Han Kaining, Feng Guangxin, Li Tanghao, Wan Zhili, Zhao Wenjing, Yang Xiaoquan
Laboratory of Food Proteins and Colloids, School of Food Science and Engineering, Guangdong Province Key Laboratory for Green Processing of Natural Products and Product Safety, South China University of Technology, Guangzhou, China.
School of Medicine, Shenzhen Campus of Sun Yat-sen University, Shenzhen, China.
Mol Nutr Food Res. 2023 Sep;67(17):e2200883. doi: 10.1002/mnfr.202200883. Epub 2023 Jul 9.
Soybean 7S globulin (β-conglycinin), a major soybean storage protein, has been demonstrated to exert remarkable triglyceride (TG) and cholesterol-lowering effects, yet the underlying mechanism remains controversial.
A comparative investigation is performed to assess the contribution of different structural domains of soybean 7S globulin, including core region (CR) and extension region (ER) domains, to biological effects of soybean 7S globulin using a high-fat diet rat model. The results show that ER domain mainly contributes to the serum TG-lowering effect of soybean 7S globulin, but not for CR domain. Metabolomics analysis reveals that oral administration of ER peptides obviously influences the metabolic profiling of serum bile acids (BAs), as well as significantly increased the fecal excretion of total BAs. Meanwhile, ER peptides supplementation reshapes the composition of gut microbiota and impacts the gut microbiota-dependent biotransformation of BAs which indicate by a significantly increased secondary BAs concentration in fecal samples. These results highlight that TG-lowering effects of ER peptides mainly stem from their modulation of BAs homeostasis.
Oral administration of ER peptides can effectively lower serum TG level by regulating BAs metabolism. ER peptides have potential to be used as a candidate pharmaceutical for the intervention of dyslipidemia.
大豆7S球蛋白(β-伴大豆球蛋白)是大豆的一种主要储存蛋白,已被证明具有显著的降低甘油三酯(TG)和胆固醇的作用,但其潜在机制仍存在争议。
采用高脂饮食大鼠模型,进行了一项比较研究,以评估大豆7S球蛋白不同结构域,包括核心区域(CR)和延伸区域(ER)结构域,对大豆7S球蛋白生物学效应的贡献。结果表明,ER结构域主要对大豆7S球蛋白的血清TG降低作用有贡献,而CR结构域则不然。代谢组学分析表明,口服ER肽明显影响血清胆汁酸(BAs)的代谢谱,同时显著增加粪便中总BAs的排泄。此外,补充ER肽可重塑肠道微生物群的组成,并影响肠道微生物群依赖的BAs生物转化,这表现为粪便样本中次级BAs浓度显著增加。这些结果表明,ER肽的TG降低作用主要源于其对BAs稳态的调节。
口服ER肽可通过调节BAs代谢有效降低血清TG水平。ER肽有潜力作为一种候选药物用于干预血脂异常。