中国农业科学 ›› 2009, Vol. 42 ›› Issue (11): 4042-4050 .doi: 10.3864/j.issn.0578-1752.2009.11.035

• 畜牧·资源昆虫 • 上一篇    下一篇

日粮添加DHA对肉仔鸡生长及脂肪代谢基因转录的后效作用

李岩,孙超

  

  1. (西北农林科技大学动物科技学院)
  • 收稿日期:2009-05-18 修回日期:2009-06-15 出版日期:2009-11-10 发布日期:2009-11-10
  • 通讯作者: 孙超

The Later Effects of DHA in Diet on Regulating Transcription of Lipid Genes of Broiler

LI Yan, SUN Chao   

  1. (西北农林科技大学动物科技学院)
  • Received:2009-05-18 Revised:2009-06-15 Online:2009-11-10 Published:2009-11-10
  • Contact: SUN Chao

摘要:

【目的】探讨二十二碳六烯酸(DHA)微藻粉对肉仔鸡生长和脂肪代谢的影响及其持续效果,为揭示DHA调节动物脂肪沉积的机理提供依据。【方法】1周龄AA肉仔鸡日粮中添加DHA微藻粉,添加2周,分别在3、4、5周时屠宰,取组织样提总RNA,采用RT-PCR技术检测各组织中基因转录表达。【结果】DHA微藻粉显著增加肉仔鸡日增重和饲料转化率,降低腹脂率,降低血清中总胆固醇TC、甘油三酯TG和低密度脂蛋白胆固醇LDL-C含量,增加高密度脂蛋白胆固醇HDL-C含量(P<0.05),停止添加1周后仍有显著作用(P<0.05)。DHA微藻粉可提高肝脏过氧化物酶增生物激活受体(PPARα)和肉碱酰基转移酶(CPT-1)mRNA表达,抑制脂肪酸合成酶(FAS) mRNA表达,停止添加后,可促进上述基因的表达(P<0.01)。DHA微藻粉能促进乙酰辅酶A羧化酶(ACC)、FAS和 CPT-1 mRNA表达,抑制腹脂中脂蛋白脂酶(LPL)mRMA表达,停止添加后,试验组中各基因表达低于对照组(P<0.01)。DHA微藻粉显著抑制胸肌中脂肪合成和脂肪酸氧化的基因表达(P<0.01),停止添加1周后,试验组中FAS、LPL、CPT-1 mRNA表达高于对照组(P<0.05);停止添加2周后,可抑制脂肪合成与分解基因的表达(P<0.01)。DHA微藻粉显著抑制腿肌中FAS mRNA表达,促进ACC、LPL、CPT-1 mRNA表达;停止添加1周后,显著地抑制合成与分解基因表达(P<0.01);但停止添加2周后,观测到相反现象。【结论】DHA微藻粉对肉仔鸡各组织中脂肪代谢影响不同,在肝脏和腿肌中抑制脂肪合成,促进氧化,停止添加2周后,促进脂肪合成与分解;在脂肪组织中可促进脂肪合成与分解,停止添加后,呈相反作用;在胸肌中抑制脂肪合成与氧化,停止添加后出现相反作用。

关键词: DHA微藻粉, 肉仔鸡, 脂肪组织, 肝脏, 脂类代谢相关基因

Abstract:

【Objective】 The effect of docosahexaenoic acid (DHA) on lipid metabolism in broiler were studied in order to provide test results for PUFA regulating fatty deposition. 【Method】 One-week-old AA Broiler were fed DHA microalgae, and slaughtered after two weeks. The tissues were reserved for isolating total RNA. RT-PCR was used to analyze the expression changes of genes. 【Result】 DHA microalgae significantly increased average body gain and feed conversion rates, reduced the levels of total cholesterol TC, TG and low-density lipoprotein cholesterol in serum, and increased the content of high-density lipoprotein cholesterol. One week later, the effects were still remained. In liver tissue, DHA microalgae increased the expression of PPARα and CPT-1. One week later, it was observed that DHA up-regulated the expression of FAS, ACC, LPL and CPT-1. Two weeks later, it still increased the expression of FAS and CPT-1, but a converse result was observed for ACC and LPL. In adipose tissue, DHA microalgae suppressed the expression of PPARα and LPL, up-regulated the expression of ACC, FAS and CPT-1. After stop adding, the expression of genes in test group were significantly lower than the control group (P<0.01). In the muscle of chest, DHA microalgae significantly inhibited the gene expressions (P<0.01). One week later, the expression of FAS, LPL, CPT-1 in test group were significantly higher than the control group (P<0.05). Two weeks later, it was shown that DHA significantly inhibited fat synthesis and decomposition. In the leg, DHA microalgae significantly declined the expression of FAS, and increased the expression of ACC, LPL, and CPT-1. After one week, the inhibition was still significant. But two weeks later, the contrary result was observed. Chest and leg were not detected a large number of expression of PPARα, probably because of the less expression in muscle tissues or the regulation of PPARα had no relation to the case. 【Conclusion】 DHA microalgae can promote fat synthesis in the liver and inhibit in adipose and muscle tissues. It still has effects after one week of ceasing.

Key words: DHA, broiler, adipose tissue, liver, lipid metabolic genes