Gong Yulong, Xi Longwei, Liu Yulong, Lu Qisheng, Zhang Zhimin, Liu Haokun, Jin Junyan, Yang Yunxia, Zhu Xiaoming, Xie Shouqi, Han Dong
State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China.
College of Advanced Agricultural Sciences, University of Chinese Academy of Sciences, Beijing 100049, China.
Aquac Nutr. 2023 Jul 20;2023:6672985. doi: 10.1155/2023/6672985. eCollection 2023.
The present study investigated the sequential regulation signals of high-carbohydrate diet (HCD)-induced hepatic lipid deposition in gibel carp (). Two isonitrogenous and isolipidic diets, containing 25% (normal carbohydrate diet, NCD) and 45% (HCD) corn starch, were formulated to feed gibel carp (14.82 ± 0.04 g) for 8 weeks. The experimental fish were sampled at 2, 4, 6, and 8 week. In HCD group, the hyperlipidemia and significant hepatic lipid deposition (oil red O area and triglyceride content) was found at 4, 6, and 8 week, while the significant hyperglycemia was found at 2, 4, and 8 week, compared to NCD group ( < 0.05). HCD induced hepatic lipid deposition via increased hepatic lipogenesis (, , and ) but not decreased hepatic lipolysis ( and ). When compared with NCD group, HCD significantly elevated the hepatic sterol regulatory element binding proteins 1 (SREBP1) signals (positive hepatocytes and fluorescence intensity) at 4, 6, and 8 week ( < 0.05). The hepatic SREBP1 signals increased from 2 to 6 week, but decreased at 8 week due to substantiated insulin resistance (plasma insulin levels, plasma glucose levels, and P-AKT levels) in HCD group. Importantly, the hepatic carbohydrate response element binding protein (ChREBP) signals (positive hepatocytes, fluorescence intensity, and expression levels) were all significantly elevated by HCD-induced glucose-6-phosphate (G6P) accumulation at 2, 4, 6, and 8 week ( < 0.05). Compared to 2 and 4 week, the hepatic ChREBP signals and G6P contents was significantly increased by HCD at 6 and 8 week ( < 0.05). The HCD-induced G6P accumulation was caused by the significantly increased expression of hepatic , , and ( < 0.05) but not at 4, 6, and 8 week, compared to NCD group. These results suggested that the HCD-induced hepatic lipid deposition was mainly promoted by SREBP1 in earlier stage and by ChREBP in later stage for gibel carp. This study revealed the sequential regulation pathways of the conversion from feed carbohydrate to body lipid in fish.
本研究调查了高碳水化合物饮食(HCD)诱导银鲫肝脏脂质沉积的顺序调节信号。配制了两种等氮等脂饮食,分别含有25%(正常碳水化合物饮食,NCD)和45%(HCD)的玉米淀粉,用于投喂银鲫(14.82±0.04克)8周。在第2、4、6和8周对实验鱼进行采样。与NCD组相比,在HCD组中,4、6和8周时出现高脂血症和显著的肝脏脂质沉积(油红O面积和甘油三酯含量),而在2、4和8周时出现显著的高血糖(P<0.05)。HCD通过增加肝脏脂肪生成(脂肪酸合酶、乙酰辅酶A羧化酶和固醇调节元件结合蛋白1)诱导肝脏脂质沉积,但不通过减少肝脏脂肪分解(激素敏感性脂肪酶和肉碱棕榈酰转移酶1)。与NCD组相比,HCD在4、6和8周时显著提高了肝脏固醇调节元件结合蛋白1(SREBP1)信号(阳性肝细胞和荧光强度)(P<0.05)。HCD组肝脏SREBP1信号在2至6周增加,但在8周时由于证实的胰岛素抵抗(血浆胰岛素水平、血浆葡萄糖水平和磷酸化AKT水平)而下降。重要的是,在2、4、6和8周时,HCD诱导的葡萄糖-6-磷酸(G6P)积累使肝脏碳水化合物反应元件结合蛋白(ChREBP)信号(阳性肝细胞、荧光强度和表达水平)均显著升高(P<0.05)。与2和4周相比,HCD在6和8周时显著增加了肝脏ChREBP信号和G6P含量(P<0.05)。与NCD组相比,在4、6和8周时,HCD诱导的G6P积累是由肝脏葡萄糖激酶、磷酸果糖激酶1和葡萄糖-6-磷酸酶表达显著增加引起的,而不是由葡萄糖-6-磷酸脱氢酶引起的。这些结果表明,对于银鲫,HCD诱导的肝脏脂质沉积在早期主要由SREBP1促进,在后期由ChREBP促进。本研究揭示了鱼类从饲料碳水化合物转化为体脂的顺序调节途径。