اثر افزودن تورین و پودر چربی به جیره غذایی بر شاخص‌های رشد، ترکیب بیوشیمیایی بدن و هضم‌پذیری چربی قزل‌آلای رنگین کمان انگشت قد (Oncorhynchus mykiss)

نوع مقاله : مقاله پژوهشی

نویسندگان

گروه شیلات، دانشکده علوم دامی و شیلات، دانشگاه علوم کشاورزی و منابع طبیعی ساری، ساری، مازندران

چکیده

پودر چربی به عنوان یک چربی با اسیدهای چرب اشباع و هضم‌پذیری کم است. لذا استفاده از مکمل‌های مناسب شاید بتواند امکان جایگزینی این منبع چربی را در جیره افزایش دهد. هدف از تحقیق حاضر بررسی تأثیر تورین بر رشد، ترکیب بدن و هضم­پذیری چربی ماهی قزل­آلای رنگین­کمان (Oncorhynchus mykiss) تغذیه شده با پودر چربی بود. جیره‌های آزمایشی (40% پروتئین و 23% چربی) شامل کنترل مثبت حاوی روغن ماهی و روغن کانولا و دیگر جیره‌ها شامل پودر چربی g/kg 76 و تورین در سطوح صفر (کنترل منفی)، 5، 10 و g/kg  20 بود. 225 قطعه قزل‌آلای رنگین‌کمان با میانگین وزنی 03/0 ± 12 گرم به مدت 58 روز با جیره­های آزمایشی تغذیه شدند. نتایج حاصله نشان داد افزودنg/kg  20 تورین به جیره حاوی پودر چربی منجر به افزایش معنی­دار درصد افزایش وزن بدن و نرخ رشد ویژه در مقایسه با جیره کنترل منفی فاقد تورین شد (05/0>P)؛ در حالی که ضریب تبدیل غذایی، غذای مصرف شده، کارایی پروتئین، فاکتور وضعیت و بازماندگی ماهیان تحت تأثیر جیره‌های آزمایشی قرار نگرفت (05/0<P). همچنین، پروتئین و چربی بدن ماهیان تغذیه ‌شده با g/kg 20 تورین در مقایسه با کنترل منفی افزایش یافت (05/0>P). خاکستر بدن در جیره کنترل مثبت به طور معنی‌‌داری بالاتر از جیره کنترل منفی بود (05/0>P). علاوه بر این، هضم‌پذیری پروتئین و خاکستر در تیمارهای دارای تورین g/kg 20 بیشترین مقدار و در تیمار کنترل منفی کمترین مقدار بود. با توجه به نتایج این تحقیق، افزودنg/kg  20 تورین به عنوان مناسب‌ترین سطح مکمل به جیره حاوی 70% پودر چربی در قزل­آلا اثرات مثبت معنی‌داری بر رشد، ترکیب بدن و هضم­پذیری چربی دارد.

کلیدواژه‌ها

موضوعات


عنوان مقاله [English]

Effects of adding taurine and fat powder to the diet on growth indices, body biochemical composition and fat digestibility of rainbow trout Oncorhynchus mykiss fingerlings

نویسندگان [English]

  • Fatemeh Norouzi
  • Sakineh Yeganeh
  • Farid Firouzbakhsh
  • Batoul Adhami
Department of Fisheries, Faculty of Animal Science and Fisheries, Sari Agricultural Sciences and Natural Resources University, Sari, Mazandaran, Iran
چکیده [English]

Introduction: Rainbow trout, Oncorhynchus mykiss belongs to the Salmonid family, one of the important domestic species in freshwater. High-energy diets with approximate levels of 45-50% protein and 18-24% fat are considered to meet their demands. However, due to the limited availability of fish oil, it cannot be considered a sustainable fat source in aquaculture. Meanwhile, fat powder can be used as an available and sustainable alternative in the diet, but due to the presence of saturated fatty acids, it has low digestibility, which may adversely affect fish health and growth. Thus, suitable additives might increase the possibility of replacing fat powder in the diet. Additionally, the amino acid taurine plays a crucial role in the formation of bile salts, which are essential for the digestion and absorption of intestinal fats. This study aims to investigate the effect of supplementary taurine on the growth, body composition, and fat digestibility of rainbow trout fed fat powder, with a focus on optimizing aquaculture productivity and sustainability.
Materials and Methods: Experimental diets included a positive control containing fish oil, canola oil and other diets containing fat powder (about 70% of the fat source was provided) supplemented with taurine at doses of 0 (negative control), 5, 10, and 20 g/kg (T0, T5, T10 and T20, respectively). A total of 225 rainbow trout with an average initial weight of 12 ± 0.03 g were distributed in 15 rearing tanks based on a completely randomized design for 58 days. Fish were fed three times a day at 8:00, 12:00 and 18:00 until apparent satiation. After 24 hours of stop feeding, the approximate amount of body composition (sampling of three fish from each tank at the end of the experiment) and items including protein, moisture, total fat and ash were measured followed by the procedure of AOAC (2005). At the end of the experiment, in order to evaluate the apparent digestibility of nutrients, fish were fed with diets containing chromic oxide. Then, feed and feces were collected and analyzed according to the method described by Austreng (1978). SPSS software (version 19.0) was used for statistical analysis. Data were presented as the mean of 3 replicates ± standard deviation using the Duncan post-hoc test to compare means of each treatment.
Results: The results of growth parameters showed that T20 exhibited in a significant increase in final weight, percentage of weight gain and specific growth rate compared to the negative control (T0; P<0.05) Feed conversion ratio, feed intake, protein efficiency, condition factor and survival rate were not affected by the experimental diets (P<0.05). According to the result of body composition, fat, protein and ash contents were affected by the different levels of taurine (P<0.05), but moisture did not show a significant difference between the experimental treatments (P<0.05). T20 resulted in an increase in protein and fat compared to the negative control (P<0.05). Body fat content was higher in the positive control than in the other groups (P<0.05). The lowest body fat content was related to T20. (P<0.05). Body protein was improved in T20 similar to the positive control (P<0.05), and the lowest amount of protein was found in the negative control (P<0.05). The ash content in the positive control was significantly higher than in the negative control (P<0.05). Furthermore, T20 led to an increase in protein digestion, while the lowest value was observed in the negative control (P<0.05). The fat digestibility was negatively affected by fat powder inclusion. However, it could be improved to some extent when taurine was supplemented. The highest ash content was found in T20 whereas the lowest in the negative control (P<0.05).
Discussion: The results of the present study indicate that the addition of 20 g/kg taurine to a diet containing fat powder (T20) improves the growth performance of fish. This improvement is likely due to the enhanced fat digestion and better fat utilization as an energy source. Furthermore, T20 resulted in elevated body protein and fat content. Although the body fat in fish treated with the positive control was higher than in the other treatments, T20 seems to fully compensate the body protein levels. The increased body fat suggests improved digestibility of fat powder under the influence of taurine. Taurine has a significant role in enhancing fat digestion by binding to bile acids, leading to the formation of bile salts. These bile salts are stored in the gallbladder and released into the intestine as required, facilitating the digestion and absorption of fats. Taurine increases protein synthesis by accelerating glycolysis and fulfills the growth requirements of the fish body through intense oxidative glucose breakdown or its conversion into amino acids. The current findings showed that protein digestibility improved by diets containing 10 and 20 g/kg taurine (T10 and T20). On the other hand, the inclusion of fish oil in the diet, due to its polyunsaturated fatty acids with multiple double bonds, demonstrates greater digestibility compared to fat powders. The observed reduction in digestibility in the negative control group can be attributed to the insufficiency of bile salts, but this could be compensated by the addition of taurine.
Conclusion: Given the results, it can be concluded that the addition of taurine successfully improved the digestibility of fat powder in the diet of rainbow trout. As a result, taurine enhanced fat absorption, and at the level of 20 g/kg taurine, it also improved protein digestibility. These improvements led to enhanced growth performance and increased body protein in rainbow trout.

کلیدواژه‌ها [English]

  • Amino acid
  • Supplement
  • Fat substitution
  • Saturated fatty acids
  • Development of aquaculture
Adhami, B., Karamat, A., Orji, H., Kazemifard, M., Mahjoob, S. 2021. Effect of lysophospholipid on growth performance, blood parameters, liver enzymes, and lysozyme activity of rainbow trout Oncorhynchus mykiss fed a diet containing fat powder. Fisheries Science and Technology 10: 272-285. DOI: 20.1001.1.23225513.1400.10.3.4.8.
Amirkolaie, A.K., Shahkolaie, M.D., Karimzadeh, S., Khalesi, M. 2014. The potential of soya oil industry products as oil alternatives in rainbow trout Onchorhyncus mykiss diet. Aquaculture International 22: 1093-1103. DOI: 10.1007/s10499-013-9730-x.
AOAC. 2005. Official Methods of Analysis of the Association of Official Analytical Chemists, 16th ed. Association of Official Analytical Chemists, Washington DC, USA.
Austreng, E. 1978. Digestibility determination in fish using chromic oxide marking and analysis of contents from different segments of the gastrointestinal tract. Aquaculture 13: 265-272. DOI: 10.1016/0044-8486(78)90008-X.
Carr, I., Glencross, B., Santigosa, E., 2023. The importance of essential fatty acids and their ratios in aquafeeds to enhance salmonid production, welfare, and human health. Frontiers in Animal Science 4: 1147081. DOI: 10.3389/fanim.2023.1147081.
Chatzifotis, S., Polemitou, I., Divanach, P., Antonopoulou, E. 2008. Effect of dietary taurine supplementation on growth performance and bile salt activated lipase activity of common dentex, Dentex dentex, fed a fish meal/soy protein concentrate-based diet. Aquaculture 275: 201-208. DOI: 10.1016/j.aquaculture.2007.12.013.
Chen, Y., Sun, Z., Liang, Z., Xie, Y., Su, J., Luo, Q., Zhu, J., Liu, Q., Han, T., Wang, A. 2020. Effects of dietary fish oil replacement by soybean oil and L-carnitine supplementation on growth performance, fatty acid composition, lipid metabolism and liver health of juvenile largemouth bass, Micropterus salmoides. Aquaculture 516: 734596. DOI: 10.1016/j.aquaculture.2019.734596.
Cotou, E., Miliou, H., Chatzoglou, E., Schoina, E., Politakis, N., Kogiannou, D., Fountoulaki, E., Androni, A., Konstantinopoulou, A., Assimakopoulou, G., Nathanailides, C. 2024. Growth performance and environmental quality indices and biomarkers in a co-culture of the European sea bass with filter and deposit feeders: a case study of an IMTA system. Fishes 9: 69. DOI: 10.3390/fishes9020069.
De Moura, L.B., Diógenes, A.F., Campelo, D.A., de Almeida, F.L., Pousão-Ferreira, P.M., Furuya, W.M., Oliva-Teles, A., Peres, H. 2018. Taurine and methionine supplementation as a nutritional strategy for growth promotion of meagre Argyrosomus regius fed high plant protein diets. Aquaculture 497: 389-395. DOI: 10.1016/j.aquaculture.2018.07.038.
Ebrahimi Dorcheh, E., Zare, P. 2011. Effects of dietary lipid level on growth, feed utilization and survival of juvenile of Beluga Huso huso. Journal of Natural Environmental. Iranian Journal of Natural Resources 64: 93-106.
El-Sayed, A.F.M. 2013. Is dietary taurine supplementation beneficial for farmed fish and shrimp? A comprehensive review. Reviews in Aquaculture 6: 241-255. DOI: 10.1111/raq.12042.
Espe, M., Ruohonen, K., El‐Mowafi, A. 2012. Effect of taurine supplementation on the metabolism and body lipid‐to‐protein ratio in juvenile Atlantic salmon Salmo salar. Aquaculture Research 43: 349-360. DOI: 10.1111/j.1365-2109.2011.02837.x.
Eslami, M., Bahrekazemi, M. 2022. Effect of different dietary-taurine on growth, feeding performance, digestive enzymes and immunity of beluga, Huso huso, under the low water temperature. Journal of Fisheries 75: 49-62. DOI: 10.22059/jfisheries.2021.329862.1279.
FAO. 2024. The State of World Fisheries and Aquaculture 2024: Blue Transformation in Action. 1st ed. FAO. Rome, Italy.
Ferreira, F.M., Yun, H., Park, Y., Park, G., Choi, S., Bai, S.C. 2014. Effects of taurine supplementation on the growth performance of juvenile rock bream Oplegnathus fasciatus. Fisheries and Aquatic Science 17: 255-261. DOI: 10.5657/FAS.2014.0255.
Garcia-Organista, A.A., Mata-Sotres, J.A., Viana, M.T., Rombenso, A.N. 2019. The effects of high dietary methionine and taurine are not equal in terms of growth and lipid metabolism of juvenile California yellowtail Seriola dorsalis. Aquaculture 512: 734304. DOI: 10.1016/j.aquaculture.2019. 734304.
Ghorbani, R., Yousefi Jourdehi, A. 2020. Comparison of nutritional requirements (crude protein, crude fat and carbohydrates) of sturgeon and rainbow trout Oncorhynchus mykiss in rearing conditions. Sturgeon 2: 1-7.
Goto, T., Takagi, S., Ichiki, T., Sakai, T., Endo, M., Yoshida, T., Ukawa, M., Murata, H. 2001. Studies on the green liver in cultured red sea bream fed low level and non-fish meal diets: Relationship between hepatic taurine and biliverdin levels. Fisheries Sciences 67: 58-63. DOI: 10.1046/j.1444-2906.2001.00199.x.
Hardy, R.W. 2010. Utilization of plant proteins in fish diets: effects of global demand and supplies of fishmeal. Aquaculture Research 41: 770-776. DOI: 10.1111/j.1365-2109.2009.02349.x.
Huang, M., Yang, X., Zhou, Y., Ge, J., Davis, D.A., Dong, Y., Gao, Q., Dong, S. 2021. Growth, serum biochemical parameters, salinity tolerance and antioxidant enzyme activity of rainbow trout Oncorhynchus mykiss in response to dietary taurine levels. Marine Life Science and Technology 1-14. DOI: 10.1007/s42995-020-00088-2
Ketels, E. 1994. The metabolizable energy values of fats in poultry diets. Master of Science, Faculty of Agricultural and Applied Biological Sciences, University of Gent, Belgium.
Kim, S.K., Matsunari, H., Takeuchi, T., Yokoyama, M., Murata, Y., Ishihara, K. 2007. Effect of different dietary taurine levels on the conjugated bile acid composition and growth performance of juvenile and fingerling Japanese flounder Paralichthys olivaceus. Aquaculture 273: 595-601. DOI: 10.1016/j.aquaculture.2007.10.031.
Kim, S.K., Matsunari, H., Takeuchi, T., Yokoyama, M., Furuita, H., Murata, Y., Goto, T. 2008. Comparison of taurine biosynthesis ability between juveniles of Japanese flounder and common carp. Amino Acids 35: 161-168. DOI: 10.1007/s00726-007-0600-6.
Kim, S.K., Kim, K.G., Kim, K.D., Kim, K.W., Son, M.H., Rust, M., Johnson, R. 2014. Effect of dietary taurine levels on the conjugated bile acid composition and growth of juvenile Korean rockfish Sebastes schlegeli (Hilgendorf). Aquaculture Research 46: 2768-2775. DOI: 10.1111/are.12431.
Koven, W., Peduel, A., Gada, M., Nixon, O., Ucko, M. 2016. Taurine improves the performance of white grouper juveniles Epinephelus aeneus fed a reduced fish meal diet. Aquaculture 460: 8-14. DOI: 10.1016/j.aquaculture.2016.04.004.
Li, M., Lai, H., Li, Q., Gong, S., Wang, R. 2016. Effects of dietary taurine on growth, immunity and hyperammonemia in juvenile yellow catfish, Pelteobagrus fulvidraco fed all-plant protein diets. Aquaculture 450: 349-355. DOI: 10.1016/j.aquaculture.2015.08.013.
Maita, M., Maekawa, J., Satoh, K., Futami, K., Satoh, S. 2006. Disease resistance and hypocholesterolemia in yellowtail Seriola quinqueradiata fed a non-fishmeal diet. Fisheries Sciences 72: 513-519. DOI: 10.1111/j.1444-2906.2006.01179.x.
Matsunari, H., Yamamoto, T., Kim, S.K., Goto, T., Takeuchi, T. 2008. Optimum dietary taurine level in casein-based diet for juvenile red sea bream Pagrus major. Fisheries Science 74: 347-353. DOI: 10.1111/j.1444-2906.2008.01532.x.
Martins, N., Diógenes, A.F., Magalhães, R., Matas, I., Oliva-Teles, A., Peres, H. 2021. Dietary taurine supplementation affects lipid metabolism and improves the oxidative status of European seabass Dicentrarchus labrax juveniles. Aquaculture 531: 735820. DOI: 10.1016/j.aquaculture. 2020.735820.
Michelato, M., Furuya, W.M., Gatlin, D.M. 2018. Metabolic responses of Nile tilapia Oreochromis niloticus to methionine and taurine supplementation. Aquaculture 485: 66-72.  DOI: 10.1016/j.aquaculture.2017.11.003.
Nguyen, H.P., Van Do, T. 2021. Digested soybean protein and taurine influence bile acid level, lipase activity, lipid digestibility, and growth performance of pompano Trachinotus blochii. Fish Physiology and Biochemistry 47: 1199-1209. DOI: 10.1007/s10695-021-00972-3.
Peter, N., Pradhan, C., Dileep, N., Musharraf, M., Thazhakot Vasunambisan, S. 2022. Dietary taurine improved growth performance, nutrient utilization, and antioxidant enzyme activities in pangasius Pangasianodon hypophthalmus. Journal of the World Aquaculture Society 53: 106-121. DOI: 10.1111/jwas.12778.
Peter, N., Pradhan, C., Dileep, N., Vineetha, V.P., Das, S., Mohanta, K.N. 2025. Effect of dietary taurine along with the different lipid levels on growth, antioxidant, innate immune responses, digestive, metabolic enzyme activity and health status of pangasius Pangasianodon hypophthalmus. Aquaculture Science and Management 2: 1-10. DOI: 10.1186/s44365-025-00014-6.
Pourhosein Sarmeh, S. 2022. Application of various plant-based fat sources in sturgeon nutrition. Aquatic Animals Nutrition 8: 39-52. DOI: 10.22124/janb.2023.23773.1184.
Qi, G., Ai, Q., Mai, K., Xu, W., Liufu, Z., Yun, B., Zhou, H. 2012. Effects of dietary taurine supplementation to a casein-based diet on growth performance and taurine distribution in two sizes of juvenile turbot Scophthalmus maximus L. Aquaculture 358-359: 122-128. DOI: 10.1016/j. aquaculture.2012.06.018.
Ripps, H., Shen, W. 2012. Taurine: A very essential amino acid. Molecular Vision 18: 2673-2686.
Salman, A.S., Sultan, F.A. 2022. Effect of the amino acid taurine on some growth parameters of grass carp Ctenopharyngodon idella fingerlings. Basrah Journal of Agricultural Sciences 35: 291-301. DOI: 10.37077/25200860.2022.35.2.22.
Salze, G.P., Davis, D.A. 2015. Taurine: a critical nutrient for future fish feeds. Aquaculture 437: 215-229. DOI: 10.1016/j.aquaculture.2014.12.006
Salze, G.P., Spangler, E., Cobine, P.A., Rhodes, M., Davis, D.A. 2016. Investigation of biomarkers of early taurine deficiency in Florida pompano Trachinotus carolinus. Aquaculture 451: 254-265. DOI: 10.1016/j.aquaculture.2015.09.019.
Sampath, W.W.H.A., Rathnayake, R.M.D.S., Yang, M., Zhang, W., Mai, K. 2020. Roles of dietary taurine in fish nutrition. Marine Life Science and Technology 2: 360-375. DOI: 10.1007/s42995-020-00051-1.
Shen, G., Wang, S., Dong, J., Feng, J., Xu, J., Xia, F., Wang, X., Ye, J. 2019. Metabolic effect of dietary taurine supplementation on grouper Epinephelus coioides: a 1H-NMR-based metabolomics study. Molecules 24: 2253. DOI: 10.3390/molecules24122253.
Sundararajan, R., Bharampuram, A., Koduru, R. 2014. A review on phytoconstituents for nephroprotective activity. Pharmacophore 5: 160-182.
Tacon, A.G.J., Hasan, M.R., Subasinghe, R.P. 2006. Use of fishery resources as feed inputs for aquaculture development: trends and policy implications. FAO Fisheries Circular. No.1018. Rome, FAO. 99p.
Wang, X., Bai, F., Niu, X., Sun, Y., Ye, J. 2022. The lipid-lowering effect of dietary taurine in orange-spotted groupers Epinephelus coioides involves both bile acids and lipid metabolism. Frontiers in Marine Science 9: 859428. DOI: 10.3389/fmars.2022.859428.
Wu, G. 2010. Functional amino acids in growth, reproduction, and health. Advances in Nutrition 1: 31-37. DOI: 10.3945/an.110.1008.
Yun, B., Ai, Q., Mai, K., Xu, W., Qi, G., Luo, Y. 2012. Synergistic effects of dietary cholesterol and taurine on growth performance and cholesterol metabolism in juvenile turbot Scophthalmus maximus L. fed high plant protein diets. Aquaculture 324: 85-91. DOI: 10.1016/j. aquaculture.2011.10.012.
Zhang, J., Hu, Y., Ai, Q., Mao, P., Tian, Q., Zhong, L., Xiao, T., Chu, W. 2018. Effect of dietary taurine supplementation on growth performance, digestive enzyme activities and antioxidant status of juvenile black carp Mylopharyngodon piceus fed with low fish meal diet. Aquaculture Research 49: 3187-3195. DOI: 10.1111/are.13783.
Zhang, Y., Guo, F., Yang, X., Liu, Y., Bao, Y., Wang, Z., Hu, Z., Zhou, Q. 2023. Insights into the mechanism of growth and fat deposition by feeding different levels of lipid provided by transcriptome analysis of swamp eel (Monopterus albus, Zuiew 1793) liver. Frontiers in Immunology 14: 1118198. DOI: 10.3389/fimmu.2023.1118198.