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1.
PLoS One ; 14(9): e0222698, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-31545844

RESUMO

The osmotic stability of the erythrocyte membrane (OSEM) has been associated with changes in lipid profile, blood glucose and blood pressure. Changes in these parameters are very frequent in shift workers, possibly because of the lack of synchronization of biological rhythms, which results in the social jetlag. However, the existence of association between OSEM and circadian misalignment has not been investigated in this population. Therefore, this study investigated whether shift work, sleep time and social jetlag (SJL) are associated with biochemical and hematological variables. A population consisting of 79 men working at night (n = 37) or during the day (n = 42), aged between 21 and 65 years and with a mean BMI of 27.56 ± 4.0 kg/m2, was investigated cross-sectionally in relation to sleep time, SJL, anthropometric (height, weight and waist circumference) and blood variables, with emphasis on the OSEM. SJL was calculated by the absolute difference between the midpoint of sleep on work and rest days. The Generalized Linear Model (GzLM) was used to investigate the existence of associations between SJL and average sleep time in relation to the analyzed variables. Workers without SJL presented lower baseline lysis values of erythrocytes in isotonic medium in relation to workers with SJL. In addition, workers who slept on average less than 6 hours had higher OSEM, and higher total and LDL-cholesterol in relation to those who slept more than 6 hours, regardless of the shift. It is possible that the association of sleep deprivation and SJL with erythrocyte membrane stability is mediated through changes in the lipid profile.


Assuntos
Membrana Eritrocítica/fisiologia , Jornada de Trabalho em Turnos/efeitos adversos , Sono/fisiologia , Adulto , Idoso , Estudos Transversais , Humanos , Síndrome do Jet Lag/sangue , Síndrome do Jet Lag/fisiopatologia , Masculino , Pessoa de Meia-Idade , Privação do Sono/sangue , Privação do Sono/fisiopatologia , Adulto Jovem
2.
Diabetes Res Clin Pract ; 144: 153-160, 2018 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-29427698

RESUMO

OBJECTIVES: This study aimed to evaluate the correlations of glycemic variability with erythrocyte membrane stability parameters and oxidative stress markers in patients with type 1 diabetes mellitus (T1DM) under intensive treatment. MATERIAL AND METHODS: 90 patients with T1DM and under intensive treatment of the disease were evaluated in relation to anthropometric indices, records of glycemic averages and parameters of glycemic variability, biochemical dosages (glucose, uric acid, lipidogram, glycated hemoglobin, microalbuminuria, creatinine and iron) reticulocyte count, erythrocyte membrane stability parameters and oxidative stress markers (thiobarbituric acid reactive substances, TBARS, and glutathione reductase, GR). RESULTS: Indicators of glycemic variability in the short and long term showed correlations with parameters of membrane stability and markers of oxidative stress (GR). In addition, the comparison of these same parameters between the subgroups consisting of quartiles of GV or glycemic control also showed significant differences. CONCLUSION: In the T1DM patients studied here, glycemic variability showed correlations with oxidative stress and erythrocyte membrane stability variables. This corroborates the hypothesis that glycemic fluctuations interfere with lipid peroxidation and cell membrane behavior, emphasizing its participation in mechanisms related to the development of chronic complications of diabetes.


Assuntos
Diabetes Mellitus Tipo 1/fisiopatologia , Membrana Eritrocítica/patologia , Índice Glicêmico/efeitos dos fármacos , Hipoglicemiantes/uso terapêutico , Estresse Oxidativo/efeitos dos fármacos , Adulto , Biomarcadores/metabolismo , Glicemia/metabolismo , Estudos Transversais , Diabetes Mellitus Tipo 1/sangue , Diabetes Mellitus Tipo 1/tratamento farmacológico , Membrana Eritrocítica/efeitos dos fármacos , Feminino , Hemoglobinas Glicadas/metabolismo , Humanos , Peroxidação de Lipídeos/efeitos dos fármacos , Masculino
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