in sham and experimental group. However, by performing morphometric analysis, in the experimental group, axonal diameter and myelin thickness were shown to be lower and the G-ratio was higher than in the sham group. In the experimental group, malondialdehyde level was significantly higher and superoxide dismutase and catalase activities were significantly lower than sham group. There was a high correlation between VEP wave amplitudes and oxidative stress markers. CONCLUSION: Findings obtained in this study support optic nerve damage. These results point out an important risk that may decrease the quality of life.


Assuntos
Telefone Celular , Traumatismos do Nervo Óptico/etiologia , Nervo Óptico/efeitos da radiação , Ondas de Rádio/efeitos adversos , Animais , Modelos Animais de Doenças , Relação Dose-Resposta à Radiação , Potenciais Evocados Visuais/efeitos da radiação , Humanos , Masculino , Nervo Óptico/patologia , Traumatismos do Nervo Óptico/patologia , Estresse Oxidativo/efeitos da radiação , Ratos
2.
Cereb Cortex ; 17(5): 1007-19, 2007 May.
Artigo em Inglês | MEDLINE | ID: mdl-16751296

RESUMO

Gamma oscillations (30-80 Hz) have been demonstrated to be important for perceptual and cognitive processes. Animal and in vitro studies have revealed possible underlying generation mechanisms of the gamma rhythm. However, little is known about the neurochemical modulation of these oscillations during human cognition. Schizophrenia and Attention Deficit Hyperactivity Disorder, which lead to failure of attentional modulation and working memory, introduce significant changes in gamma responses and have significant associations with genetic polymorphisms of dopamine receptor D4 (DRD4), dopamine transporter (DAT), and catechol-O-methyltransferase (COMT). Therefore, the presence of direct relations between these polymorphisms and gamma oscillations was investigated in human subjects using an auditory target detection paradigm. The 7-repeat isoform of the DRD4 polymorphism that produces a subsensitive variant of the D4 receptor enhanced the auditory evoked and induced gamma responses to both standard and target stimuli. The 10/10 genotype of the DAT1 polymorphism, which reduces DAT expression and hence yields an increase in extracellular dopamine, specifically enhanced evoked gamma responses to target stimuli. The COMT polymorphism did not significantly change gamma responses. It seems plausible to assume that the modulation pattern of the evoked gamma response by DRD4 polymorphism relates to reduced inhibition via the D4 receptor, whereas the DAT1 effect is related to the target detection mechanism probably mediated by the D1 receptor.


Assuntos
Córtex Auditivo/fisiologia , Relógios Biológicos/fisiologia , Proteínas da Membrana Plasmática de Transporte de Dopamina/genética , Eletroencefalografia/métodos , Potenciais Evocados Auditivos/fisiologia , Receptores de Dopamina D4/genética , Localização de Som/fisiologia , Adaptação Fisiológica/genética , Adulto , Humanos , Masculino , Polimorfismo de Nucleotídeo Único/genética
3.
Biochem Biophys Res Commun ; 340(2): 417-21, 2006 Feb 10.
Artigo em Inglês | MEDLINE | ID: mdl-16375858

RESUMO

Agonist and depolarization-induced vascular smooth muscle contractions include the activation of rho/rho kinase pathway. However, there are no reports addressing the question whether this pathway is involved in ouabain-induced vascular smooth muscle contractions. Therefore, in this study, the possible participation of the rho/rho kinase pathway in ouabain-induced contractions was evaluated in rat renal arteries. Effects of rho kinase inhibitors (fasudil and Y-27632) on ouabain-induced contractions, and phosphorylation of myosin binding subunits (MYPT/MBS85) of myosin phosphatase were determined using isolated tissue and Western blot experiments, respectively. Fasudil and Y-27632 inhibited ouabain-induced contractions in a concentration-dependent manner. The phosphorylation of MYPT was not altered by ouabain. However, ouabain significantly increased MBS85 phosphorylation of myosin phosphatase. The phosphorylation of both subunits of myosin phosphatase was inhibited by Y-27632. These results indicate that activation of rho kinase and the subsequent phosphorylation of MBS85 are involved in ouabain-induced contraction of rat renal arteries. This mechanism may be important in essential hypertension with elevated endogenous ouabain levels.


Assuntos
Ouabaína/farmacologia , Proteínas Serina-Treonina Quinases/fisiologia , Artéria Renal/efeitos dos fármacos , Vasoconstrição/efeitos dos fármacos , Amidas/farmacologia , Animais , Inibidores Enzimáticos/farmacologia , Peptídeos e Proteínas de Sinalização Intracelular , Isoenzimas/antagonistas & inibidores , Isoenzimas/biossíntese , Isoenzimas/genética , Isoenzimas/fisiologia , Masculino , Músculo Liso Vascular/efeitos dos fármacos , Músculo Liso Vascular/fisiologia , Fosfatase de Miosina-de-Cadeia-Leve/metabolismo , Fosforilação , Proteínas Serina-Treonina Quinases/antagonistas & inibidores , Piridinas/farmacologia , Ratos , Ratos Wistar , Artéria Renal/enzimologia , Quinases Associadas a rho
4.
Brain Res Cogn Brain Res ; 20(3): 376-83, 2004 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-15268915

RESUMO

The effects of the changes in the frequency spectrum of the electroencephalogram (EEG) on the perception of near-threshold visual stimuli and on the event-related potentials (ERPs) produced by these stimuli were investigated on 12 healthy volunteers. The stimulus intensity, at which each subject could detect 50% of the presented stimuli, was defined as the sensory threshold for that subject. Single ERP trials were separated into two groups: trials with detected and undetected stimuli. The ERPs and the average power spectra of the 1 s prestimulus periods were computed for both conditions. P300 amplitudes of the ERPs, and total power and relative band powers of the delta (0.5-4 Hz), theta (4-7.5 Hz), alpha (7.5-13 Hz), beta (13-30 Hz), and gamma (30-70 Hz) frequency bands of the prestimulus power spectra were measured. Between the two conditions, a specific difference was observed in the relative power of the alpha band, which was significantly lower before detected stimuli (p < 0.01) in line with significantly higher amplitudes of the ERPs (p < 0.001). These results show that short-lasting changes in brain's excitability state are reflected the relative alpha power of the EEG, which may explain significant variability in perceptual processes and ERP generation especially at boundary conditions such as sensory threshold.


Assuntos
Ritmo alfa , Potenciais Evocados Visuais/fisiologia , Córtex Visual/fisiologia , Percepção Visual/fisiologia , Adulto , Potenciais Evocados P300/fisiologia , Feminino , Humanos , Masculino , Limiar Sensorial/fisiologia
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