Sleep Deprivation Models in Rodents (Model Kekurangan Tidur dalam Roden) / Jurnal Sains Kesihatan Malaysia

@#Sleep deprivation has been identified as a risk factor for various diseases. The number of patients suffering from sleep deprivation is increasing daily. Therefore, the risk to develop various diseases, including cardiovascular disease is increasing. However, there is a limitation to elucidate the pathophysiological changes following sleep deprivation in humans. Thus, the need arises for sleep deprivation models using animals, which will serve the purpose of understanding the disease in a better way. Several techniques have been developed to model sleep deprivation in animals, including inverted flowerpot and multiple platforms techniques. Genetic and environmental factors, costs, infrastructure and animal life spans are some of the factors that need to be considered when selecting a particular model. Furthermore, when studying sleep deprivation, tissue samples, such as peripheral blood, brain samples and aorta are used to elucidate the underlying mechanisms of a particular disease. Currently, more than ninety percent of all laboratory animal experiments are performed in rats and mice. This review article focuses on models of sleep deprivation in Rodents, which are generally used in research laboratories. The article also tries to evaluate the advantages and disadvantages of each technique discussed, guides the sleep deprivation model and helps researchers to decide on a specific model for their purpose.

Impact of deep slow-wave sleep deprivation on oxidative stress response of the testis tissue in rats / 中华男科学杂志

Objective@#To investigate the influence of deep slow-wave sleep deprivation on the oxidative stress of testicular tissue in rats.@*METHODS@#Thirty-six 5-week-old male Wistar rats were equally randomized into deep slow-wave sleep deprivation group (SD1), deep slow-wave sleep and duration sleep deprivation group ( SD2), and a cage control group (CC). The rat model of deep slow-wave sleep deprivation was established using the flowerpot technique. The rats in the SD1 group were interfered every 24 minutes and deprived of 12 hours of sleep at night, those in the SD2 group deprived of 8 minutes of sleep at an interval of 24 minutes and 12 hours of sleep at night, and those in the CC group exposed to 12 hours of daylight and 12 hours of darkness. After 28 days, all the rats were executed for measurement of the testis volume and protein content, determination of the methane dicarboxylic aldehyde (MDA) level and activities of superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px), and observation of the pathological changes in the testicular tissue under the microscope.@*RESULTS@#Compared with the CC group, the rats in the SD1 and SD2 groups showed significantly reduced body weight (［268.5 ± 1.6］ vs ［248.1 ± 25.1］and［232.9 ± 10.1］g, P0.05). The lumens in the testis were narrowed, with obvious hyperplasia, hyperemia and edema in the peripheral interstitial tissue, but no significant pathologic changes were observed in the testis tissue of the SD1 group.@*CONCLUSIONS@#Long-term deprivation of deep slow-wave sleep impairs the structure of the testis tissue and induces oxidative stress response in rats.