The Impact of Seaweed-Derived Feed Additives (Aschomax) on Growth, Feed Utilization, Immunity, and Biochemical Profiles of Common Carp (Cyprinus carpio)
Yıl 2025,
Cilt: 8 Sayı: 2, 93 - 104, 31.12.2025
Arafat Ahmed
,
Khalidah S. Al-niaeem
,
Hayder A. H. Al-hasson
Öz
The overuse of antibiotics and synthetic feed additives in aquaculture involves risks to fish health and the environment. Finding natural alternatives to synthetic materials is critical for sustainable aquaculture enter-prises. The present study was conducted to investigate the effects of Seaweed-Derived Feed Additives (Aschomax) supplementation with different concentrations (0%, 1%, 2%, and 3%) on growth, feed utiliza-tion, immunological parameters, and blood biochemical indices of common carp (Cyprinus carpio) over a 60-day feeding period. The results demonstrated that growth performance parameters were significantly en-hanced in fish fed with 2% Aschomax supplementation. Moreover, immunological parameters were markedly improved across all Aschomax-supplemented groups, with the 2% inclusion level showing superior results. This was evidenced by significantly elevated levels of Myeloperoxidase (MOP: 0.59%), Nitroblue tetrazolium (NBT) activity (38.5%), and lysozyme activity (37.8 U/mL), indicating enhanced non-specific immune re-sponses. Furthermore, 2% of Aschomax demonstrated the most favorable lipid profile, characterized by re-duced total cholesterol (TC) (140.21 mg/100 ml) and triglycerides (TG) (75.23 mg/100 ml), alongside elevat-ed high-density lipoprotein (HDL) (93.60 mg/100 ml) and reduced low density lipoprotein (LDL) (50.54 mg/100 ml) levels. Notably, liver enzyme activities (ALP, ALT, and AST) remained unchanged across all treatments. These findings suggest that Aschomax supplementation at 2% effectively enhanced growth per-formance and stimulates the immune system of C. carpio. The alteration in blood biochemical parameters suggests improved metabolic efficiency and overall health status.
Etik Beyan
All applicable international, national, or institutional guidelines for the care and use of animals were followed. Ethical approval for this study (MSC119-2024), dated 01-September 2024 was obtained from the MSC Ethics Committee, Marine Science Center, University of Basrah, Iraq.
Destekleyen Kurum
This work was funded by the Marine Sci-ence Centre, the University of Basrah, Iraq.
Teşekkür
The authors would like to thank the agri-culture college for providing laboratory facilities and technical support.
Kaynakça
-
Abdel-Warith, A.-W. A., Younis, E.-S. M., Al-Asgah, N. A. (2016) Potential use of green macroalgae Ulva lactuca as a feed supplement in diets on growth performance, feed utilization and body composition of the African catfish, Clarias gariepinus. Saudi Journal of Biological Sciences, 23(3): 404-409.
-
Ahmed, A. R., Al-Hasson, H. A., Al-Niaeem, K. S. (2023) The effect of Shilajit on growth performance, blood parameters, and key liver enzymes of the common carp (Cyprinus carpio). Egyptian Journal of Aquatic Biology & Fisheries, 27(4).
-
Ahmed, A. R., Al-Zewar, J. M., Fawzi, N. A.-M., Abulhasan, A. A. (2020) Culture of common carp (Cyprinus carpio L.) in Basrah Governorate, southern Iraq; Current status and suggestions for development. Ecology, Environment and Conservation, 26(2): 824-831.
-
Ahmed, N., Sheikh, M. A., Ubaid, M., Chauhan, P., Kumar, K., Choudhary, S. (2024) Comprehensive exploration of marine algae diversity, bioactive compounds, health benefits, regulatory issues, and food and drug applications. Measurement: Food, 14:100163.
-
Alloyarova, Y. V., Kolotova, D. S., Derkach, S. R. (2024) Nutritional and therapeutic potential of functional components of brown seaweed: A review. Foods and Raw materials, 12(2): 398-419.
-
Al-Turaihi, Z., Ahmed, A., Al-Niaeem, K. (2023) Effect of dietary tinospora cordifolia supplementation on growth performance and hemato-biochemical parameters of the common carp (Cyprinus carpio). Egypt. J. Aquatic. Biol. Fish, 27(5): 677-688.
-
Amangelsin, Y., Semenova, Y., Dadar, M., Aljofan, M., Bjørklund, G. (2023) The impact of tetracycline pollution on the aquatic environment and removal strategies. Antibiotics, 12(3): 440.
-
AOAC, (2002) Official Methods of Analysis of Association of Official Analytical Chemists Association of Analytical Chemists, Arlington, VA, USA.
-
Ara, J., Sultana, V., Qasim, R., Ahmad, V. U. (2002) Hypolipidaemic activity of seaweed from Karachi coast. Phytotherapy Research: An International Journal Devoted to Pharmacological and Toxicological Evaluation of Natural Product Derivatives, 16(5): 479-483.
-
Ara, J., Sultana, V., Qasim, R., Ehteshamul‐Haque, S., Ahmad, V. U. (2005) Biological activity of Spatoglossum asperum: a brown alga. Phytotherapy Research: An International Journal Devoted to Pharmacological and Toxicological Evaluation of Natural Product Derivatives, 19(7): 618-623.
-
Aulia, D., Rivero, C., Choi, W., Hamidoghli, A., Bae, J., Hwang, S., Kim, D., Lee, S., Bai, S. (2024) Microalgae feed additives improve growth, immunity, and resistance to Vibrio anguillarum infection in juvenile rainbow trout, Oncorhynchus mykiss. Iranian Journal of Fisheries Sciences, 23(4): 537-557.
-
Biller-Takahashi, J., Takahashi, L., Saita, M., Gimbo, R., Urbinati, E. (2013) Leukocytes respiratory burst activity as indicator of innate immunity of pacu Piaractus mesopotamicus. Brazilian Journal of Biology, 73(2): 425-429.
-
Buchan, K. D., Prajsnar, T. K., Ogryzko, N. V., De Jong, N. W., Van Gent, M., Kolata, J., Foster, S. J., Van Strijp, J. A., Renshaw, S. A. (2019) A transgenic zebrafish line for in vivo visualisation of neutrophil myeloperoxidase. PLoS One, 14(4): e0215592.
-
Cheng, W., Yu, J.-S. (2013) Effects of the dietary administration of sodium alginate on the immune responses and disease resistance of Taiwan abalone, Haliotis diversicolor supertexta. Fish & shellfish immunology, 34(3): 902-908.
-
de Lima, J. S., Leão, A. D., de Jesus Oliveira, A. C., Chaves, L. L., Ramos, R. K. L. G., Rodrigues, C. F. C., Soares-Sobrinho, J. L., Soares, M. F. d. L. R. (2024) Potential of plant-based polysaccharides as therapeutic agents in ulcerogenic diseases of the gastrointestinal tract: A review. International Journal of Biological Macromolecules, 281: 136399.
-
FAO. (2020) World fisheries and aquaculture. Food and Agriculture Organization, 2020, 1-244.
-
Han, J., Balasubramanian, I., Flores, J. A., Bandyopadhyay, S., Yang, J., Liu, Y., Singh, R., Setty, P., Kiela, P., Ferraris, R. (2024) Intestinal lysozyme engagement of Salmonella Typhimurium stimulates the release of barrier-impairing InvE and Lpp1. Journal of Biological Chemistry, 300(7).
-
He, Y., Li, Y., Shen, P., Li, S., Zhang, L., Wang, Q., Ren, D., Liu, S., Zhang, D., Zhou, H. (2023) Anti-Hyperlipidemic Effect of Fucoidan Fractions Prepared from Iceland Brown Algae Ascophyllum nodosum in an Hyperlipidemic Mice Model. Marine Drugs, 21(9): 468.
-
Jiménez-Escrig, A., Sánchez-Muniz, F. (2000) Dietary fibre from edible seaweeds: Chemical structure, physicochemical properties and effects on cholesterol metabolism. Nutrition research, 20(4): 585-598.
-
Kamunde, C., Sappal, R., Melegy, T. M. (2019) Brown seaweed (AquaArom) supplementation increases food intake and improves growth, antioxidant status and resistance to temperature stress in Atlantic salmon, Salmo salar. PLoS One, 14(7): e0219792.
-
Leonard, S., Sweeney, T., Bahar, B., Lynch, B., O'doherty, J. (2011) Effects of dietary seaweed extract supplementation in sows and post-weaned pigs on performance, intestinal morphology, intestinal microflora and immune status. British journal of nutrition, 106(5): 688-699.
-
Li, Y., Zheng, Y., Zhang, Y., Yang, Y., Wang, P., Imre, B., Wong, A. C., Hsieh, Y. S., Wang, D. (2021) Brown algae carbohydrates: Structures, pharmaceutical properties, and research challenges. Marine Drugs, 19(11): 620.
-
Matin, M., Koszarska, M., Atanasov, A. G., Król-Szmajda, K., Jóźwik, A., Stelmasiak, A., Hejna, M. (2024) Bioactive potential of algae and algae-derived compounds: focus on anti-inflammatory, antimicrobial, and antioxidant effects. Molecules, 29(19): 4695.
-
Mohamed, A. S., Gad, N. S., El Desoky, M. A. (2019) Liver Enzyme Activity of Tilapia zillii and Mugil capito Collected Seasonally from Qarun Lake, Egypt. Fisheries and Aquaculture Journal, 10(1): 1-5.
-
Muahiddah, N., Diamahesa, W. A. (2022) Potential use of brown algae as an immunostimulant material in the aquaculture field to increase non-specific immunity and fight disease. Journal of Fish Health, 2(2): 109-115.
-
National Center for Health Statistics (NCHS). (2006) Abnormal lipid levels, diagnosed high cholesterol, and lipid-lowering treatment among adults: United States, 1999–2006. U.S. Department of Health and Human Services, Centers for Disease Control and Prevention.
-
National Cholesterol Education Program (NCEP). (1994) Second report of the expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (Adult Treatment Panel II). Circulation, 89(3): 1333–1445.
-
Nazarudin, M. F., Yusoff, F., Idrus, E. S., Aliyu-Paiko, M. (2020) Brown seaweed Sargassum polycystum as dietary supplement exhibits prebiotic potentials in Asian sea bass Lates calcarifer fingerlings. Aquaculture Reports, 18: 100488.
-
Pal, A., Kamthania, M. C., Kumar, A. (2014) Bioactive compounds and properties of seaweeds—a review. Open Access Library Journal, 1(4): 1-17.
-
Pham, M. A., Lee, K.-J., Lee, B.-J., Lim, S.-J., Kim, S.-S., Lee, Y.-D., Heo, M.-S., Lee, K.-W. (2006) Effects of dietary Hizikia fusiformis on growth and immune responses in juvenile olive flounder (Paralichthys olivaceus). Asian-australasian journal of animal sciences, 19(12): 1769-1775.
-
Quade, M. J., Roth, J. A. (1997) A rapid, direct assay to measure degranulation of bovine neutrophil primary granules. Veterinary immunology and immunopathology, 58(3-4): 239-248.
-
Ragaza, J. A., Koshio, S., Mamauag, R. E., Ishikawa, M., Yokoyama, S., Villamor, S. S. (2015) Dietary supplemental effects of red seaweed Eucheuma denticulatum on growth performance, carcass composition and blood chemistry of juvenile Japanese flounder, Paralichthys olivaceus. Aquaculture Research, 46(3): 647-657.
-
Remya, R., Samrot, A. V., Kumar, S. S., Mohanavel, V., Karthick, A., Chinnaiyan, V. K., Umapathy, D., Muhibbullah, M. (2022) Bioactive potential of brown algae. Adsorption science & technology, 2022, 9104835.
-
Samanta, P., Pal, S., Mukherjee, A. K., Ghosh, A. R. (2014) Evaluation of metabolic enzymes in response to Excel Mera 71, a glyphosate‐based herbicide, and recovery pattern in freshwater teleostean fishes. BioMed research international, 2014(1): 425159.
-
Sheikhzadeh, N., Ahmadifar, E., Soltani, M., Tayefi-Nasrabadi, H., Mousavi, S., Naiel, M. A. (2022) Brown seaweed (Padina australis) extract can promote performance, innate immune responses, digestive enzyme activities, intestinal gene expression and resistance against Aeromonas hydrophila in common carp (Cyprinus carpio). Animals, 12(23): 3389.
-
Shen, J., Liu, H., Wang, M., Lu, B., Ke, K., Wei, Y., Gao, F., Wang, Q., Huang, S., Ma, Y. (2025) Effects of Brown Algae (Laminaria japonica) Extract on Growth Performance, Immune Function and Intestinal Health of Largemouth Bass (Micropterus salmoides). Animals, 15(5): 622.
-
Shi, Q., Rong, H., Hao, M., Zhu, D., Aweya, J. J., Li, S., Wen, X. (2019) Effects of dietary Sargassum horneri on growth performance, serum biochemical parameters, hepatic antioxidant status, and immune responses of juvenile black sea bream Acanthopagrus schlegelii. Journal of Applied Phycology, 31(3): 2103-2113.
-
Siwicki, A. (1987), Immunomodulating activity of levamisole in carp spawners, Cyprinus carpio L.. Journal of Fish Biology, 31:245-246. https://doi.org/10.1111/j.1095-8649.1987.tb05325.x.
-
Siwicki, A. K., Anderson, D. P., Rumsey, G. L. (1994) Dietary intake of immunostimulants by rainbow trout affects non-specific immunity and protection against furunculosis. Veterinary immunology and immunopathology, 41(1-2): 125-139.
-
Thepot, V., Campbell, A. H., Paul, N. A., Rimmer, M. A. (2021). Seaweed dietary supplements enhance the innate immune response of the mottled rabbitfish, Siganus fuscescens. Fish & shellfish immunology, 113: 176-184.
-
UN. (2017) World Population Prospects: The 2017 Revision. United Nations, Department of Economic and Social Affairs. Retrieved 1 Jun 2025 from https://www.un.org/en/desa/world-population-projected-reach-98-billion-2050-and-112-billion-2100
-
Xie, M., Hao, Q., Olsen, R. E., Ringø, E., Yang, Y., Zhang, Z., Ran, C., & Zhou, Z. (2022) Growth performance, hepatic enzymes, and gut health status of common carp (Cyprinus carpio) in response to dietary Cetobacterium somerae fermentation product. Aquaculture Reports, 23: 101046.
-
Yang, F., Nagahawatta, D., Yang, H.-W., Ryu, B., Lee, H.-G., Je, J.-G., Heo, M.-S., Jeon, Y.-J. (2023) In vitro and in vivo immuno-enhancing effect of fucoidan isolated from non-edible brown seaweed Sargassum thunbergii. International Journal of Biological Macromolecules, 253: 127212.
-
Yang, Q., Yang, R., Li, M., Zhou, Q., Liang, X., Elmada, Z. C. (2014) Effects of dietary fucoidan on the blood constituents, anti-oxidation and innate immunity of juvenile yellow catfish (Pelteobagrus fulvidraco). Fish & shellfish immunology, 41(2): 264-270.
The Impact of Seaweed-Derived Feed Additives (Aschomax) on Growth, Feed Utilization, Immunity, and Biochemical Profiles of Common Carp (Cyprinus carpio)
Yıl 2025,
Cilt: 8 Sayı: 2, 93 - 104, 31.12.2025
Arafat Ahmed
,
Khalidah S. Al-niaeem
,
Hayder A. H. Al-hasson
Öz
The overuse of antibiotics and synthetic feed additives in aquaculture involves risks to fish health and the environment. Finding natural alternatives to synthetic materials is critical for sustainable aquaculture enter-prises. The present study was conducted to investigate the effects of Seaweed-Derived Feed Additives (Aschomax) supplementation with different concentrations (0%, 1%, 2%, and 3%) on growth, feed utiliza-tion, immunological parameters, and blood biochemical indices of common carp (Cyprinus carpio) over a 60-day feeding period. The results demonstrated that growth performance parameters were significantly en-hanced in fish fed with 2% Aschomax supplementation. Moreover, immunological parameters were markedly improved across all Aschomax-supplemented groups, with the 2% inclusion level showing superior results. This was evidenced by significantly elevated levels of Myeloperoxidase (MOP: 0.59%), Nitroblue tetrazolium (NBT) activity (38.5%), and lysozyme activity (37.8 U/mL), indicating enhanced non-specific immune re-sponses. Furthermore, 2% of Aschomax demonstrated the most favorable lipid profile, characterized by re-duced total cholesterol (TC) (140.21 mg/100 ml) and triglycerides (TG) (75.23 mg/100 ml), alongside elevat-ed high-density lipoprotein (HDL) (93.60 mg/100 ml) and reduced low density lipoprotein (LDL) (50.54 mg/100 ml) levels. Notably, liver enzyme activities (ALP, ALT, and AST) remained unchanged across all treatments. These findings suggest that Aschomax supplementation at 2% effectively enhanced growth per-formance and stimulates the immune system of C. carpio. The alteration in blood biochemical parameters suggests improved metabolic efficiency and overall health status.
Kaynakça
-
Abdel-Warith, A.-W. A., Younis, E.-S. M., Al-Asgah, N. A. (2016) Potential use of green macroalgae Ulva lactuca as a feed supplement in diets on growth performance, feed utilization and body composition of the African catfish, Clarias gariepinus. Saudi Journal of Biological Sciences, 23(3): 404-409.
-
Ahmed, A. R., Al-Hasson, H. A., Al-Niaeem, K. S. (2023) The effect of Shilajit on growth performance, blood parameters, and key liver enzymes of the common carp (Cyprinus carpio). Egyptian Journal of Aquatic Biology & Fisheries, 27(4).
-
Ahmed, A. R., Al-Zewar, J. M., Fawzi, N. A.-M., Abulhasan, A. A. (2020) Culture of common carp (Cyprinus carpio L.) in Basrah Governorate, southern Iraq; Current status and suggestions for development. Ecology, Environment and Conservation, 26(2): 824-831.
-
Ahmed, N., Sheikh, M. A., Ubaid, M., Chauhan, P., Kumar, K., Choudhary, S. (2024) Comprehensive exploration of marine algae diversity, bioactive compounds, health benefits, regulatory issues, and food and drug applications. Measurement: Food, 14:100163.
-
Alloyarova, Y. V., Kolotova, D. S., Derkach, S. R. (2024) Nutritional and therapeutic potential of functional components of brown seaweed: A review. Foods and Raw materials, 12(2): 398-419.
-
Al-Turaihi, Z., Ahmed, A., Al-Niaeem, K. (2023) Effect of dietary tinospora cordifolia supplementation on growth performance and hemato-biochemical parameters of the common carp (Cyprinus carpio). Egypt. J. Aquatic. Biol. Fish, 27(5): 677-688.
-
Amangelsin, Y., Semenova, Y., Dadar, M., Aljofan, M., Bjørklund, G. (2023) The impact of tetracycline pollution on the aquatic environment and removal strategies. Antibiotics, 12(3): 440.
-
AOAC, (2002) Official Methods of Analysis of Association of Official Analytical Chemists Association of Analytical Chemists, Arlington, VA, USA.
-
Ara, J., Sultana, V., Qasim, R., Ahmad, V. U. (2002) Hypolipidaemic activity of seaweed from Karachi coast. Phytotherapy Research: An International Journal Devoted to Pharmacological and Toxicological Evaluation of Natural Product Derivatives, 16(5): 479-483.
-
Ara, J., Sultana, V., Qasim, R., Ehteshamul‐Haque, S., Ahmad, V. U. (2005) Biological activity of Spatoglossum asperum: a brown alga. Phytotherapy Research: An International Journal Devoted to Pharmacological and Toxicological Evaluation of Natural Product Derivatives, 19(7): 618-623.
-
Aulia, D., Rivero, C., Choi, W., Hamidoghli, A., Bae, J., Hwang, S., Kim, D., Lee, S., Bai, S. (2024) Microalgae feed additives improve growth, immunity, and resistance to Vibrio anguillarum infection in juvenile rainbow trout, Oncorhynchus mykiss. Iranian Journal of Fisheries Sciences, 23(4): 537-557.
-
Biller-Takahashi, J., Takahashi, L., Saita, M., Gimbo, R., Urbinati, E. (2013) Leukocytes respiratory burst activity as indicator of innate immunity of pacu Piaractus mesopotamicus. Brazilian Journal of Biology, 73(2): 425-429.
-
Buchan, K. D., Prajsnar, T. K., Ogryzko, N. V., De Jong, N. W., Van Gent, M., Kolata, J., Foster, S. J., Van Strijp, J. A., Renshaw, S. A. (2019) A transgenic zebrafish line for in vivo visualisation of neutrophil myeloperoxidase. PLoS One, 14(4): e0215592.
-
Cheng, W., Yu, J.-S. (2013) Effects of the dietary administration of sodium alginate on the immune responses and disease resistance of Taiwan abalone, Haliotis diversicolor supertexta. Fish & shellfish immunology, 34(3): 902-908.
-
de Lima, J. S., Leão, A. D., de Jesus Oliveira, A. C., Chaves, L. L., Ramos, R. K. L. G., Rodrigues, C. F. C., Soares-Sobrinho, J. L., Soares, M. F. d. L. R. (2024) Potential of plant-based polysaccharides as therapeutic agents in ulcerogenic diseases of the gastrointestinal tract: A review. International Journal of Biological Macromolecules, 281: 136399.
-
FAO. (2020) World fisheries and aquaculture. Food and Agriculture Organization, 2020, 1-244.
-
Han, J., Balasubramanian, I., Flores, J. A., Bandyopadhyay, S., Yang, J., Liu, Y., Singh, R., Setty, P., Kiela, P., Ferraris, R. (2024) Intestinal lysozyme engagement of Salmonella Typhimurium stimulates the release of barrier-impairing InvE and Lpp1. Journal of Biological Chemistry, 300(7).
-
He, Y., Li, Y., Shen, P., Li, S., Zhang, L., Wang, Q., Ren, D., Liu, S., Zhang, D., Zhou, H. (2023) Anti-Hyperlipidemic Effect of Fucoidan Fractions Prepared from Iceland Brown Algae Ascophyllum nodosum in an Hyperlipidemic Mice Model. Marine Drugs, 21(9): 468.
-
Jiménez-Escrig, A., Sánchez-Muniz, F. (2000) Dietary fibre from edible seaweeds: Chemical structure, physicochemical properties and effects on cholesterol metabolism. Nutrition research, 20(4): 585-598.
-
Kamunde, C., Sappal, R., Melegy, T. M. (2019) Brown seaweed (AquaArom) supplementation increases food intake and improves growth, antioxidant status and resistance to temperature stress in Atlantic salmon, Salmo salar. PLoS One, 14(7): e0219792.
-
Leonard, S., Sweeney, T., Bahar, B., Lynch, B., O'doherty, J. (2011) Effects of dietary seaweed extract supplementation in sows and post-weaned pigs on performance, intestinal morphology, intestinal microflora and immune status. British journal of nutrition, 106(5): 688-699.
-
Li, Y., Zheng, Y., Zhang, Y., Yang, Y., Wang, P., Imre, B., Wong, A. C., Hsieh, Y. S., Wang, D. (2021) Brown algae carbohydrates: Structures, pharmaceutical properties, and research challenges. Marine Drugs, 19(11): 620.
-
Matin, M., Koszarska, M., Atanasov, A. G., Król-Szmajda, K., Jóźwik, A., Stelmasiak, A., Hejna, M. (2024) Bioactive potential of algae and algae-derived compounds: focus on anti-inflammatory, antimicrobial, and antioxidant effects. Molecules, 29(19): 4695.
-
Mohamed, A. S., Gad, N. S., El Desoky, M. A. (2019) Liver Enzyme Activity of Tilapia zillii and Mugil capito Collected Seasonally from Qarun Lake, Egypt. Fisheries and Aquaculture Journal, 10(1): 1-5.
-
Muahiddah, N., Diamahesa, W. A. (2022) Potential use of brown algae as an immunostimulant material in the aquaculture field to increase non-specific immunity and fight disease. Journal of Fish Health, 2(2): 109-115.
-
National Center for Health Statistics (NCHS). (2006) Abnormal lipid levels, diagnosed high cholesterol, and lipid-lowering treatment among adults: United States, 1999–2006. U.S. Department of Health and Human Services, Centers for Disease Control and Prevention.
-
National Cholesterol Education Program (NCEP). (1994) Second report of the expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (Adult Treatment Panel II). Circulation, 89(3): 1333–1445.
-
Nazarudin, M. F., Yusoff, F., Idrus, E. S., Aliyu-Paiko, M. (2020) Brown seaweed Sargassum polycystum as dietary supplement exhibits prebiotic potentials in Asian sea bass Lates calcarifer fingerlings. Aquaculture Reports, 18: 100488.
-
Pal, A., Kamthania, M. C., Kumar, A. (2014) Bioactive compounds and properties of seaweeds—a review. Open Access Library Journal, 1(4): 1-17.
-
Pham, M. A., Lee, K.-J., Lee, B.-J., Lim, S.-J., Kim, S.-S., Lee, Y.-D., Heo, M.-S., Lee, K.-W. (2006) Effects of dietary Hizikia fusiformis on growth and immune responses in juvenile olive flounder (Paralichthys olivaceus). Asian-australasian journal of animal sciences, 19(12): 1769-1775.
-
Quade, M. J., Roth, J. A. (1997) A rapid, direct assay to measure degranulation of bovine neutrophil primary granules. Veterinary immunology and immunopathology, 58(3-4): 239-248.
-
Ragaza, J. A., Koshio, S., Mamauag, R. E., Ishikawa, M., Yokoyama, S., Villamor, S. S. (2015) Dietary supplemental effects of red seaweed Eucheuma denticulatum on growth performance, carcass composition and blood chemistry of juvenile Japanese flounder, Paralichthys olivaceus. Aquaculture Research, 46(3): 647-657.
-
Remya, R., Samrot, A. V., Kumar, S. S., Mohanavel, V., Karthick, A., Chinnaiyan, V. K., Umapathy, D., Muhibbullah, M. (2022) Bioactive potential of brown algae. Adsorption science & technology, 2022, 9104835.
-
Samanta, P., Pal, S., Mukherjee, A. K., Ghosh, A. R. (2014) Evaluation of metabolic enzymes in response to Excel Mera 71, a glyphosate‐based herbicide, and recovery pattern in freshwater teleostean fishes. BioMed research international, 2014(1): 425159.
-
Sheikhzadeh, N., Ahmadifar, E., Soltani, M., Tayefi-Nasrabadi, H., Mousavi, S., Naiel, M. A. (2022) Brown seaweed (Padina australis) extract can promote performance, innate immune responses, digestive enzyme activities, intestinal gene expression and resistance against Aeromonas hydrophila in common carp (Cyprinus carpio). Animals, 12(23): 3389.
-
Shen, J., Liu, H., Wang, M., Lu, B., Ke, K., Wei, Y., Gao, F., Wang, Q., Huang, S., Ma, Y. (2025) Effects of Brown Algae (Laminaria japonica) Extract on Growth Performance, Immune Function and Intestinal Health of Largemouth Bass (Micropterus salmoides). Animals, 15(5): 622.
-
Shi, Q., Rong, H., Hao, M., Zhu, D., Aweya, J. J., Li, S., Wen, X. (2019) Effects of dietary Sargassum horneri on growth performance, serum biochemical parameters, hepatic antioxidant status, and immune responses of juvenile black sea bream Acanthopagrus schlegelii. Journal of Applied Phycology, 31(3): 2103-2113.
-
Siwicki, A. (1987), Immunomodulating activity of levamisole in carp spawners, Cyprinus carpio L.. Journal of Fish Biology, 31:245-246. https://doi.org/10.1111/j.1095-8649.1987.tb05325.x.
-
Siwicki, A. K., Anderson, D. P., Rumsey, G. L. (1994) Dietary intake of immunostimulants by rainbow trout affects non-specific immunity and protection against furunculosis. Veterinary immunology and immunopathology, 41(1-2): 125-139.
-
Thepot, V., Campbell, A. H., Paul, N. A., Rimmer, M. A. (2021). Seaweed dietary supplements enhance the innate immune response of the mottled rabbitfish, Siganus fuscescens. Fish & shellfish immunology, 113: 176-184.
-
UN. (2017) World Population Prospects: The 2017 Revision. United Nations, Department of Economic and Social Affairs. Retrieved 1 Jun 2025 from https://www.un.org/en/desa/world-population-projected-reach-98-billion-2050-and-112-billion-2100
-
Xie, M., Hao, Q., Olsen, R. E., Ringø, E., Yang, Y., Zhang, Z., Ran, C., & Zhou, Z. (2022) Growth performance, hepatic enzymes, and gut health status of common carp (Cyprinus carpio) in response to dietary Cetobacterium somerae fermentation product. Aquaculture Reports, 23: 101046.
-
Yang, F., Nagahawatta, D., Yang, H.-W., Ryu, B., Lee, H.-G., Je, J.-G., Heo, M.-S., Jeon, Y.-J. (2023) In vitro and in vivo immuno-enhancing effect of fucoidan isolated from non-edible brown seaweed Sargassum thunbergii. International Journal of Biological Macromolecules, 253: 127212.
-
Yang, Q., Yang, R., Li, M., Zhou, Q., Liang, X., Elmada, Z. C. (2014) Effects of dietary fucoidan on the blood constituents, anti-oxidation and innate immunity of juvenile yellow catfish (Pelteobagrus fulvidraco). Fish & shellfish immunology, 41(2): 264-270.