4.5 Article

The effect of curculigo orchioides (Xianmao) on kidney energy metabolism and the related mechanism in rats based on metabolomics

Journal

FOOD SCIENCE & NUTRITION
Volume 9, Issue 11, Pages 6194-6212

Publisher

WILEY
DOI: 10.1002/fsn3.2573

Keywords

kidney energy metabolism; metabolomics; RT-PCR; Xianmao

Funding

  1. National Chinese Medicine Leading Talents Support Program-Qi Huang Scholars [[2018] 284]
  2. Jiangxi Provincial Technology Innovation Guidance Program [20192AEI91002]
  3. Jiangxi University of Traditional Chinese Medicine 1050 Youth Talent Project [5142001007]
  4. Key Technology for Safety Assessment of both Food and Traditional Chinese Medicine according to Tradition [2019YFC1604900]

Ask authors/readers for more resources

The study investigated the effects of Xianmao on kidney energy metabolism in rats, finding that Xianmao significantly increased enzyme activity and ATP content in the kidney, potentially mediated by various metabolic pathways and upregulation of specific genes.
The Chinese materia medica Xianmao (XM) is widely used in Chinese clinics and the traditional Chinese medicine diets. Although XM is often used to study its kidney-yang effect, the research on its effect on kidney energy metabolism and its mechanism is still relatively lacking. In this study, rats were given different doses of XM water extract for 4 weeks. Biochemical method was used to detect the content of serum biochemical indexes of liver and kidney function and blood lipid indicators, and HE staining method was used to observe the histopathological of liver and kidney in rats. The kidney Na+-K+-ATPase, Ca2+-Mg2+-ATPase, SDH (succinate dehydrogenase) enzyme activity, and the content of ATP in rats were measured. Metabolomics technology was used to analyze the potential biomarkers related to the effects of XM on kidney energy metabolism, and then, the metabolic pathways were analyzed. RT-PCR was used to detect the expression of Ampk, Sirt1, Ppar-alpha, and Pgc-1 alpha mRNA in kidney of rats. The results showed, compared with the blank control group, there was no significant effect on liver and kidney function in XMH, XMM, and XML groups. These significantly increased the kidney Na+-K+-ATPase, Ca2+-Mg2+-ATPase, SDH enzyme activity, and ATP content in XMH, XMM, and XML groups. Mitochondrial metabolic rate was inhibited in XMH group, but it was significantly increased in XMM and XML groups. The number of mitochondria was increased in XMH, XMM, and XML groups. Overall, these effects may be mediated by TCA cycle metabolism, butanoate metabolism, propanoate metabolism, alanine, aspartate, and glutamate metabolism, retinol metabolism, purine metabolism, pentose phosphate metabolism, aminoacyl-tRNA biosynthesis, valine, leucine, and isoleucine biosynthesis, and degradation metabolism pathways, as well as by increasing expression of upstream genes Ampk, Sirt1, Ppar-alpha, and Pgc-1 alpha mRNA.

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