Mechanisms of radix rehmanniae praeparata in treating blood deficiency: A study on chemistry, metabolomics, and gut microbiota

To investigate the mechanism of Radix Rehmanniae Praeparata (RRP) in treating blood deficiency syndrome (BDS) by analyzing the changes in chemical components before and after processing, and its effects on metabolomics and gut microbiota in BDS mice. Ultra-high-performance liquid chromatographyquadrupole time-of-flight mass spectrometry (UPLC-Q-TOF-MS) was employed to screen differential components before and after the processing of Radix Rehmanniae (RR). Pharmacodynamic studies were conducted to validate the therapeutic effects. Additionally, UPLC-Q-TOF-MS, headspace sampling-gas chromatography-mass spectrometry (HS-GC-MS), and 16sRNA sequencing were used to investigate the regulatory effects of RRP on metabolomics and the gut microbiota in BDS mice. The primary differential components identified were iridoids, phenylethanoid glycosides, sugars, benzaldehydes, and 5-hydroxymethylfurfural and its derivatives. RRP effectively ameliorated blood and energy metabolism in BDS mice. It regulates the biosynthesis pathway of unsaturated fatty acids, increases the abundance of Firmicutes to elevate butyric acid levels, and reduces the abundance of Bacteroidetes to downregulate acetic and propionic acid levels, thereby exerting therapeutic effects on BDS. RRP attenuated the metabolic state of BDS mice by modulating metabolic pathways and gut microbiota balance, providing a scientific basis for its clinical application.

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Publication Details

Journal
Chinese Journal of Analytical Chemistry
Published
2025-04-17
DOI
https://doi.org/10.1016/j.cjac.2025.100548
Citations
2
Primary Topic
Metabolomics and Mass Spectrometry Studies
Type
article
Field-Weighted Citation Impact
1.61

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article

Mechanisms of radix rehmanniae praeparata in treating blood deficiency: A study on chemistry, metabolomics, and gut microbiota

Xuwen Liu, Runping Gao, Guoshun Shan, F Wang et al.
2 citations
Chinese Journal of Analytical Chemistry
Metabolomics and Mass Spectrometry Studies
1.61
article

Mechanisms of radix rehmanniae praeparata in treating blood deficiency: A study on chemistry, metabolomics, and gut microbiota

Xuwen Liu, Runping Gao, Guoshun Shan, F Wang, Chengwei Ulrika Yuan
article en
2 citations

Abstract

To investigate the mechanism of Radix Rehmanniae Praeparata (RRP) in treating blood deficiency syndrome (BDS) by analyzing the changes in chemical components before and after processing, and its effects on metabolomics and gut microbiota in BDS mice. Ultra-high-performance liquid chromatographyquadrupole time-of-flight mass spectrometry (UPLC-Q-TOF-MS) was employed to screen differential components before and after the processing of Radix Rehmanniae (RR). Pharmacodynamic studies were conducted to validate the therapeutic effects. Additionally, UPLC-Q-TOF-MS, headspace sampling-gas chromatography-mass spectrometry (HS-GC-MS), and 16sRNA sequencing were used to investigate the regulatory effects of RRP on metabolomics and the gut microbiota in BDS mice. The primary differential components identified were iridoids, phenylethanoid glycosides, sugars, benzaldehydes, and 5-hydroxymethylfurfural and its derivatives. RRP effectively ameliorated blood and energy metabolism in BDS mice. It regulates the biosynthesis pathway of unsaturated fatty acids, increases the abundance of Firmicutes to elevate butyric acid levels, and reduces the abundance of Bacteroidetes to downregulate acetic and propionic acid levels, thereby exerting therapeutic effects on BDS. RRP attenuated the metabolic state of BDS mice by modulating metabolic pathways and gut microbiota balance, providing a scientific basis for its clinical application.

Chinese Journal of Analytical ChemistryVol. 53(7)
Liaoning University of Traditional Chinese Medicine (CN)
Department of Education of Liaoning Province, Liaoning University of Traditional Chinese Medicine, Department of Science and Technology of Liaoning Province
Zero hunger
Openalex Percentile: Top 18%
Metabolomics and Mass Spectrometry Studies
1.61
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