饥饿及再投喂处理对草鱼生长、葡萄糖代谢和转运蛋白1表达的影响
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广东海洋大学 水产动物营养与饲料实验室, 广东 湛江 524088

作者简介:

李锐鑫(1993-),男,硕士研究生,主要从事水产动物营养学研究.E-mail:270079895@qq.com

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S963

基金项目:

国家自然科学基金项目(31272673);国家973重点基础研究计划项目(2014CB138603);广东省珠江学者基金项目(GDUPS2011);广东省自然科学基金项目(S2013010016511);湛江市科技攻关项目(2016A03011).


Effects of starvation and refeeding on growth performance, glucose metabolism, and expression of glucose transporter 1 in Ctenopharyngodon idellus
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Laboratory of Aquatic Animal Nutrition and Feed, Fisheries College, Guangdong Ocean University, Zhanjiang 524088, China

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    摘要:

    设置持续投喂组(C,持续投喂8周)、饥饿再投喂组(R,饥饿4周+再投喂4周)和持续饥饿组(S,饥饿8周)3个处理组,研究3种不同饥饿处理对草鱼()血清生化指标、糖原和糖代谢相关酶和葡萄糖转运蛋白1(GLUT1)的影响,同时在此实验基础上研究草鱼在急性高糖负荷胁迫下的糖耐受能力、糖代谢相关酶和GLUT1的变化规律,旨在阐明草鱼在饥饿及再投喂处理条件下的糖代谢特征。选取初重为(125.35±0.54)g的草鱼,饲养8周后以30 mg/100 g体重的剂量腹腔注射葡萄糖研究其糖耐受能力。结果显示,S组肝糖原和血清的血糖、甘油三酯含量均最低。饥饿处理对草鱼糖耐受能力影响显著,S组血糖含量在各时间点上显著低于其余两组(<0.05),肝糖原在6 h达到峰值;饥饿处理对草鱼肝脏糖代谢关键酶影响显著,饥饿处理(S组)诱使磷酸烯醇式丙酮酸激酶(PEPCK)活性上升但抑制丙酮酸激酶(PK)和果糖-6-磷酸激酶(PFK)的活性(<0.05),而饥饿再投喂(R组)后PEPCK、PK和PFK酶活性恢复到持续投喂(C组)处理水平。注射葡萄糖后S组肝脏GK酶活性增幅最大,PK酶活性呈上升趋势,而R组则呈先下降后上升的趋势;饥饿处理对草鱼肝脏和肌肉GLUT1表达量在各个时间点上均高于其余两组(<0.05)。研究结果表明,在不同饥饿处理下,草鱼可通过消耗肝糖原和甘油三酯及降低肝脏糖酵解相关酶(PK和PFK)活性和促进糖异生PEPCK酶活性来应对饥饿胁迫,而饥饿处理可诱使GK和PK酶活性上升、促进糖原合成和激活基因的表达和转运来缓解草鱼急性高糖负荷,从而提高其糖耐受能力。

    Abstract:

    This experiment was conducted to determine the effects of starvation and refeeding on the growth performance, biochemical indices in the plasma, liver/muscle glycogen content, glucose metabolic enzymes, and gene expression of glucose transporter 1 () and then clarify the characteristics of glucose metabolism of grass carp under starvation and refeeding. The combined experiment consisted of a starvation group (S), refeeding group (R, starvation 4 weeks + refeeding 4 weeks), and continuous feeding group (C). Fish with an average initial weight of (125.35±0.54) g were randomly selected in each treatment and injected with 300 mg glucose per 100 g body weight for a glucose tolerance test (GTT) at the end of experiment. The results showed that starvation resulted in a low liver glycogen content, plasma glucose, and triglyceride concentration. However, starvation treatment had a significant effect on glucose tolerance, and the plasma glucose concentration of the S group was significantly lower (<0.05) than that of the other groups during the entire sampling period, whereas liver glycogen content peaked at 6 h. Starvation treatment had a significant effect on activities of carbohydrate metabolic enzymes. Starvation induced the liver PEPCK enzyme activity but depressed PK and PFK enzyme activities. However, PEPCK, PK, and PFK enzyme activities returned to their previous levels after refeeding. After glucose injection, a significant increase (<0.05) in GK and PK activities was observed in the S group, but PK activities of the R group significantly increased (<0.05) and then decreased. Starvation treatment had a significant effect on the expression of in hepatic and muscle tissues. After the glucose load, starvation and refeeding significantly induced the expression of GLUT1 expression in the muscle tissue of the R group decreased, whereas its expression in the muscle tissue of the S group was significantly higher than that of the other groups during the entire sampling period (<0.05). It could be concluded that during the stages of starvation, to deal with the challenges of food deprivation, grass carp depleted glycogen and triglyceride, suppressed hepatic glycolysis enzymes, such as PK and PFK, and activated hepatic glycogenolytic enzymes, such as PEPCK. The results of starvation treatment in grass carp favored the improvement of glucose tolerance through inducing GK and PK enzyme activities, increasing the synthesis of liver glycogen, and activating the expression of in hepatic and muscle tissues.

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李锐鑫,刘泓宇,谭北平,董晓慧,迟淑艳,杨奇慧,章双.饥饿及再投喂处理对草鱼生长、葡萄糖代谢和转运蛋白1表达的影响[J].中国水产科学,2018,25(1):74-85
LI Ruixin, LIU Hongyu, TAN Beiping, DONG Xiaohui, CHI Shuyan, YANG Qihui, ZHANG Shuang. Effects of starvation and refeeding on growth performance, glucose metabolism, and expression of glucose transporter 1 in Ctenopharyngodon idellus[J]. Journal of Fishery Sciences of China,2018,25(1):74-85

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  • 在线发布日期: 2018-01-19
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