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生态学杂志 ›› 2023, Vol. 42 ›› Issue (1): 146-151.doi: 10.13292/j.1000-4890.202301.007

• 研究报告 • 上一篇    下一篇

长期饥饿下熊本牡蛎生理代谢和酶活性变化

王杰1,2,李雪英2,陈启沂1,2,张扬1,2,唐保军2*


  

  1. 1上海海洋大学水产与生命学院, 上海 201306; 2中国水产科学研究院东海水产研究所, 上海 200090)

  • 出版日期:2023-01-10 发布日期:2023-02-01

Changes of physiological metabolism and enzyme activities of Crassostrea sikamea under long-term starvation.

WANG Jie1,2, LI Xue-ying2, CHEN Qi-yi1,2, ZHANG Yang1,2, TANG Bao-jun2*   

  1. (1College of Fisheries and Life Science, Shanghai Ocean University, Shanghai 201306, China; 2East China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Shanghai 200090, China).

  • Online:2023-01-10 Published:2023-02-01

摘要: 为了探讨熊本牡蛎(Crassostrea sikamea)在长期饥饿胁迫下的生理代谢响应,测定了长期饥饿(0~80 d)以及再投喂(90~118 d)状态下熊本牡蛎的耗氧率、排氨率以及肝胰腺组织乳酸脱氢酶、琥珀酸脱氢酶、丙酮酸激酶、超氧化物歧化酶、碱性磷酸酶和溶菌酶的活性。结果表明:长期饥饿下,熊本牡蛎的耗氧率和排氨率极显著降低(P<0.01);随着饥饿时间的延长,熊本牡蛎乳酸脱氢酶、琥珀酸脱氢酶、丙酮酸激酶、超氧化物歧化酶和碱性磷酸酶活性均呈现波动下降的趋势,溶菌酶活性呈现波动上升的趋势;再投喂后熊本牡蛎的耗氧率、排氨率均极显著升高(P<0.01);长期饥饿对熊本牡蛎代谢和免疫功能造成损伤,熊本牡蛎通过降低代谢率和代谢酶的活性应对长期饥饿胁迫。本研究可为海水贝类饥饿胁迫下代谢调节机制的研究提供参考。


关键词: 熊本牡蛎, 饥饿胁迫, 耗氧率, 排氨率, 酶活性

Abstract: To clarify the physiological and metabolic responses of Crassostrea sikamea under long-term starvation stress, we measured oxygen consumption rate, ammonia excretion rate and activities of lactate dehydrogenase, succinate dehydrogenase, pyruvate kinase, superoxide dismutase, alkaline phosphatase and lysozyme in hepatopancreas after long-term starvation (0-80 d) and refeeding (90-118 d). The results showed that oxygen consumption and ammonia excretion rate of C. sikamea decreased significantly under long-term starvation (P<0.01). With the prolongation of starvation, the activities of lactate dehydrogenase, succinate dehydrogenase, pyruvate kinase, superoxide dismutase, and alkaline phosphatase in C. sikamea showed a trend of fluctuating decline, while lysozyme activity showed a trend of fluctuating rise. After refeeding, oxygen consumption and ammonia excretion rate of C. sikamea significantly increased (P<0.01). Long-term starvation may damage the metabolism and immune functions of C. sikamea, and C. sikamea, and they respond to long-term starvation stress by reducing metabolic rate and metabolic enzyme activities. Our results provide a reference for the study of metabolic regulation mechanism of marine shellfish under starvation stress.


Key words: Crassostrea sikamea, starvation stress, oxygen consumption rate, ammonia excretion rate, enzymatic activity.