Translational Psychiatry Laboratory, Graduate Program in Health Sciences, University of Southern Santa Catarina (UNESC), Criciúma, SC, Brazil.
Experimental Neurology Laboratory, Graduate Program in Health Sciences, Health Sciences Unit, University of Southern Santa Catarina, Criciúma, SC, Brazil.
Brain Res Bull. 2021 Jul;172:129-138. doi: 10.1016/j.brainresbull.2021.04.021. Epub 2021 Apr 28.
This study aimed to evaluate the effects of ketamine, on behavioral parameters, oxidative stress, and inflammation in the brain of male and female rats submitted to the animal model of maternal deprivation (MD). Wistar rats were deprived of maternal care in the first 10 days of life (three hours daily). As adults, male and female rats were divided: control + saline deprived + saline and deprived + ketamine (15 mg/kg). The behavior was evaluated through the open field and forced swimming tests. Then brain was removed for analysis of oxidative damage, the activity of superoxide dismutase (SOD), catalase (CAT), and myeloperoxidase (MPO) activity, and levels of interleukin-6 (IL-6). MD induced depressive behavior in males and ketamine reversed these changes. MD induced an increase in lipid peroxidation in males and females; ketamine reversed these effects in males. Protein carbonylation was increased in males and females, with ketamine decreasing such effects. The concentration of nitrite/nitrate increased in males and females, whereas ketamine decreased this in the PFC of males. SOD and CAT activities were decreased in male and female deprived groups and deprived groups treated with ketamine. MPO activity and IL-6 levels increased in males subjected to MD and ketamine reversed this effect. The results suggest that stressful events in early life can induce behavioral, neuroimmune changes, and oxidative stress, however, such effects depend on sex and brain area. Ketamine presents anti-inflammatory and antioxidant properties and could be considered an alternative for individuals who are resistant to classical treatments.
本研究旨在评估氯胺酮对经历了母体剥夺(MD)动物模型的雄性和雌性大鼠的行为参数、氧化应激和大脑炎症的影响。Wistar 大鼠在生命的头 10 天(每天三小时)被剥夺了母性照顾。成年后,雄性和雌性大鼠被分为:对照组+生理盐水剥夺+生理盐水和剥夺+氯胺酮(15mg/kg)。通过旷场和强迫游泳试验评估行为。然后取出大脑,分析氧化损伤、超氧化物歧化酶(SOD)、过氧化氢酶(CAT)和髓过氧化物酶(MPO)活性以及白细胞介素-6(IL-6)的水平。MD 诱导雄性大鼠出现抑郁行为,而氯胺酮逆转了这些变化。MD 导致雄性和雌性大鼠的脂质过氧化增加;氯胺酮逆转了这些影响。雄性和雌性大鼠的蛋白质羰基化增加,而氯胺酮降低了这种作用。雄性和雌性大鼠的亚硝酸盐/硝酸盐浓度增加,而氯胺酮降低了 PFC 中的这种浓度。SOD 和 CAT 活性在雄性和雌性剥夺组以及接受氯胺酮治疗的剥夺组中降低。MPO 活性和 IL-6 水平在经历 MD 和氯胺酮的雄性大鼠中升高,而氯胺酮逆转了这种效应。结果表明,早期生活中的应激事件会导致行为、神经免疫和氧化应激的变化,但这些影响取决于性别和大脑区域。氯胺酮具有抗炎和抗氧化特性,可被视为对经典治疗有抗性的个体的替代治疗方法。