Laboratory of Neuronal Signaling and Psychopharmacology, Graduate Program in Health Sciences, Health Sciences Unit, University of Southern Santa Catarina (UNESC), Criciúma, SC, Brazil.
Laboratory of Neurosciences, Graduate Program in Health Sciences, Health Sciences Unit, University of Southern Santa Catarina (UNESC), Criciúma, SC, Brazil.
Bipolar Disord. 2017 Jun;19(4):246-258. doi: 10.1111/bdi.12503. Epub 2017 Jun 14.
The goal of the present study was to investigate the effects of lithium administration on behavior, oxidative stress parameters and cytokine levels in the periphery and brain of mice subjected to an animal model of mania induced by paradoxical sleep deprivation (PSD).
Male C57 mice were treated with saline or lithium for 7 days. The sleep deprivation protocol started on the 5th day during for the last 36 hours of the treatment period. Immediately after the sleep deprivation protocol, animals locomotor activity was evaluated and serum and brain samples was extracted to evaluation of corticosterone and adrenocorticotropic hormone circulating levels, oxidative stress parameters and citokynes levels.
The results showed that PSD induced hyperactivity in mice, which is considered a mania-like behavior. PSD increased lipid peroxidation and oxidative damage to DNA, as well as causing alterations to antioxidant enzymes in the frontal cortex, hippocampus and serum of mice. In addition, PSD increased the levels of cytokines in the brains of mice. Treatment with lithium prevented the mania-like behavior, oxidative damage and cytokine alterations induced by PSD.
Improving our understanding of oxidative damage in biomolecules, antioxidant mechanisms and the inflammatory system - alterations presented in the animal models of mania - is important in helping us to improve our knowledge concerning the pathophysiology of BD, and the mechanisms of action employed by mood stabilizers.
本研究旨在探讨锂对匹莫齐特睡眠剥夺(PSD)诱导的躁狂动物模型中小鼠行为、氧化应激参数和外周及大脑细胞因子水平的影响。
雄性 C57 小鼠用生理盐水或锂处理 7 天。睡眠剥夺方案在治疗期的最后 36 小时内开始于第 5 天。睡眠剥夺方案结束后,立即评估动物的运动活性,并提取血清和脑组织样本,以评估循环皮质酮和促肾上腺皮质激素水平、氧化应激参数和细胞因子水平。
结果表明,PSD 诱导小鼠出现多动,这被认为是一种类似于躁狂的行为。PSD 增加了脂质过氧化和 DNA 氧化损伤,并导致小鼠额叶皮质、海马体和血清中的抗氧化酶发生改变。此外,PSD 还增加了小鼠大脑中的细胞因子水平。锂治疗可预防 PSD 诱导的类似躁狂的行为、氧化损伤和细胞因子改变。
了解生物分子、抗氧化机制和炎症系统中的氧化损伤——这些在躁狂动物模型中出现的改变——对于帮助我们提高对双相情感障碍的病理生理学以及心境稳定剂作用机制的认识非常重要。