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Exploration of the main active components and pharmacological mechanism of Yerba Mate based on network pharmacology.
Yue, Zhaodi; Fu, Hui; Ma, Huifen; Ma, Huifen; Li, Li; Feng, Ziyun; Yin, Yanyan; Wang, Fangqi; Du, Bingyu; Liu, Yibo; Zhao, Renjie; Kan, Mengfan; Sun, Helin; Zhang, Zhongwen; Yu, Shaohong.
Affiliation
  • Yue Z; Department of Rehabilitation Medicine, Department of Endocrinology and Metabology, Shandong University of Traditional Chinese Medicine, The Second Affiliated Hospital of Shandong University of Traditional Chinese Medicine, The First Affiliated Hospital of Shandong First Medical University & Shan
  • Fu H; Department of Endocrinology and Metabology, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Shandong Key Laboratory of Rheumatic Disease and Translational medicine, Shandong Institute of Nephrology, Jinan, China.
  • Ma H; College of Rehabilitation Medicine, Shandong University of Traditional Chinese Medicine, Jinan, China.
  • Ma H; Cheeloo College of Medicine, Shandong University, Jinan, China.
  • Yin Y; Department of Rehabilitation Medicine, Department of Endocrinology and Metabology, Shandong University of Traditional Chinese Medicine, The Second Affiliated Hospital of Shandong University of Traditional Chinese Medicine, The First Affiliated Hospital of Shandong First Medical University & Shan
  • Wang F; Department of Rehabilitation Medicine, Department of Endocrinology and Metabology, Shandong University of Traditional Chinese Medicine, The Second Affiliated Hospital of Shandong University of Traditional Chinese Medicine, The First Affiliated Hospital of Shandong First Medical University & Shan
  • Du B; Department of Rehabilitation Medicine, Department of Endocrinology and Metabology, Shandong University of Traditional Chinese Medicine, The Second Affiliated Hospital of Shandong University of Traditional Chinese Medicine, The First Affiliated Hospital of Shandong First Medical University & Shan
  • Liu Y; Department of Endocrinology and Metabology, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Shandong Key Laboratory of Rheumatic Disease and Translational medicine, Shandong Institute of Nephrology, Jinan, China.
  • Zhao R; College of Rehabilitation Medicine, Shandong University of Traditional Chinese Medicine, Jinan, China.
  • Kan M; College of Rehabilitation Medicine, Shandong University of Traditional Chinese Medicine, Jinan, China.
  • Sun H; Department of Rehabilitation Medicine, Department of Endocrinology and Metabology, Shandong University of Traditional Chinese Medicine, The Second Affiliated Hospital of Shandong University of Traditional Chinese Medicine, The First Affiliated Hospital of Shandong First Medical University & Shan
  • Zhang Z; Department of Endocrinology and Metabology, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Shandong Key Laboratory of Rheumatic Disease and Translational medicine, Shandong Institute of Nephrology, Jinan, China.
  • Yu S; College of Rehabilitation Medicine, Shandong University of Traditional Chinese Medicine, Jinan, China.
Endokrynol Pol ; 73(4): 725-735, 2022.
Article in En | MEDLINE | ID: mdl-36059165
ABSTRACT

INTRODUCTION:

Yerba mate is widely consumed in South American countries and is gaining popularity around the world. Long-term consumption of yerba mate has been proven to have health-care functions and therapeutic effects on many diseases; however, its underlying mechanism has not been clearly elucidated. In this research, we explored the pharmacological mechanism of yerba mate through a network pharmacological approach. MATERIAL AND

METHODS:

The bioactive components of yerba mate were screened from published literature and the Traditional Chinese Medicine System Pharmacology Database (TCMSP), and the targets and related diseases were retrieved by TCMSP. Furthermore, the component-target-disease network an protein-protein interaction (PPI) network were constructed, and combined with gene ontology (GO) functional analysis and Kyoto Encyclopaedia of Genes and Genomes (KEGG) pathway enrichment analysis to explore the pharmacological mechanism of yerba mate.

RESULTS:

As a result, 16 bioactive components of yerba mate were identified, which acted on 229 targets in total. Yerba mate can be used to treat 305 diseases, such as breast cancer, asthma, Alzheimer's disease, osteoarthritis, diabetes mellitus, atherosclerosis, and obesity. Protein kinase B (AKT1), signal transducer and activator of transcription 3 (STAT3), mitogen-activated protein kinase 1 (MAPK1), transcription factor AP-1 (JUN), cellular tumour antigen (p53) TP53, tumour necrosis factor (TNF), transcription factor p65 (RELA), interleukin-6 (IL6), amyloid-beta precursor protein (APP), and vascular endothelial growth factor A (VEGFA) were identified as the key targets of yerba mate playing pharmacological roles. The signalling pathways identified by KEGG pathway enrichment analysis that were most closely related to the effects of yerba mate included pathways in cancer, fluid shear stress and atherosclerosis, and human cytomegalovirus infection.

CONCLUSION:

the results of our study preliminarily verify the basic pharmacological action and possible mechanism of yerba mate and provide a reference for the further development of its medicinal value.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ilex paraguariensis / Atherosclerosis / Neoplasms Type of study: Prognostic_studies Limits: Humans Language: En Journal: Endokrynol Pol Year: 2022 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ilex paraguariensis / Atherosclerosis / Neoplasms Type of study: Prognostic_studies Limits: Humans Language: En Journal: Endokrynol Pol Year: 2022 Document type: Article
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