School of Pharmacy, Anhui Provincial Laboratory of Inflammatory and Immunity Disease, Anhui Institute of Innovative Drugs, Anhui Medical University, Hefei, China.
School of Life Science, Anhui Agriculture University, Hefei, China.
Pharm Biol. 2022 Dec;60(1):1739-1750. doi: 10.1080/13880209.2022.2116460.
The traditional Chinese medicine formula Tao-Hong-Si-Wu decoction (TSD), used for treating ischaemic stroke, has the potential to treat depressive disorder (DD).
To explore the effective targets of TSD on DD animal models.
Sprague-Dawley (SD) rats were modelled by inducing chronic unpredictable mild stress (CUMS) during 35 days and treated with three dosages of TSD (2.5, 5 and 10 g/kg) or fluoxetine (10 mg/kg) by oral gavage for 14 days. Bodyweight measurements and behavioural tests were performed to observe the effect of TSD on the CUMS animals. A gas chromatography coupled with mass spectrometry (GC-MS)-based metabolomic analysis was conducted to reveal the metabolic characteristics related to the curative effect of TSD. Levels of the proteins associated with the feature metabolites were analysed.
Reduced immobile duration and crossed squares in the behavioural tests were raised by 48.6% and 32.9%, on average, respectively, by TSD treatment (ED=3.2 g/kg). Antidepressant effects of TSD were associated with 13 decreased metabolites and the restorations of ornithine and urea in the serum. TSD (5 g/kg) raised serum serotonin by 54.1 mg/dL but suppressed arginase I (Arg I) by 47.8 mg/dL in the CUMS rats. Proteins on the brain-derived neurotrophic factor (BDNF)-cAMP response element-binding protein (CREB) axis that modulate the inhibition of Arg I were suppressed in the CUMS rats but reversed by the TSD intervention.
TSD improves depression-like symptoms in CUMS rats. Further study will focus on the antidepressant-like effects of effective compounds contained in TSD.
用于治疗缺血性中风的中药方剂桃红四物汤(TSD)有可能治疗抑郁症(DD)。
探索 TSD 对 DD 动物模型的有效靶点。
通过在 35 天内诱导慢性不可预测轻度应激(CUMS)对 Sprague-Dawley(SD)大鼠进行建模,并通过口服灌胃用 TSD(2.5、5 和 10g/kg)或氟西汀(10mg/kg)治疗 14 天。进行体重测量和行为测试,观察 TSD 对 CUMS 动物的影响。进行基于气相色谱与质谱联用(GC-MS)的代谢组学分析,揭示与 TSD 疗效相关的代谢特征。分析与特征代谢物相关的蛋白质水平。
TSD 治疗平均使行为测试中的不动时间减少 48.6%,穿越方格数增加 32.9%(ED=3.2g/kg)。TSD 的抗抑郁作用与 13 种降低的代谢物有关,并恢复了血清中的鸟氨酸和尿素。TSD(5g/kg)使 CUMS 大鼠的血清 5-羟色胺升高 54.1mg/dL,但抑制了精氨酸酶 I(Arg I)47.8mg/dL。调节 Arg I 抑制的脑源性神经营养因子(BDNF)-cAMP 反应元件结合蛋白(CREB)轴上的蛋白质在 CUMS 大鼠中受到抑制,但 TSD 干预可逆转这种抑制。
TSD 改善了 CUMS 大鼠的抑郁样症状。进一步的研究将集中在 TSD 中有效化合物的抗抑郁样作用上。