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王立琴, 朱树贞, 李德梅. 细叶远志皂甙对抑郁小鼠精神行为影响[J]. 中国公共卫生, 2020, 36(4): 570-573. DOI: 10.11847/zgggws1122400
引用本文: 王立琴, 朱树贞, 李德梅. 细叶远志皂甙对抑郁小鼠精神行为影响[J]. 中国公共卫生, 2020, 36(4): 570-573. DOI: 10.11847/zgggws1122400
Li-qin WANG, Shu-zhen ZHU, De-mei LI. Effect of tenuifolin on mental behavior in depression model mice[J]. Chinese Journal of Public Health, 2020, 36(4): 570-573. DOI: 10.11847/zgggws1122400
Citation: Li-qin WANG, Shu-zhen ZHU, De-mei LI. Effect of tenuifolin on mental behavior in depression model mice[J]. Chinese Journal of Public Health, 2020, 36(4): 570-573. DOI: 10.11847/zgggws1122400

细叶远志皂甙对抑郁小鼠精神行为影响

Effect of tenuifolin on mental behavior in depression model mice

  • 摘要:
      目的  探讨细叶远志皂甙(TEN)对抑郁小鼠精神行为的影响及机制。
      方法  将72只SPF级昆明小鼠随机分为对照组、模型组、阳性对照组及TEN 3、6、9 mg/kg组,每组12只;采用慢性不可预知轻度应激加孤养 28 d的方法复制小鼠抑郁症模型,灌胃给予不同剂量的TEN连续28 d, 测试各组小鼠强迫游泳实验和悬尾实验的不动时间;行为学测试后取脑,检测脑皮质5羟色胺(5-HT)含量和吲哚胺2, 3 – 双加氧酶(IDO)活性及海马乙酰胆碱酯酶(AchE)、胆碱乙酰转移酶(ChAT)活性。
      结果  与对照组比较,模型组小鼠强迫游泳实验和悬尾实验不动时间分别为(215.16 ± 18.39)和(182.89 ± 14.90)s均明显延长(均P < 0.01);与模型组比较,TEN 9 mg/kg组小鼠强迫游泳实验和悬尾实验不动时间分别为(183.64 ± 14.92)和(156.09 ± 12.38)s均明显缩短(均P < 0.05)。与对照组比较,模型组小鼠脑皮质内5-HT含量(28.96 ± 2.50)μg/L明显下降、IDO活性(11.87 ± 1.11)ng/mg明显增强(均P < 0.01);与模型组比较,TEN 9 mg/kg组小鼠脑皮质内5-HT含量(36.41 ± 3.32)μg/L明显升高、IDO活性(7.24 ± 0.71)ng/mg明显减弱(均P < 0.05)。与对照组比较,模型组小鼠脑海马组织中AchE活性(1.149 ± 0.218)U/mg明显增强、ChAT活性(50.44 ± 4.43)U/g明显减弱(均P < 0.01);与模型组比较,TEN 9 mg/kg组小鼠脑海马组织中AchE活性(0.584 ± 0.147)U/mg明显减弱、ChAT活性(86.05 ± 3.94)U/g明显增强(均P < 0.05)。
      结论  TEN对抑郁小鼠精神行为有一定的改善作用,其机制可能与小鼠脑皮质内5-HT表达升高、IDO表达下降及海马组织中AchE活性下降、ChAT活性升高有关。

     

    Abstract:
      Objective  To explore the effect and mechanism of tenuifolin (TEN) on mental behavior in depression model mice.
      Methods  Totally 72 specific pathogen free Kuming mice were randomly divided into 6 groups (12 in each group): a control and a model group treated with saline gavage, a positive control group with 3.5 mg/kg fluoxertine hydrochloride, and three TEN groups administered with TEN by gavage at doses of 3, 6, 9 mg/kg per day continuously for 4 weeks. The mouse depression model was established with chronic unpredictable mild stress and 28-day isolation method. At the end of the treatments, fixed time forced swimming and tail suspension test were performed for all the mice and then brain tissue samples of the mice were collected for measurements of 5-hydroxytryptamine (5-HT) content and the activity of indoleamine 2, 3-dioxygenase (IDO) in cerebral cortex and the activity of acetylcholinesterase (AchE) and choline acetyl-transferase (ChAT) in hippocampus.
      Results  Compared with those for the control mice, the fixed time of forced swimming test (215.16 ± 18.39 s) and tail suspension test (182.89 ± 14.90 s) were obviously prolonged the for the model mice (both P < 0.01). Compared with those for the model mice, the fixed time of forced swimming test (183.64 ± 14.92 s) and tail suspension test (156.09 ± 12.38 s) were shortened obviously for the mice treated with 9 mg/kg TEN (both P < 0.05). Lower content of 5-HT (28.96 ± 2.50 μg/L) but higher activity of IDO (11.87 ± 1.11 ng/mg) in cerebral cortex were detected in the model mice in comparison with those in the control mice (both P < 0.01). Significantly increased 5-HT content (36.41 ± 3.32 μg/L) and declined IDO activity (7.24 ± 0.71 ng/mg) in cerebral cortex were detected in the mice treated with 9 mg/kg TEN compared to those in the model mice (both P < 0.05). In comparison with those of the control mice, the AchE activity (1.149 ± 0.218 U/mg) increased but the ChAT activity (50.44 ± 4.43 U/g) declined significantly in hippocampus of the model mice (both P < 0.01). Significantly increased AchE activity (0.584 ± 0.147 U/mg) and decreased ChAT activity (86.05 ± 3.94 U/g) in hippocampus were detected in the mice treated with 9 mg/kg TEN compared to the model mice (both P < 0.05).
      Conclusion  To some extent, TEN can improve mental behavior in depression model mice; the mechanism may be related to the increased expression of 5-HT and decreased expression of IDO in cerebral cortex and the decreased activity of AchE and the increased activity of ChAT activity in hippocampal neurons of the mice.

     

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