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鸭油甘油二酯与维生素D3协同对肥胖SD大鼠器官指数、血液25羟基维生素D3含量、胫骨发育指标及肝脏维生素D受体和过氧化酶体增殖物激活受体α基因表达量的影响

  • 刘亚楠 ,
  • 王宝维 ,
  • 葛文华 ,
  • 张名爱 ,
  • 孙京新 ,
  • 孔敏
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  • 1. 青岛农业大学食品科学与工程学院, 青岛 266109;
    2. 国家水禽产业技术体系营养与饲料功能研究室, 青岛 266109
刘亚楠(1995-),女,山东荣成人,硕士研究生,研究方向为营养与保健。E-mail:657347874@qq.com

收稿日期: 2019-07-22

  网络出版日期: 2020-01-19

基金资助

国家水禽产业技术体系专项基金(CARS-43-11);山东省2018年度农业重大应用技术创新项目

Effects of Combination of Duck Oil Diglyceride and Vitamin D3 on Organ Indexes, Blood 25 Hydroxyl Vitamin D3 Content, Tibia Development Indexes and Liver Vitamin D Receptor and Peroxisome Proliferators-Activated Receptors α Gene Expressions of Obese SD Rats

  • LIU Yanan ,
  • WANG Baowei ,
  • GE Wenhua ,
  • ZHANG Ming ,
  • SUN Jingxin ,
  • KONG Min
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  • 1. Department of Food Science and Engineering, Qingdao Agricultural University, Qingdao 266109, China;
    2. National Waterfowl Industry Technical System Nutrition and Feed Function Laboratory, Qingdao 266109, China

Received date: 2019-07-22

  Online published: 2020-01-19

Supported by

 

摘要

本试验旨在研究鸭油甘油二酯与维生素D3协同对肥胖SD大鼠器官指数、血液25羟基维生素D3含量、胫骨发育指标及肝脏维生素D受体(VDR)和过氧化酶体增殖物激活受体α(PPARα)基因表达量的影响,以探索鸭油甘油二酯与维生素D3的协同作用。试验选取60只雄性SD大鼠,随机分为4个组(对照组、肥胖模型组、维生素D3组、鸭油甘油二酯+维生素D3组),每组3个重复,每个重复5只。1~3周,对照组饲喂基础饲粮,其他各组饲喂高脂饲粮进行肥胖造模;4~6周,造模成功后,对照组饲喂基础饲粮,肥胖模型组饲喂高脂饲粮,维生素D3组、鸭油甘油二酯﹢维生素D3组在高脂饲粮中添加12.5 μg/kg维生素D3,鸭油甘油二酯+维生素D3组灌胃1 mL/(kg·BW d)鸭油甘油二酯,其他各组灌胃等量的蒸馏水。试验期6周。结果表明,与肥胖模型组相比:1)鸭油甘油二酯与维生素D协同能够显著降低肝脏指数(P<0.05),对心脏、脾脏、肾脏指数无显著影响(P>0.05);2)鸭油甘油二酯与维生素D3协同能够显著升高1、2、3周末的血液25羟基维生素D3含量(P<0.05);3)鸭油甘油二酯与维生素D3协同能够显著提高胫骨的骨密度、骨强度(P<0.05),显著降低血液骨源性碱性磷酸酶活性(P<0.05);4)鸭油甘油二酯与维生素D3协同能够显著上调肝脏VDRPPARα基因表达量(P<0.05)。由此可见,鸭油甘油二酯与维生素D3协同能够降低肥胖大鼠肝脏指数,提高血液25羟基维生素D3含量,上调肝脏VDRPPARα基因表达量,促进胫骨发育。

本文引用格式

刘亚楠 , 王宝维 , 葛文华 , 张名爱 , 孙京新 , 孔敏 . 鸭油甘油二酯与维生素D3协同对肥胖SD大鼠器官指数、血液25羟基维生素D3含量、胫骨发育指标及肝脏维生素D受体和过氧化酶体增殖物激活受体α基因表达量的影响[J]. 动物营养学报, 2020 , 32(1) : 472 -480 . DOI: 10.3969/j.issn.1006-267x.2020.01.055

Abstract

This experiment was conducted to study the effects of duck oil diglyceride and vitamin D3 coordination on organ indexes, blood 25 hydroxyl vitamin D3 content, tibia development indexes and liver vitamin D receptor (VDR) and peroxisome proliferators-activated receptors α (PPARα) gene expressions of obese SD rats, to explore the synergistic relationship between duck oil diglyceride and vitamin D3. Sixty male SD rats were randomly assigned into 4 groups (control group, obese model group, vitamin D3 group and duck oil diglyceride+vitamin D3 group) with 3 replicates per group and 5 rats per replicate. During 1 to 3 weeks, rats in the control group were fed a basal diet, and the others in other groups were fed high-fat diets for obesity modeling. During 4 to 6 weeks, after successful modeling, rats in the control group were fed a basal diet, rats in the obese model group were fed a high-fat diet, rats in vitamin D3 group and duck oil diglyceride+vitamin D3 group were fed high-fat diet supplemented 12.5 μg/kg vitamin D3, rats in duck oil diglyceride+vitamin D3 group were given 1 mL/(kg·BW d) duck oil diglyceride by gavage, and rats in other groups were given the same amount of distilled water by gavage. The experiment lasted for 6 weeks. The results showed that compared with the obese model group:1) the combination of duck oil diacylglycerol and vitamin D3 could significantly reduce the liver index (P<0.05), but had no significant effect on the indexes of heart, spleen and kidney (P>0.05); 2) the combination of duck oil diglyceride and vitamin D3 could significantly increase the blood 25 hydroxy vitamin D3 content (P<0.05); 3) the combination of duck oil diglyceride and vitamin D could significantly increase the bone density and bone strength in tibia (P<0.05), and significantly decreased the blood bone derived alkaline phosphatase activity (P<0.05); 4) the combination of duck oil diglyceride and vitamin D3 could significantly increase the liver VDR and PPARα gene expressions (P<0.05). In conclusion, the combination of duck oil diglyceride and vitamin D3 can decrease the liver index of obese rats, increase the blood 25 hydroxy vitamin D3 content, increase the liver VDR and PPARα gene expressions, and promote the development of tibia.

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