Liao Jung-Chun, Tsai Jen-Chieh, Liu Chia-Yu, Huang Hui-Chi, Wu Lung-Yuan, Peng Wen-Huang
Department of Chinese Pharmaceutical Sciences and Chinese Medicine Resources, College of Pharmacy, China Medical University, No, 91, Hsueh-Shih Road, Taichung 404, Taiwan.
BMC Complement Altern Med. 2013 Nov 1;13:299. doi: 10.1186/1472-6882-13-299.
The present study was undertaken to evaluate the anti-depressive activity of turmerone after one-week administration by using a mouse forced swimming test (FST) and tail suspension test (TST).
Animals were divided into four groups (n = 10 /group): control (0.9% saline), the three doses of turmerone (1.25, 2.5, 5.0 mg/kg) for one-week treatment. To assess the effect of turmerone on locomotor activity, mice were evaluated in the open-field paradigm. Forced swimming test (FST) and Tail suspension test (TST) were used to take as a measure of antidepressant activity. The probable mechanisms of action of the anti-depressive effect of turmerone was also investigated by measuring the activity of monoamine oxidase-A and corticosterone levels in the blood and the levels of monoamines in the cortex, striatum, hippocampus and hypothalamus of the mice.
Turmerone (2.5, 5.0 mg/kg, p.o.) significantly reduced the immobility time of mice in both the FST and TST, but it did not significantly affect the ambulatory and total movements of mice. However, hyperactivity might explain the results. In addition, turmerone decreased the corticosterone level in the blood while it increased the levels of 5-HT in cortex, striatum, hippocampus, and hypothalamus, the level of NE in striatum and hippocampus, the levels of MHPG and DOPAC in hypothalamus, the level of 5-HIAA in striatum, and the level of DA in striatum, hippocampus, and hypothalamus. Turmerone (2.5, 5.0 mg/kg) decreased the activity of MAO-A in the frontal cortex and hippocampus of mouse brain.
After one-week administration, turmerone produced antidepressant-like effects. The mechanisms of action of anti-depressive effect of turmerone seemed to involve an increase of the monoamines level decreasing the MAO-A activity and the stress of mice.
本研究旨在通过小鼠强迫游泳试验(FST)和悬尾试验(TST)评估姜黄烯连续给药一周后的抗抑郁活性。
将动物分为四组(每组n = 10):对照组(0.9%生理盐水),三个剂量的姜黄烯(1.25、2.5、5.0 mg/kg)进行为期一周的治疗。为评估姜黄烯对运动活性的影响,在旷场范式中对小鼠进行评估。强迫游泳试验(FST)和悬尾试验(TST)用于衡量抗抑郁活性。还通过测量小鼠血液中单胺氧化酶 - A的活性、皮质酮水平以及大脑皮质、纹状体、海马体和下丘脑中单胺的水平,研究姜黄烯抗抑郁作用的可能作用机制。
姜黄烯(2.5、5.0 mg/kg,口服)显著缩短了小鼠在FST和TST中的不动时间,但对小鼠的自主活动和总活动没有显著影响。然而,多动可能解释了这些结果。此外,姜黄烯降低了血液中的皮质酮水平,同时增加了皮质、纹状体、海马体和下丘脑中5 - HT的水平,纹状体和海马体中NE的水平,下丘脑中MHPG和DOPAC的水平,纹状体中5 - HIAA的水平,以及纹状体、海马体和下丘脑中DA的水平。姜黄烯(2.5、5.0 mg/kg)降低了小鼠大脑额叶皮质和海马体中MAO - A的活性。
连续给药一周后,姜黄烯产生了类似抗抑郁的作用。姜黄烯抗抑郁作用的作用机制似乎涉及单胺水平的增加、MAO - A活性的降低以及小鼠应激的减轻。