Laboratório de Neurociências, Unidade Acadêmica em Ciências da Saúde, Universidade do Extremo Sul Catarinense, Criciúma, SC, Brazil.
Laboratório de Fisiopatologia Clínica e Experimental, Universidade do Sul de Santa Catarina, Tubarão, SC, Brazil.
Brain Res Bull. 2018 Mar;137:204-216. doi: 10.1016/j.brainresbull.2017.12.005. Epub 2017 Dec 15.
Despite decades of research, the fundamental neurochemical and molecular mechanisms underlying the major depressive disorder (MDD) are still poorly understood, and current antidepressant treatments have limited clinical efficacy. In clinical conditions, the rapprochement between the disease and the corrective actions of drugs in laboratory animals is essential for developing effective therapies. Thus, the aim of this study was to evaluate the antidepressant effects of ketamine (N-metil-d-asparte (NMDA) receptor antagonist), minocycline (tetracycline antibiotic), and amitriptyline (classical antidepressant), on behavior and oxidative stress parameters in animals submitted to the chronic mild stress (CMS) and maternal deprivation protocols. For this aim, male Wistar rats were submitted to maternal deprivation or CMS. To induce maternal deprivation, Wistar rats were deprived of maternal care during the first 10 days of life. To induce CMS, Wistar rats were submitted to the CMS for 40 days. To reverse the effects of stress, treatment was done intraperitoneally with a single dose of ketamine (15 mg/kg), and minocycline (25 mg/kg) and amitriptyline (10 mg/kg) by 20 days. After treatment, the animals were submitted to the forced swimming test and then analyzed oxidative stress parameters in the prefrontal cortex (PFC), hippocampus, amygdala and nucleus accumbens (NAc). Treatment with ketamine, minocycline and amitriptyline were able to exert antidepressant effects in the forced swimming test. However, these antidepressant effects were dependent on the stress model by which the animals were exposed. In certain brain regions some treatment strategies had a pro-oxidant effect. Though, most of the strategies used in this study had antioxidant effects, as reported by a decrease on protein and lipid damage, nitrite/nitrate concentration and myeloperoxidase activity. In addition, an increase in the antioxidant superoxide dismutase (SOD) and catalase (CAT) enzymes activities were also evident after treatments. In conclusion, the antidepressant effects of ketamine and minocycline, in the present study, may be associated, at least in part, with its antioxidant and neuroprotective effects in animals subjected to maternal deprivation or CMS.
尽管经过了几十年的研究,但导致重度抑郁症(MDD)的基本神经化学和分子机制仍未得到很好的理解,而目前的抗抑郁治疗方法的临床疗效有限。在临床情况下,将疾病与实验室动物中药物的矫正作用联系起来,对于开发有效的治疗方法至关重要。因此,本研究的目的是评估氯胺酮(N-甲基-D-天冬氨酸(NMDA)受体拮抗剂)、米诺环素(四环素抗生素)和阿米替林(经典抗抑郁药)对慢性轻度应激(CMS)和母婴分离模型动物的行为和氧化应激参数的抗抑郁作用。为此,雄性 Wistar 大鼠接受了母婴分离或 CMS 处理。为了诱导母婴分离,Wistar 大鼠在生命的前 10 天内被剥夺了母性照顾。为了诱导 CMS,Wistar 大鼠接受了 40 天的 CMS 处理。为了逆转应激的影响,通过腹膜内注射给予单次剂量的氯胺酮(15mg/kg)、米诺环素(25mg/kg)和阿米替林(10mg/kg),共 20 天。治疗后,动物被进行强迫游泳测试,然后分析前额叶皮质(PFC)、海马、杏仁核和伏隔核(NAc)中的氧化应激参数。氯胺酮、米诺环素和阿米替林的治疗能够在强迫游泳测试中发挥抗抑郁作用。然而,这些抗抑郁作用取决于动物暴露的应激模型。在某些脑区,某些治疗策略具有促氧化作用。尽管如此,本研究中使用的大多数策略都具有抗氧化作用,如蛋白和脂质损伤、亚硝酸盐/硝酸盐浓度和髓过氧化物酶活性的降低。此外,治疗后还明显增加了抗氧化超氧化物歧化酶(SOD)和过氧化氢酶(CAT)酶的活性。综上所述,本研究中氯胺酮和米诺环素的抗抑郁作用可能至少部分与其在母婴分离或 CMS 处理动物中的抗氧化和神经保护作用有关。