饥饿和再投喂期间尼罗罗非鱼生长、血清生化指标和肝胰脏生长激素、类胰岛素生长因子-Ⅰ和胰岛素mRNA表达丰度的变化

The changes in growth, serum biochemical indices and GH/IGF-Ⅰ/IN mRNA expression abundance of Oreochromis niloticus during fasting and re-feeding

  • 摘要: 在室内可控条件下, 对尼罗罗非鱼初始体质量(62.50±3.44) g进行饥饿28 d和随后再投喂21 d的处理, 于饥饿第0、7、14、21、28天和再投喂第14、21天进行采样分析, 研究饥饿和再投喂期间尼罗罗非鱼生长、血清生化指标和肝胰脏生长激素(GH)、类胰岛素生长因子-Ⅰ(IGF-Ⅰ)和胰岛素(IN) mRNA表达丰度的变化。结果显示, 与饥饿第0天相比, 饥饿超过7 d鱼体体质量显著降低(P <0.05), 再投喂21 d显著增加(P <0.05); 肝体比随饥饿时间延长显著降低(P < 0.05), 恢复投喂后较饥饿时升高, 但显著低于饥饿前水平(P<0.05)。在血清指标上, 甘油三酯、血糖、碱性磷酸酶、谷草转氨酶和谷丙转氨酶均随饥饿时间延长而逐渐降低, 恢复投喂后均有不同程度提高, 但转氨酶活性显著低于饥饿前水平(P<0.05); 饥饿和再投喂对血清总胆固醇、高密度脂蛋白胆固醇和低密度脂蛋白胆固醇无显著影响(P>0.05)。在激素方面, 与饥饿第0天相比, 饥饿使血清GH含量及其肝胰脏mRNA表达丰度显著升高, 血清IGF-Ⅰ及其肝胰脏mRNA表达丰度降低, 恢复投喂后两者均显著升高(P<0.05); IN mRNA表达丰度在饥饿7~21 d显著升高(P<0.05), 饥饿第28天时无显著差异(P>0.05), 再投喂后显著降低(P<0.05)。

     

    Abstract: Studies were conducted to reveal the changes in growth, serum biochemical indices and growth hormone (GH), insulin-like growth factor Ⅰ(IGF-Ⅰ) and insulin (IN) mRNA expression abundance of Nile tilapia (Oreochromis niloticus) during fasting and re-feeding. Nile tilapia with initial body weight (62.50 ± 3.44) g were starved for 28 d and then fed for 21 d under controllable indoor environment. Fish were sampled at 0, 7, 14, 21 and 28 d during fasting and at 14 and 21 d during re-feeding, respectively. The results indicated that the body weight was significantly decreased when fasting over 7 d (P<0.05), and significantly increased when re-feeding for 21 d (P<0.05). The hepatosomatic index was significantly decreased throughout the experiment (P<0.05). Significant reduction was observed in the content of triglyceride and glucose, and in the activities of alkaline phosphatase, glutamic oxaloacetic transaminase and glutamic pyruvic transaminase after fasting (P<0.05); After re-feeding, the value of these indices increased in varying degrees, but the activity of transaminase was significantly lower than initial value(P<0.05). There was no change in total cholesterol, high density lipoprotein cholesterol or low density lipoprotein cholesterol during the experiment (P>0.05). Serum GH and liver GH mRNA levels showed significantly up-regulation, whereas significant down-regulation was observed in serum IGF-Ⅰ and liver IGF-Ⅰ mRNA levels after fasting, and after re-feeding both of them increased (P<0.05). IN mRNA level was significantly increased during fasting for 7-21 d (P<0.05), but its level was not obviously changed when fasting for 28 d (P>0.05), then was significantly decreased after re-feeding (P<0.05). The present study revealed that fasting could restrain the growth of O. niloticus, promote serum triglyceride and glucose breakdown, and decrease the activity of transaminase. Serum GH/ IGF-Ⅰ and liver GH/ IGF-Ⅰ mRNA expression abundance displayed synchronous changes and the liver IN mRNA expression abundance was significantly increased when fasting for 7-21 d and then decreased to normal level when fasting for 28 d. It suggests that the level of GH / IGF-Ⅰ gene transcription of O. niloticus may be the most important factor in determining the levels of hormone in serum, while down-regulation of serum insulin may be due to its release reduction in islet when fasting.

     

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