Wang Jing-Hua, Hwang Seung-Ju, Shin Kwang-Soo, Lim Dong-Woo, Son Chang-Gue
Institute of Bioscience & Integrative Medicine, Daejeon University, 75, Daedeok-daero 176, Seo-gu, Daejeon 35235, Republic of Korea.
Liver and Immunology Research Center, Daejeon Korean Medicine Hospital, 75, Daedeok-daero 176, Seo-gu, Daejeon 35235, Republic of Korea.
Antioxidants (Basel). 2022 Nov 15;11(11):2254. doi: 10.3390/antiox11112254.
In modern society, numerous metabolic disorders are widespread globally. The present study aimed to demonstrate whether -fermented (BSAX) exerts anti-metabolic disturbance effects compared with the ethyl acetate fraction of (EFAX), a previously verified functional fraction. Mice fed with a high-fat, high-fructose diet (HFHFD) for 10 wk presented a typical model of metabolic dysfunction, and BSAX significantly attenuated a string of metabolic-syndrome-related pathological parameters, such as body, fat, organ mass, lipid markers (TGs, TC, free fatty acids), and glucose metabolism (glucose, insulin), without influencing appetite. Further, BSAX markedly lowered malondialdehyde (MDA) and ROS in the blood and restored antioxidative parameters (SOD, GSH, and CAT in liver tissue, and total bilirubin in serum) by elevating Nrf2 and HO-1. Moreover, BSAX noticeably restored gut microbiota diversity and normalized lipid-metabolism-associated proteins, including SREBP-1, p-AMPK, and PPAR-α. Generally, most metabolic parameters were improved by BSAX to a greater extent than EFAX, except for liver weight and hepatic TC. In conclusion, BSAX alleviates metabolic dysfunction by enhancing lipid metabolism and antioxidative capacity and is more effective than EFAX. Therefore, the application of high-yield, effective BSAX might be a promising approach for curing and preventing metabolic disorders.
在现代社会,众多代谢紊乱在全球广泛存在。本研究旨在证明与已被证实具有功能活性的乙酸乙酯提取物(EFAX)相比,-发酵提取物(BSAX)是否具有抗代谢紊乱作用。用高脂高果糖饮食(HFHFD)喂养10周的小鼠呈现出典型的代谢功能障碍模型,BSAX显著减轻了一系列与代谢综合征相关的病理参数,如体重、脂肪、器官质量、脂质标志物(甘油三酯、总胆固醇、游离脂肪酸)和葡萄糖代谢(葡萄糖、胰岛素),且不影响食欲。此外,BSAX显著降低血液中的丙二醛(MDA)和活性氧(ROS),并通过提高核因子E2相关因子2(Nrf2)和血红素加氧酶-1(HO-1)来恢复抗氧化参数(肝组织中的超氧化物歧化酶、谷胱甘肽和过氧化氢酶,以及血清中的总胆红素)。此外,BSAX显著恢复肠道微生物群多样性,并使与脂质代谢相关的蛋白质正常化,包括固醇调节元件结合蛋白-1(SREBP-1)、磷酸化的腺苷酸活化蛋白激酶(p-AMPK)和过氧化物酶体增殖物激活受体-α(PPAR-α)。总体而言,除肝脏重量和肝脏总胆固醇外,BSAX对大多数代谢参数的改善程度均大于EFAX。总之,BSAX通过增强脂质代谢和抗氧化能力来减轻代谢功能障碍,且比EFAX更有效。因此,应用高产、有效的BSAX可能是治疗和预防代谢紊乱的一种有前景的方法。