Tao-Hong-Si-Wu decoction improves depressive symptoms in model rats via amelioration of BDNF-CREB-arginase I axis disorders

Pharm Biol. 2022 Dec;60(1):1739-1750. doi: 10.1080/13880209.2022.2116460.

Abstract

Context: The traditional Chinese medicine formula Tao-Hong-Si-Wu decoction (TSD), used for treating ischaemic stroke, has the potential to treat depressive disorder (DD).

Objective: To explore the effective targets of TSD on DD animal models.

Materials and methods: 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.

Results: Reduced immobile duration and crossed squares in the behavioural tests were raised by 48.6% and 32.9%, on average, respectively, by TSD treatment (ED50=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.

Discussion and conclusions: TSD improves depression-like symptoms in CUMS rats. Further study will focus on the antidepressant-like effects of effective compounds contained in TSD.

Keywords: GC–MS; Metabolomics; depressive disorder; traditional Chinese medicine.

MeSH terms

  • Animals
  • Antidepressive Agents / pharmacology
  • Arginase / metabolism
  • Arginase / pharmacology
  • Brain Ischemia*
  • Brain-Derived Neurotrophic Factor / metabolism
  • Cyclic AMP Response Element-Binding Protein / metabolism
  • Depression / drug therapy
  • Depression / metabolism
  • Drugs, Chinese Herbal
  • Hippocampus
  • Rats
  • Rats, Sprague-Dawley
  • Stress, Psychological / drug therapy
  • Stress, Psychological / metabolism
  • Stroke*

Substances

  • Antidepressive Agents
  • Brain-Derived Neurotrophic Factor
  • Cyclic AMP Response Element-Binding Protein
  • Drugs, Chinese Herbal
  • si-wu decoction
  • Arginase

Grants and funding

The study is supported by the National Natural Science Foundation of China (0601055205), Anhui Natural Science Foundation (2008085QH364) and Anhui Medical University (XJ201729, 2020xkjT019, and 2021lcxk026).