scholarly journals Based on the Metabolomic Approach the Energy Metabolism Responses of Oriental River Prawn Macrobrachium nipponense Hepatopancreas to Acute Hypoxia and Reoxygenation

2018 ◽  
Vol 9 ◽  
Author(s):  
Shengming Sun ◽  
Zhongbao Guo ◽  
Hongtuo Fu ◽  
Xianping Ge ◽  
Jian Zhu ◽  
...  
Keyword(s):  
Energy Metabolism ◽  
Acute Hypoxia ◽  
Macrobrachium Nipponense ◽  
Oriental River Prawn ◽  
Metabolomic Approach

Effects of nanoplastics on energy metabolism in the oriental river prawn (Macrobrachium nipponense)

2021 ◽  
Vol 268 ◽  
pp. 115890
Author(s):  
Yiming Li ◽  
Zhiquan Liu ◽  
Yuan Yang ◽  
Qichen Jiang ◽  
Donglei Wu ◽  
...  
Keyword(s):  
Energy Metabolism ◽  
Macrobrachium Nipponense ◽  
Oriental River Prawn

scholarly journals Molecular Cloning and Expression of MnGST-1 and MnGST-2 from Oriental River Prawn, Macrobrachium nipponense, in Response to Hypoxia and Reoxygenation

2018 ◽  
Vol 19 (10) ◽  
pp. 3102 ◽  
Author(s):  
Lei Xu ◽  
Ming Yang ◽  
Hongtuo Fu ◽  
Shengming Sun ◽  
Hui Qiao ◽  
...  
Keyword(s):  
Intracellular Transport ◽  
Expression Profiles ◽  
Acute Hypoxia ◽  
Cloning And Expression ◽  
Glutathione S Transferase ◽  
Specific Expression ◽  
Macrobrachium Nipponense ◽  
Hypoxia Stress ◽  
Oriental River Prawn ◽  
Specific Expression Pattern

The glutathione-S-transferase (GST) superfamily includes seven classes, and different classes have different functions. GST superfamily members function in various processes including detoxification of xenobiotics, protection against oxidative damage, and intracellular transport of hormones, endogenous metabolites, and exogenous chemicals. Herein, to elucidate the tissue-specific expression pattern of GSTs in response to hypoxia stress, which induces cell death, we investigated the expression of GSTs in response to hypoxia and reoxygenation in oriental river prawn, Macrobrachium nipponense. Full-length cDNAs of two δ class GSTs were cloned from the hepatopancreas, and named MnGST-1 and MnGST-2 based on the established GST nomenclature system. Expression profiles of both GSTs in various tissues were different under acute and chronic experimental hypoxia stress conditions, suggesting that both respond strongly to hypoxia-induced oxidative stress. However, the intensity of responses to hypoxia and reoxygenation were different in different tissues. During acute hypoxia stress, MnGST-1 responds earlier than MnGST-2 in the hepatopancreas and gill, but more slowly in muscle. By contrast, during chronic hypoxia stress, MnGST-2 plays a more important role in the hepatopancreas and gill than MnGST-1.

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