Food-grade fish oil supplementation promotes membrane and redox stability during cryopreservation of aquatic biomaterials
- Food Chem. 2026 May 1:510:148652. doi: 10.1016/j.foodchem.2026.148652.
- 1. Integrative Science Center of Germplasm Creation in Western China Integrative Science Center of Germplasm Creation in Western China (CHONGQING) Science City & College of Fisheries, Southwest University, Key Laboratory of Freshwater Fish Reproduction and Development; Ministry of Education, Key Laboratory of Aquatic Sciences of Chongqing, 402460, Chongqing.
- 2. Integrative Science Center of Germplasm Creation in Western China Integrative Science Center of Germplasm Creation in Western China (CHONGQING) Science City & College of Fisheries, Southwest University, Key Laboratory of Freshwater Fish Reproduction and Development; Ministry of Education, Key Laboratory of Aquatic Sciences of Chongqing, 402460, Chongqing. Electronic address: [email protected].
- 3. Integrative Science Center of Germplasm Creation in Western China Integrative Science Center of Germplasm Creation in Western China (CHONGQING) Science City & College of Fisheries, Southwest University, Key Laboratory of Freshwater Fish Reproduction and Development; Ministry of Education, Key Laboratory of Aquatic Sciences of Chongqing, 402460, Chongqing. Electronic address: [email protected].
The development of food-compatible strategies represents a critical advancement for the cryopreservation of aquatic biomaterials. This study evaluated the efficacy of food-grade fish oil (FO) as a synergistic adjunct within a standard DMSO-based cryomedium. Supplementation with 0.1% FO significantly increased the post-thaw viability of fish ovarian cells from 63.52% to 78.25% compared to the control (n = 6 biological replicates). Ultrastructural and functional analyses confirmed that FO treatment effectively maintained mitochondrial integrity (n = 3) and membrane potential (n = 6). Furthermore, FO supplementation mitigated oxidative stress by lowering MDA levels and modulating the expression of stress-response genes, specifically downregulating HSP70 and lamp3 (n = 6). Crucially, functional recovery was demonstrated by a shortened population doubling time (206.71 h, n = 6) and a 36.67% engraftment efficiency in a xenotransplantation model (n = 3). These findings establish FO as a potent, food-compatible supplement for optimizing conventional cryopreservation protocols in biotechnology.
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Cat. No.Product NameDescriptionTargetResearch Area
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target: Biochemical Assay ReagentsResearch Areas: Neurological Disease