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A Simple Approach to Manipulate Dissolved Oxygen for Animal Behavior Observations
Published on: June 28, 2016
Dissolved oxygen regulates density-driven accumulation of waterborne L-DOPA and physiological homeostasis in turbot
Xi Wang1, Shiqi Li2, Zhiyi Wang2
1Marine Organism Water Environment Engineering Laboratory, College of Fisheries, Ocean University of China, PR China; Key Laboratory of Mariculture (Ministry of Education), College of Fisheries, Ocean University of China, Qingdao, 266001, PR China; Shandong Key Laboratory of Green Mariculture and Smart Fisheries, PR China.
Abstract:
High stocking density in recirculating aquaculture systems (RAS) can promote the accumulation of endogenous bioactive metabolites, yet the environmental factors controlling their formation remain unclear. L-3,4-dihydroxyphenylalanine (L-DOPA) has recently linked to growth inhabitation in crowded turbot (Scophthalmus maximus) culture. Here, we used a 2 × 2 factorial design with two dissolved oxygen (DO) levels (HDO, 10 mg/L; NDO, 7 mg/L) and two stocking densities (HD, 9.39 kg/m2; LD, 4.70 kg/m2) to examine whether oxygen availability regulates waterborne L-DOPA accumulation and associated biological effects in turbot RAS. After 60 days, fish under normoxic conditions and high density (NDO-HD) showed marked growth inhibition, whereas HDO restored growth to levels comparable with low-density treatments. Waterborne L-DOPA in the NDO-HD group increased to approximately twice that in the other groups, while HDO prevented this density-associated accumulation. Elevated L-DOPA coincided with increased blood methemoglobin, lactate and cortisol, suggesting impaired oxygen transport, enhanced anaerobic metabolism and systemic stress. It was also associated with sustained activation of HIF-1 signaling pathway, including upregulating of hypoxia-inducible factor-1α (hif-1α), erythropoietin (epoa) and EGL nine homolog 1(egln1a), and with disrupted L-DOPA metabolism, characterized by increased tyrosine hydroxylase (th) and reduced phenylalanine hydroxylase (pah) and dopa decarboxylase (ddc) expression. Transcriptomic analysis further indicated that oxygen supplementation reduced stress-related transcriptional responses and supported pathways related to energy metabolism and anabolic growth. These findings identify DO as a key environmental regulator of endogenous L-DOPA accumulation and suggest that oxygen management can reduce endogenous bioactive metabolite buildup in intensive RAS.
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