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熊果酸可阻断慢性不可预知应激诱导的抑郁样行为和海马促凋亡失衡。

Ursolic acid abrogates depressive-like behavior and hippocampal pro-apoptotic imbalance induced by chronic unpredictable stress.

机构信息

Department of Biochemistry, Center of Biological Sciences, Universidade Federal de Santa Catarina, Florianópolis, 88040-900, SC, Brazil.

出版信息

Metab Brain Dis. 2021 Mar;36(3):437-446. doi: 10.1007/s11011-020-00658-4. Epub 2021 Jan 4.

DOI:10.1007/s11011-020-00658-4
PMID:33394285
Abstract

Emerging evidence has shown that ursolic acid exerts antidepressant-like effects, however, its ability to elicit an antidepressant-like response in rodents subjected to stress model that mimics behavioral and neurochemical alterations found in depression remains to be determined. Thus, this study investigated the possible antidepressant-like effect of ursolic acid in mice subjected to chronic unpredictable stress (CUS) for 14 days, and whether this effect could be associated with the modulation of serum corticosterone levels and hippocampal Bcl-2/Bax mRNA expression. Our results indicated that CUS induced a depressive-like behavior, as demonstrated by an increase in the immobility time and latency to first grooming in the tail suspension test and splash test, respectively. Conversely, the repeated administration of ursolic acid (0.1 mg/kg, p.o.) or fluoxetine (10 mg/kg, p.o.) in the last 7 days of CUS completely prevented CUS-induced behavioral alterations, suggesting an antidepressant-like effect. Additionally, CUS significantly increased the mRNA expression of Bax (pro-apoptosis marker), but not Bcl-2 (anti-apoptosis marker) in the hippocampus. Moreover, reduced hippocampal mRNA expression of Bcl-2/Bax ratio was detected in CUS-exposed mice. Ursolic acid, but not fluoxetine, prevented CUS-induced increase in the expression of Bax, but both ursolic acid and fluoxetine prevented CUS-induced reduction on Bcl-2/Bax ratio. Furthermore, neither CUS nor treatments with ursolic acid or fluoxetine altered serum corticosterone levels. Our study unveils the ability of ursolic acid to prevent the depressive-like behavior induced by stress and the modulation of Bcl-2/Bax expression could be associated with this response.

摘要

新出现的证据表明,熊果酸具有抗抑郁作用,然而,其在应激模型中诱导抗抑郁反应的能力,这种应激模型模拟了抑郁中发现的行为和神经化学改变,仍有待确定。因此,本研究调查了熊果酸在慢性不可预测应激(CUS)14 天的小鼠中可能具有的抗抑郁样作用,以及这种作用是否与调节血清皮质酮水平和海马 Bcl-2/Bax mRNA 表达有关。我们的结果表明,CUS 诱导了一种抑郁样行为,这表现在悬尾试验和浸水试验中,分别表现为不动时间和首次梳理潜伏期增加。相反,熊果酸(0.1mg/kg,po)或氟西汀(10mg/kg,po)在 CUS 的最后 7 天重复给药完全阻止了 CUS 诱导的行为改变,表明具有抗抑郁样作用。此外,CUS 显著增加了海马中 Bax(促凋亡标志物)的 mRNA 表达,但不增加 Bcl-2(抗凋亡标志物)的表达。此外,在 CUS 暴露的小鼠中检测到海马 Bcl-2/Bax 比值降低。熊果酸但不是氟西汀,阻止了 CUS 诱导的 Bax 表达增加,但熊果酸和氟西汀都阻止了 CUS 诱导的 Bcl-2/Bax 比值降低。此外,CUS 或用熊果酸或氟西汀治疗均未改变血清皮质酮水平。我们的研究揭示了熊果酸预防应激引起的抑郁样行为的能力,Bcl-2/Bax 表达的调节可能与这种反应有关。

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