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Dynamic changes in marker components during the stir-frying of Pharbitidis Semen, and network analysis of its potential effects on nephritis

Affiliation
Jiangsu Key Laboratory of Marine Bioresources and Environment ,Jiangsu Ocean University ,Lianyungang ,China
Li, Yuman;
Affiliation
Jiangsu Key Laboratory of Marine Bioresources and Environment ,Jiangsu Ocean University ,Lianyungang ,China
Lu, Yuhe;
Affiliation
Jiangsu Key Laboratory of Marine Bioresources and Environment ,Jiangsu Ocean University ,Lianyungang ,China
Zhu, Yujie;
Affiliation
Lunan Pharmaceutical Group Limited by Share Ltd ,Linyi ,China
Yao, Jingchun;
Affiliation
Jiangyin Hospital Affiliated to Nanjing University of Chinese Medicine ,Wuxi ,China
Hua, Haibing;
Affiliation
Jiangsu Key Laboratory of Marine Bioresources and Environment ,Jiangsu Ocean University ,Lianyungang ,China
Shen, Jinyang;
Affiliation
Jiangsu Key Laboratory of Marine Bioresources and Environment ,Jiangsu Ocean University ,Lianyungang ,China
Gao, Xun;
Affiliation
Jiangsu Key Laboratory of Marine Bioresources and Environment ,Jiangsu Ocean University ,Lianyungang ,China
Qin, Kunming

Introduction: Pharbitidis Semen (PS) has been widely used in traditional Chinese medicine to treat several diseases such as nephritis. PS is usually stir-fried to enhance its therapeutic efficacy before use in clinical practice. However, the changes in phenolic acids during stir-frying and the mechanisms of their therapeutic effects on nephritis are still unclear. Methods: Here, we studied the processing-induced chemical changes and elucidated the mechanism of PS in the treatment of nephritis. We determined the levels of the 7 phenolic acids in raw PS (RPS) and stir-fried PS (SPS) using high-performance liquid chromatography, analyzed the dynamic compositional changes during stir-frying, and used network analysis and molecular docking to predict and verify compound targets and pathways corresponding to nephritis. Results: The dynamic changes in the 7 phenolic acids in PS during stir-frying are suggestive of a transesterification reaction. Pathway analysis revealed that the targets of nephritis were mainly enriched in the AGE-RAGE, hypoxia-inducible factor-1, interleukin-17, and tumor necrosis factor signaling pathways among others. Molecular docking results showed that the 7 phenolic acids had good binding ability with the key nephritic targets. Discussion: The potential pharmaceutical basis, targets, and mechanisms of PS in treating nephritis were explored. Our findings provide a scientific basis for the clinical use of PS in treating nephritis.

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License Holder: Copyright © 2023 Li, Lu, Zhu, Yao, Hua, Shen, Gao and Qin.

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