4.7 Article

Anti-NAFLD effect of defatted walnut powder extract in high fat diet-induced C57BL/6 mice by modulating the gut microbiota

Journal

JOURNAL OF ETHNOPHARMACOLOGY
Volume 270, Issue -, Pages -

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.jep.2021.113814

Keywords

Defatted walnut powder extract; NAFLD; Pseudo-sterile mice; Oxidative stress; Gut microbiota; HPLC-Q-TOF/MS

Funding

  1. National Natural Science Foundation of China [81470176, 81773879]
  2. Overseas Training Project of Liaoning Colleges and Universities [2018LNGXGJWPY-YB024]
  3. fourth national investigation of Chinese materia medica resources in Liaoning Province [2018017, 2019019]

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DWPE has a preventive effect on NAFLD, which may be related to the regulation of gut microbiota. The oral administration of DWPE can alleviate hepatic lipid accumulation and reduce inflammation markers. Antibiotics treatment diminishes the efficacy of DWPE, suggesting the importance of gut microbiota in the therapeutic process.
Ethnopharmacological relevance: Walnut kernel has the actions of removing meteorism, dissipating stagnation and removing blood stasis and is used after being defatted in TCM. Defatted walnut powder extract (DWPE) has the abilities of anti-oxidation and lowering lipid levels in vivo. However, the effects and the potential mechanisms of DWPE on NAFLD have not been explored. Aim of the study: The study were to investigate the anti-NAFLD effect of DWPE in high fat diet-induced C57BL/6 mice and demonstrate that whether DWPE developed the effect on anti-NAFLD by remodeling the compositions and abundances of gut microbiota. Materials and methods: The inhibitory effect of DWPE on the development of NAFLD was conducted on C57BL/6 mice with a high fat diet and the regulation effect of DWPE on gut microbiota was verified on pseudo-sterile mice with treatment of broad spectrum antibiotics. Results: The results showed that the oral administration of DWPE remarkably alleviated hepatic lipid accumulation by decreasing the levels of TG, TC, LDL, MDA and increasing HDL. Meanwhile, the expressions of NF-kappa B and MAPKs family proteins were reduced by DWPE compared with HFD group. Otherwise, the efficacy of anti-NAFLD of DWPE was significantly decreased after treatment of antibiotics, which indicated the key role of gut microbiota in the therapeutic process. Furthermore, sequencing of 16S rRNA gene revealed that DWPE could revert the decreased relative abundance of gut microbiota caused by the long term of a high fat diet. And the disordered microflora was remodeled by DWPE including the reduction of Erysipelotrichia, Firmicutes and Actinobacteria as well as the increment of Bacteroidetes, Clostridiales, Bacteroidales S24-7, Prevotellaceae and Bacteroides. Conclusion: Taken together, DWPE had a preventing effect on NAFLD, which might be associated with the regulation of gut microbiota.

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