Protective effect of morin hydrate against chronic unpredictable mild stress-induced depression in mice

Deepak , Dinesh Dhingra
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Abstract

Morin flavonoid has been reported to possess anti-stress, anti-anxiety, nootropic, anti-oxidant, and neuroprotective properties. In the present study, morin hydrate was evaluated for antidepressant-like activity in unstressed and stressed Swiss young male albino mice. The mice were subjected to chronic unpredictable mild stress (CUMS) for 21 successive days. Morin hydrate (10, 20, and 40 mg/kg, p.o.) and fluoxetine (20 mg/kg, p.o.) per se were administered for 21 successive days to separate groups of unstressed and stressed mice. Tail suspension test (TST) and sucrose preference test were used to evaluate the effect of Morin on depression-like behavior in mice. During the study, the effect of Morin on lipid peroxidation, reduced glutathione, catalase, nitrite, corticosterone, and MAO-A activity was estimated. All the results were analyzed by analysis of variance (ANOVA) followed by the Tukey–Kramer multiple comparison test using Graph Pad Instat (GPIS) package, version 3.05. Morin (20 and 40 mg/kg, p.o.) per se administered for 21 successive days significantly decreased the immobility period of stressed mice in the tail suspension test as compared to vehicle-treated stressed mice, indicating significant antidepressant-like activity. Morin significantly restored the reduced sucrose preference (%) in stressed mice as compared to vehicle-treated stressed mice. Further, morin significantly reversed the stress-induced increase in brain thiobarbituric acid-reactive substances (TBARS), plasma nitrite, and corticosterone levels, and increased the stress-induced decrease in brain catalase levels. The highest dose (40 mg/kg) of morin hydrate significantly inhibited brain MAO-A activity in stressed mice. Thus, morin hydrate showed significant antidepressant-like activity in mice subjected to CUMS, probably through inhibition of brain MAO-A activity, decrease in plasma nitrite and corticosterone levels, and due to its antioxidant activity.
水合桑苷对小鼠慢性不可预测的轻度应激性抑郁症的保护作用
据报道,Morin类黄酮具有抗应激、抗焦虑、促智、抗氧化和神经保护特性。在本研究中,水合桑里酯对无压力和有压力的瑞士年轻雄性白化小鼠的抗抑郁活性进行了评估。小鼠连续21天遭受慢性不可预测轻度应激(CUMS)。将水合桑苷(10、20和40 mg/kg, p.o.)和氟西汀(20 mg/kg, p.o.)分别给予非应激组和应激组小鼠连续21天。采用悬尾试验(TST)和蔗糖偏好试验评价桑苷对小鼠抑郁样行为的影响。在研究中,估计了桑辣素对脂质过氧化、还原性谷胱甘肽、过氧化氢酶、亚硝酸盐、皮质酮和MAO-A活性的影响。所有结果采用方差分析(ANOVA)进行分析,然后使用graphpad Instat (GPIS)软件包进行Tukey-Kramer多重比较检验,版本为3.05。与车辆处理的应激小鼠相比,连续给药21天的莫兰素(20和40 mg/kg, p.o.)显著减少了小鼠在悬尾试验中的静止时间,显示出明显的抗抑郁样活性。与给药小鼠相比,桑辣素显著恢复了应激小鼠对蔗糖的偏好(%)。此外,桑肽显著逆转应激诱导的脑硫代巴比妥酸反应物质(TBARS)、血浆亚硝酸盐和皮质酮水平的升高,并增加应激诱导的脑过氧化氢酶水平的降低。最高剂量(40 mg/kg)的莫里素水合物显著抑制应激小鼠脑MAO-A活性。因此,水合桑苷在小鼠CUMS中表现出显著的抗抑郁样活性,可能是通过抑制大脑MAO-A活性,降低血浆亚硝酸盐和皮质酮水平,以及由于其抗氧化活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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