The Beneficial Effects of Edible Kynurenic Acid from Marine Horseshoe Crab (Tachypleus tridentatus) on Obesity, Hyperlipidemia, and Gut Microbiota in High-Fat Diet-Fed Mice

Author:

Li Jian12,Zhang Yaqi1,Yang Shen12,Lu Zhenhua12,Li Guiling12,Wu Shangyi3,Wu Da-Ren12,Liu Jingwen1,Zhou Bo4,Wang Hui-Min David1567ORCID,Huang Shi-Ying12ORCID

Affiliation:

1. College of Food and Biological Engineering, Jimei University, Xiamen 361021, China

2. Fujian Provincial Engineering Technology Research Center of Marine Functional Food, Xiamen 361021, China

3. Xiamen Bioendo Technology Co., Ltd., Xiamen 361022, China

4. Department of Microbiology, College of Life Sciences, Shandong Agricultural University, Tai’an 271018, China

5. Graduate Institute of Biomedical Engineering, National Chung Hsing University, Taichung 402, Taiwan

6. Graduate Institute of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan

7. Department of Medical Laboratory Science and Biotechnology, China Medical University, Taichung 404, Taiwan

Abstract

The marine horseshoe crab (Tachypleus tridentatus) has been considered as food and traditional medicine for many years. Kynurenic acid (KA) was isolated from horseshoe crab in this study for the first time in the world. A previous study in 2018 reported that intraperitoneal administration of KA prevented high-fat diet- (HFD-) induced body weight gain. Now, we investigated the effects of intragastric gavage of KA on HFD mice and found that KA (5 mg/kg/day) inhibited both the body weight gain and the increase of average daily energy intake. KA reduced serum triglyceride and increased serum high-density lipoprotein cholesterol. KA inhibited HFD-induced the increases of serum low-density lipoprotein cholesterol, coronary artery risk index, and atherosclerosis index. KA also suppressed HFD-induced the increase of the ratio of Firmicutes to Bacteroidetes (two dominant gut microbial phyla). KA partially reversed HFD-induced the changes in the composition of gut microbial genera. These overall effects of KA on HFD mice were similar to that of simvastatin (positive control). But the effects of 1.25 mg/kg/day KA on HFD-caused hyperlipidemia were similar to the effects of 5 mg/kg/day simvastatin. The pattern of relative abundance in 40 key genera of gut microbiota from KA group was closer to that from the normal group than that from the simvastatin group. In addition, our in vitro results showed the potential antioxidant activity of KA, which suggests that the improvement effects of KA on HFD mice may be partially associated with antioxidant activity of KA. Our findings demonstrate the potential role of KA as a functional food ingredient for the treatment of obesity and hyperlipidemia as well as the modulation of gut microbiota.

Funder

Jimei University Research Foundation

Publisher

Hindawi Limited

Subject

Cell Biology,Ageing,General Medicine,Biochemistry

Reference60 articles.

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