Lang Jirui, Li Li, Quan Yunyun, Tan Ruirong, Zhao Jinbiao, Li Min, Zeng Jin, Chen Shilong, Wang Ting, Li Yong, Zhao Junning, Yin Zhujun
Biological Assay Key Laboratory of State Administration of Traditional Chinese Medicine for Traditional Chinese Medicine Quality, Translational Chinese Medicine Key Laboratory of Sichuan Province, Sichuan Engineering Technology Research Center of Genuine Regional Drug, Engineering Research Center for Formation Principle and Quality Evaluation of Genuine Medicinal Materials in Sichuan Province, Sichuan Academy of Chinese Medicine Sciences, Sichuan Institute for Translational Chinese Medicine, Chengdu, China.
Hunan Provincial Key Laboratory of the Research and Development of Novel Pharmaceutical Preparations, The "Double-First Class" Application Characteristic Discipline of Hunan Province (Pharmaceutical Science), Changsha Medical University, Changsha, China.
Front Pharmacol. 2023 Aug 11;14:1213602. doi: 10.3389/fphar.2023.1213602. eCollection 2023.
Wuwei Shexiang Pill (WSP) is a Tibetan traditional medicine, which has been demonstrated to exhibit potent anti-inflammatory and anti-gout effects. However, the specific pharmacological mechanism is not elucidated clearly. In the present study, liquid chromatography-mass spectrometry (LC-MS)-based metabolomics was applied to investigate the alteration of serum metabolites induced by WSP treatment in MSU-induced gouty rats. Subsequently, bioinformatics was utilized to analyze the potential metabolic pathway of the anti-gout effect of WSP. The pharmacodynamic data discovered that WSP could ameliorate ankle swelling and inflammatory cell infiltration, as well as downregulate the protein expression of IL-1β, p-NF-κB p65, and NLRP3 in the synovial membrane and surrounding tissues of gouty ankles. LC-MS-based metabolomics revealed that there were 30 differential metabolites in the serum between sham-operated rats and gouty ones, which were mainly involved in the metabolism of fructose and mannose, primary bile acid biosynthesis, and cholesterol metabolism. However, compared to the model group, WSP treatment upregulated 11 metabolic biomarkers and downregulated 31 biomarkers in the serum. KEGG enrichment analysis found that 27 metabolic pathways contributed to the therapeutic action of WSP, including linoleic acid metabolism, phenylalanine metabolism, and pantothenate and CoA biosynthesis. The comprehensive analysis-combined network pharmacology and metabolomics further revealed that the regulatory network of WSP against gout might be attributed to 11 metabolites, 7 metabolic pathways, 39 targets, and 49 active ingredients of WSP. In conclusion, WSP could ameliorate the inflammation of the ankle in MSU-induced gouty rats, and its anti-gout mechanism might be relevant to the modulation of multiple metabolic pathways, such as linoleic acid metabolism, phenylalanine metabolism, and pantothenate and CoA biosynthesis. This study provided data support for the secondary development of Chinese traditional patent medicine.
五味麝香丸(WSP)是一种藏药,已被证明具有强大的抗炎和抗痛风作用。然而,其具体的药理机制尚未完全阐明。在本研究中,采用基于液相色谱 - 质谱联用(LC - MS)的代谢组学方法,研究WSP对尿酸钠(MSU)诱导的痛风大鼠血清代谢物变化的影响。随后,利用生物信息学分析WSP抗痛风作用的潜在代谢途径。药效学数据表明,WSP可改善踝关节肿胀和炎症细胞浸润,并下调痛风性踝关节滑膜及周围组织中白细胞介素 - 1β、磷酸化核因子 - κB p65和NLRP3的蛋白表达。基于LC - MS的代谢组学研究发现,假手术大鼠和痛风大鼠血清中有30种差异代谢物,主要参与果糖和甘露糖代谢、初级胆汁酸生物合成以及胆固醇代谢。然而,与模型组相比,WSP治疗上调了血清中的11种代谢生物标志物,下调了31种生物标志物。京都基因与基因组百科全书(KEGG)富集分析发现,27条代谢途径对WSP的治疗作用有贡献,包括亚油酸代谢、苯丙氨酸代谢以及泛酸和辅酶A生物合成。综合网络药理学和代谢组学的分析进一步表明,WSP抗痛风的调控网络可能归因于WSP的11种代谢物、7条代谢途径、39个靶点和49种活性成分。总之,WSP可改善MSU诱导的痛风大鼠踝关节炎症,其抗痛风机制可能与多种代谢途径的调节有关,如亚油酸代谢、苯丙氨酸代谢以及泛酸和辅酶A生物合成。本研究为中药专利制剂的二次开发提供了数据支持。