4.7 Article

Sacha Inchi Oil Press-Cake Protein Hydrolysates Exhibit Anti-Hyperuricemic Activity via Attenuating Renal Damage and Regulating Gut Microbiota

Journal

FOODS
Volume 11, Issue 16, Pages -

Publisher

MDPI
DOI: 10.3390/foods11162534

Keywords

sacha inchi oil press-cake protein hydrolyzates; hyperuricemia; renal injury; gut microbiota

Funding

  1. China Agriculture Research System of MOF and MARA [CARS-21]
  2. Natural Science Foundation of Guangdong Province [2020A1515011268]
  3. Key Area Research and Development Program of Guangdong Province [2020B020226008]
  4. Du Bing Expert Workstation Project of Yunnan Province [202005AF150071]

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The protein hydrolysates of sacha inchi oil press-cake (SISH) were found to have anti-hyperuricemic effects by regulating gene expression and inhibiting uric acid synthesis enzyme activity. Additionally, SISH reduced renal damage, suppressed inflammation-related gene expression, and improved gut microbiota dysbiosis.
The incidence of hyperuricemia has increased globally due to changes in dietary habits. The sacha inchi oil press-cake is generally discarded, resulting in the waste of resources and adverse environmental impact. For the purpose of developing sacha inchi oil press-cake and identifying natural components with anti-hyperuricemic activities, we systemically investigated the underlying mechanisms of sacha inchi oil press-cake protein hydrolysates (SISH) in the hyperuricemic rat model. SISH was obtained from sacha inchi oil press-cake proteins after trypsin treatment, and 24 peptides with small molecular weight (<1000 Da) were identified. The results of animal experiments showed that SISH significantly decreased the serum uric acid (UA) level by inhibiting the xanthine oxidase (XOD) activity and regulating the gene expression related to UA production and catabolism in hyperuricemia rats, such as Xdh and Hsh. In addition, SISH attenuated the renal damage and reduced the gene expression related to inflammation (Tlr4, Map3k8, Pik3cg, Pik3ap1, Ikbke, and Nlrp3), especially Tlr4, which has been considered a receptor of UA. Notably, SISH reversed high purine-induced gut microbiota dysbiosis, particularly by enhancing the relative abundance of butyric acid-producing bacteria (unidentified_Ruminococcaceae, Oscillibacter, , Ruminiclostridium, Intestinimonas). This research provided new insights into the treatment of hyperuricemia.

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