Rosa Priscila B, Neis Vivian B, Ribeiro Camille M, Moretti Morgana, Rodrigues Ana Lúcia S
Department of Biochemistry, Center of Biological Sciences, Universidade Federal de Santa Catarina, Florianópolis, 88040-900, SC, Brazil.
Post-Graduate Nutrition Program, Center of Health Sciences, Universidade Federal de Santa Catarina, Florianópolis, 88040-900, SC, Brazil.
Pharmacol Rep. 2016 Oct;68(5):996-1001. doi: 10.1016/j.pharep.2016.05.010. Epub 2016 Jul 15.
It has been suggested that dysregulation of γ-aminobutyric acid (GABA)-mediated neurotransmission is involved in the etiology of major depressive disorder and in the action of the fast-acting antidepressant ketamine. Considering that recent evidence has suggested that ascorbic acid may exert an antidepressant-like effect through mechanisms similar to ketamine, this study evaluated the involvement of GABAA and GABAB receptors in the antidepressant-like effect of ascorbic acid, comparing the results with those obtained with ketamine.
To investigate the involvement of GABAA in the antidepressant-like effect of ascorbic acid and ketamine in the tail suspension test (TST), mice were treated with a sub-effective dose of ascorbic acid (0.1mg/kg, po), ketamine (0.1mg/kg, ip) or vehicle and 30minutes later, a sub-effective dose of muscimol (0.1mg/kg, ip, GABAA receptor agonist) or vehicle was administered. In another set of experiments, mice were treated with ascorbic acid (1mg/kg, po, active dose in the TST) or vehicle and 30minutes later, baclofen (1mg/kg, ip, GABAB receptor agonist) was administered. A similar experimental protocol was performed with ketamine (1mg/kg, ip).
The administration of muscimol combined with ascorbic acid or ketamine produced a synergistic antidepressant-like effect in the TST. Moreover, the antidepressant-like effects of ascorbic acid and ketamine were abolished by baclofen. There was no alteration in spontaneous locomotion in any experimental group.
Results indicate that the anti-immobility effect of ascorbic acid and ketamine in TST may involve an activation of GABAA receptors and a possible inhibition of GABAB receptors.
有人提出,γ-氨基丁酸(GABA)介导的神经传递失调与重度抑郁症的病因及速效抗抑郁药氯胺酮的作用有关。鉴于最近有证据表明,抗坏血酸可能通过与氯胺酮类似的机制发挥抗抑郁样作用,本研究评估了GABAA和GABAB受体在抗坏血酸抗抑郁样作用中的参与情况,并将结果与氯胺酮的结果进行比较。
为了研究GABAA在抗坏血酸和氯胺酮在悬尾试验(TST)中的抗抑郁样作用中的参与情况,小鼠接受亚有效剂量的抗坏血酸(0.1mg/kg,口服)、氯胺酮(0.1mg/kg,腹腔注射)或溶剂处理,30分钟后,给予亚有效剂量的蝇蕈醇(0.1mg/kg,腹腔注射,GABAA受体激动剂)或溶剂。在另一组实验中,小鼠接受抗坏血酸(1mg/kg,口服,TST中的有效剂量)或溶剂处理,30分钟后,给予巴氯芬(1mg/kg,腹腔注射,GABAB受体激动剂)。对氯胺酮(1mg/kg,腹腔注射)进行了类似的实验方案。
蝇蕈醇与抗坏血酸或氯胺酮联合给药在TST中产生了协同抗抑郁样作用。此外,巴氯芬消除了抗坏血酸和氯胺酮的抗抑郁样作用。任何实验组的自发运动均无改变。
结果表明,抗坏血酸和氯胺酮在TST中的抗不动作用可能涉及GABAA受体的激活和对GABAB受体的可能抑制。