[신간의 별자리x] 우리/미술, 그리고 ‘슬픔의 박물관’

Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction

Reactive oxygen species

Unsustainable fishing practices have placed a heavy emphasis on aquaculture to meet the global shortfalls in the supply of fish and seafood, which are commonly accepted as the primary source of health-promoting essential omega-3 (n-3 highly unsaturated fatty acids). However, dietary fish oil is required for the production of omega-3-rich farmed fish and this commodity, in a vicious circle, is at present derived solely from wild fisheries. Decreasing global availability coupled with the highly variable price of this resource has forced the aquaculture industry to investigate the possibilities of alternative dietary lipid sources. This review attempts to compile all principal information available regarding the effects of fish oil replacement for the diets of farmed finfish, analysing the findings using a comparative approach among different cultured fish species. The review initially focuses on the present situation with regard to the production, availability and main nutritional characteristics of fish oil and the principal alternative lipid sources (such as vegetable oils and animal fats). Following this, the effects of fish oil replacement in finfish nutrition on feed quality, fish performance, feed efficiency, fish lipid metabolism, final eating quality and related economic aspects are presented and discussed.

Fish oil replacement in finfish nutrition

Essential fatty acids (EFA) remain one of the least well-understood and enigmatic nutrients in aquaculture nutrition. Of all dietary nutrients none has a greater direct impact on the composition of its consumer. Their importance stems not only to their impact on animal growth, but also to factors such as reproduction, immunity and product quality. Docosahexaenoic acid (DHA; 22:6n-3) has consistently been shown to provide the greatest EFA value to most species. However, the nutritional value of eicosapentaenoic (EPA; 20:5n-3) and arachidonic (ARA; 20:4n-6) acids has also been significantly greater than that exhibited by linolenic (LNA; 18:3n-3) and linoleic (LOA; 18:2n-6) acids. All five fatty acids have been shown to provide EFA value to most aquaculture species, although the optimal dietary inclusion levels and balance among the fatty-acid classes (n-3 and n-6) and fatty-acid chain lengths (18-C, 20-C or 22-C) vary among species. Environmental origin (freshwater, estuarine or marine) appears to be a primary factor influencing the difference in EFA requirements. The role that EFA play in osmoregulation clearly shows how these nutrients affect animals from different aquatic environments. The influence of EFA on growth also appears to be greatest in larval fish and crustaceans, possibly because of their reduced ability to digest and absorb lipids, but also because of a proportionally higher demand for EFA in the development of, in particular, neural tissues. Despite an abundance of research since the 1970s on the EFA requirements of aquaculture species there remains a need to better define the EFA requirements of most aquaculture species. Of all major aquaculture species only the penaeid shrimp has a comprehensively documented assessment of its nutritional requirements for EFA. The nutritional requirements for EFA in most fish species have not been comprehensively studied and those species that were fully examined in the 1970s and 1980s now need to be reassessed in light of recent changes to the use of high-nutrient-density diets that were not routinely used in either practice or research during that earlier period. In addition to changes in dietary specification strategies, declining dependence on marine-origin lipid sources in recent years has placed an increased imperative on understanding the dietary need for long-chain polyunsaturated fatty acids (lcPUFA). As aquaculture continues to grow there will be an increased use of alternative lipid resources, such as grain, algal and rendered oils, to provide dietary lipids. In addition to dietary dilution of natural EFA sources through the use of these raw materials, they will also bring new challenges, such as increased levels of n-6 and 18-C polyunsaturated fatty acids (PUFA). Introduction of these n-6 and PUFA fatty acids to the diet of aquaculture species will not only influence the nutritional demands of these animals, but will also affect their flesh quality characteristics by reducing their level of n-3 lcPUFA. This dilemma will demand an increased prioritisation on the value of lipid sources rich in n-3 lcPUFA, but is also likely to stimulate the development of alternative sources of lcPUFA.

https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1753-5131.2009.01006.x

Exploring the nutritional demand for essential fatty acids by aquaculture species

Effect of dietary lipid level on growth performance, lipid deposition, hepatic lipogenesis in juvenile cobia (Rachycentron canadum)

http://www.hinter.com.cn/Upload/pdf/en/4.pdf

Effects of dietary mannan oligosaccharide on growth performance, gut morphology and stress tolerance of juvenile Pacific white shrimp, Litopenaeus vannamei.

Toxic effects and residue of aflatoxin B1 in tilapia (Oreochromis niloticus × O. aureus) during long-term dietary exposure

High-fat diets may have favourable effects on growth of some carnivorous fish because of the protein-sparing effect of lipids, but high-fat diets also exert some negative impacts on flesh quality. The goal of the study was therefore to determine the effects of fat-enriched diets in juvenile grass carp (Ctenopharyngodon idella) as a typical herbivorous fish on growth and possible lipid metabolism alterations. Three isonitrogenous diets containing 2, 6 or 10 % of a mixture of lard, maize oil and fish oil (1:1:1, by weight) were applied to fish for 8 weeks in a recirculation system. Data show that feeding diets with increasing lipid levels resulted in lowered feed intake, decreased growth and feed efficiency, and increased mesenteric fat tissue weight. Concomitantly, alteration of lipoprotein synthesis and greater level of lipid peroxidation were apparent in blood. In liver, muscle and mesenteric fat tissue, the percentages of alpha-linolenic acid and DHA were significantly increased or tended to increase with higher dietary lipid levels. Biochemical activity measurements performed on liver showed that, with the increase in dietary lipid level, there was a decrease in both mitochondrial and peroxisomal fatty acid oxidation capacities, which might contribute, at least in part, to the specific accumulation of alpha-linolenic acid and DHA into cells more active in membrane building. On the whole, grass carp have difficulty in energetically utilising excess dietary fat, especially when enriched in n-3 PUFA that are susceptible to peroxidation.

/pdf/biochemical-hepatic-alterations-and-body-lipid-composition-ydu24st7yr.pdf

Li-Xia Tian

Papers

Effect of dietary lipid level on growth performance, lipid deposition, hepatic lipogenesis in juvenile cobia (Rachycentron canadum)

Effects of dietary mannan oligosaccharide on growth performance, gut morphology and stress tolerance of juvenile Pacific white shrimp, Litopenaeus vannamei.

Toxic effects and residue of aflatoxin B1 in tilapia (Oreochromis niloticus × O. aureus) during long-term dietary exposure

Biochemical hepatic alterations and body lipid composition in the herbivorous grass carp (Ctenopharyngodon idella) fed high-fat diets.

Dietary l-methionine requirement of juvenile grouper Epinephelus coioides at a constant dietary cystine level