College of Veterinary Medicine, Jilin University, Changchun 130062, China.
J Agric Food Chem. 2022 Aug 31;70(34):10620-10634. doi: 10.1021/acs.jafc.2c04476. Epub 2022 Aug 16.
Nonalcoholic fatty liver disease (NAFLD) is among the most prevalent chronic liver diseases around the globe. The accumulation of lipids in the liver and oxidative stress are important pathological mechanisms of NAFLD. Astaxanthin (AT) is a carotenoid extracted from shrimps and crabs with beneficial biological activities, including anti-oxidative and anti-inflammatory activities. 16S microflora sequencing, H&E staining, and the western blot technique were employed to investigate the impacts of AT on a high-fat diet (HFD)-induced NAFLD. Significant mitigation in lipid metabolism-related disorders and decreased oxidative stress in HFD-induced mice were observed due to AT, and significant changes in the gut flora of the model mice were also observed. The study showed that AT considerably lowered the protein expression level of fatty acid synthetase (FAS), sterol regulatory element-binding protein-1c (SREBP-1c), and acetyl-COA carboxylase (ACC) and increased the protein expression of nuclear factor-E2 associated factor 2 (Nrf2) and AMP-activated protein kinase (AMPK) in oleic acid (OA) and palmitic acid (PA)-induced HepG2 cells. Additionally, mechanistic studies revealed that compound C (AMPK inhibitor, CC) inhibited the regulatory effect of AT on the SREBP-1c and Nrf2 signaling pathways. In conclusion, AT can inhibit the SREBP-1c, FAS, and ACC signaling pathways, activate the AMPK and Nrf2 signaling pathways, and improve the structure of intestinal flora.
非酒精性脂肪性肝病 (NAFLD) 是全球最常见的慢性肝病之一。肝脏中脂质的积累和氧化应激是非酒精性脂肪性肝病的重要病理机制。虾青素 (AT) 是一种从虾和蟹中提取的类胡萝卜素,具有有益的生物活性,包括抗氧化和抗炎活性。16S 微生物测序、H&E 染色和 Western blot 技术用于研究 AT 对高脂肪饮食 (HFD) 诱导的 NAFLD 的影响。由于 AT,HFD 诱导的小鼠的脂质代谢相关紊乱得到显著缓解,氧化应激降低,模型小鼠的肠道菌群也发生了显著变化。研究表明,AT 可显著降低油酸 (OA) 和棕榈酸 (PA) 诱导的 HepG2 细胞中脂肪酸合成酶 (FAS)、固醇调节元件结合蛋白-1c (SREBP-1c) 和乙酰辅酶 A 羧化酶 (ACC) 的蛋白表达水平,并增加核因子-E2 相关因子 2 (Nrf2) 和 AMP 激活蛋白激酶 (AMPK) 的蛋白表达。此外,机制研究表明,化合物 C (AMPK 抑制剂,CC) 抑制了 AT 对 SREBP-1c 和 Nrf2 信号通路的调节作用。总之,AT 可抑制 SREBP-1c、FAS 和 ACC 信号通路,激活 AMPK 和 Nrf2 信号通路,改善肠道菌群结构。