Effects of paradoxical sleep deprivation on oxidative parameters in the serum and brain of mice submitted to the animal model of hyperglycemia

被引:0
|
作者
Da Rosa, Julia Panato- [1 ]
Sandrini, Isadora Gava [1 ]
Possamai-Della, Taise [1 ]
Aguiar-Geraldo, Jorge M. [1 ]
-Laureano, Maria Luisa Machado [1 ]
Zugno, Alexandra I. [1 ]
Quevedo, Joa [1 ,2 ,3 ,4 ]
Valvassori, Samira S. [1 ]
机构
[1] Univ Southern Santa Catarina UNESC, Grad Program Hlth Sci, Translat Psychiat Lab, Criciuma, SC, Brazil
[2] Univ Texas Hlth Sci Ctr Houston UTHealth, McGovern Med Sch, Faillace Dept Psychiat & Behav Sci, Translat Psychiat Program, Houston, TX USA
[3] Univ Texas Hlth Sci Ctr Houston UTHealth, Ctr Excellence Mood Disorders, McGovern Med Sch, Faillace Dept Psychiat & Behav Sci, Houston, TX USA
[4] Univ Texas Hlth Sci Ctr Houston UTHealth Houston, Ctr Intervent Psychiat, McGovern Med Sch, Faillace Dept Psychiat & Behav Sci, Houston, TX USA
关键词
Diabetes; Sleep disorders; Oxidative stress; HPA axis; DEPRESSIVE-LIKE BEHAVIOR; BIPOLAR DISORDER; STRESS; INHIBITION; ACTIVATION; AMYGDALA; CORTEX; ASSAY;
D O I
10.1016/j.bbr.2024.115008
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
The present study aimed to investigate the effects of paradoxical sleep deprivation (PSD) on behavioral and oxidative stress parameters in the brain and serum of mice submitted to the animal model of hyperglycemia induced by alloxan, mimicking the main symptom of diabetes mellitus (DM). Adults C57BL/6 male and female mice received an injection of alloxan, and ten days later, the animals were submitted to the PSD for 36 h. The animals' behavioral parameters were evaluated in the open-field test. Oxidative stress parameters [Diacetyldichlorofluorescein (DCF), Thiobarbituric acid reactive substances (TBARS), Superoxide dismutase (SOD), and Glutathione] were assessed in the frontal cortex, hippocampus, striatum, and serum. The PSD increased the male and female mice locomotion, but the alloxan's pre-administration prevented the PSD-induced hyperactivity. In addition, the male mice receiving alloxan and submitted to the PSD had elevated latency time in the first quadrant and the number of fecal boli, demonstrating increased anxiety-like behavior. The HPA-axis was hyperactivating in male and female mice pre-administered alloxan and/or PSD-submitted animals. The oxidative stress parameters were also increased in the serum of the animals administered alloxan and/or sleep-deprived mice. Despite alloxan or PSD leading to behavioral or biochemical alterations, the one did not potentiate the other in mice. However, more studies are necessary to identify the link between sleep and hyperglycemia.
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页数:11
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