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Razavi Amria, Seyede Rahime, Gholipour Kanani, Hosna, Farhangi, Mohammad, Adineh, Hosein. (1403). The Effects of Phytobiotic-Enriched Diet on Immunity Index and Hematological-Biochemical Changes in Common Carp Fish (Cyprinus carpio). سامانه مدیریت نشریات علمی, 13(2), 381-390. doi: 10.22034/jmpb.2023.362144.1551
Seyede Rahime Razavi Amria; Hosna Gholipour Kanani; Mohammad Farhangi; Hosein Adineh. "The Effects of Phytobiotic-Enriched Diet on Immunity Index and Hematological-Biochemical Changes in Common Carp Fish (Cyprinus carpio)". سامانه مدیریت نشریات علمی, 13, 2, 1403, 381-390. doi: 10.22034/jmpb.2023.362144.1551
Razavi Amria, Seyede Rahime, Gholipour Kanani, Hosna, Farhangi, Mohammad, Adineh, Hosein. (1403). 'The Effects of Phytobiotic-Enriched Diet on Immunity Index and Hematological-Biochemical Changes in Common Carp Fish (Cyprinus carpio)', سامانه مدیریت نشریات علمی, 13(2), pp. 381-390. doi: 10.22034/jmpb.2023.362144.1551
Razavi Amria, Seyede Rahime, Gholipour Kanani, Hosna, Farhangi, Mohammad, Adineh, Hosein. The Effects of Phytobiotic-Enriched Diet on Immunity Index and Hematological-Biochemical Changes in Common Carp Fish (Cyprinus carpio). سامانه مدیریت نشریات علمی, 1403; 13(2): 381-390. doi: 10.22034/jmpb.2023.362144.1551

The Effects of Phytobiotic-Enriched Diet on Immunity Index and Hematological-Biochemical Changes in Common Carp Fish (Cyprinus carpio)

Journal of Medicinal plants and By-products
مقاله 13، دوره 13، شماره 2، شهریور 2024، صفحه 381-390    اصل مقاله (880.19 K)
نوع مقاله: Research Paper
شناسه دیجیتال (DOI): 10.22034/jmpb.2023.362144.1551
نویسندگان
Seyede Rahime Razavi Amria؛ Hosna Gholipour Kanani؛ Mohammad Farhangi* ؛ Hosein Adineh
Department of Fisheries, Faculty of Agriculture and Natural Resources, Gonbad Kavous University, Gonbad Kavous, Golestan, Iran
چکیده
The present study compared the effects of four medicinal herbs on the growth, digestive enzyme activity, innate immunity, and oxidative status of common carp juveniles (Cyprinus carpio). The juvenile fish (average weight: 80.01 ± 0.34 g) were fed with four diets, including 1% Zataria multiflora oil (T2), Zingiber powder (T3), garlic essential oil extract (T4), garlic peel extract (T5), and control diet (T1) without any additives, for seven weeks (20 individuals per replicate). The results showed that weight gain and specific growth rate were highest in the treatment fed with garlic and ginger extracts (T3 and T4). The protease and lipase activities in the medicinal herb treatments (especially the garlic extract treatment; T4) were significantly higher than in the control. Fish fed with medicinal herb-supplemented diets (except for Z. multiflora oil; T2) also displayed higher levels of serum lysozyme, alternative complement, total immunoglobulin, superoxide dismutase, and total protein levels compared to the control diet. The highest levels were observed at the 1% level of Zingiber powder (T3) and garlic extract (T4). Medicinal herb supplementation at a level of 1% is a natural immunostimulant and growth promoter supplement recommended for common carp.
کلیدواژه‌ها
Cyprinus carpio؛ Medicinal plants؛ Nutrition؛ Health
مراجع
  1. Rahman M.M. Role of common carp (Cyprinus carpio) in aquaculture production system. Frontiers in Life Science. 2015; 8: 399-410.
  2. Ghasemi Pirbalouti A. Iranian medicinal and aromatic plants (2nd edition). Islamic Azad University Publishers, Shahrekord, Iran. (In Persian). 238p; 2009.
  3. Citarasu T., Sivaram V., Immanuel G., Rout N., Murugan V. Influence of selected Indian immunostimulants herbs against white spot syndrome virus (WSSV) infection in black tiger shrimp, Penaeus monodon with reference to Haematological, biochemical and immunological changes. Fish and Shellfish Immunology. 2006; 21: 372–384.
  4. Adineh H., Harsij M., Jafaryan H., Asadi M. The effects of microencapsulated garlic (Allium sativum) extract on growth performance, body composition, immune response and antioxidant status of rainbow trout (Oncorhynchus mykiss) juveniles. Journal of Applied Animal Research. 2020; 48: 372-378.
  5. Jabran A.G., Soeharto S., Sujuti H. The effect of ginger (Zingiber officinale Roscoe) extract on liver histopathology and alanine aminotransferase serum level in carbofuran-induced rats. International J Pharm Tech Research. 2015; 8: 889- 897.
  6. Ramezani M., Hosseinzadeh H., Samizadeh S. Antnociceptive effects of Zataria multiflora Boiss fractions in mice. J Ethnopharmacology. 2015; 91: 167-170.
  7. Sepavand A., Ashraf Jafari A., Sefidkon F., Kalatejari S. Evaluation of growth, essential oil content and composition in four thyme species under dryland farming system in Zagheh, Rangeland, Khoramabad, Iran. J Medicinal Plants and By-products. 2021; 1: 59-65.
  8. Buchmann K. Evolution of innate immunity: clues from invertebrates via fish to mammals. Frontiers in Immunology. 2014; 5: 459.
  9. Dadgar SH, Seidgar M., Nekuiefard A., Valipour A.R., Sharifian M., Hafezieh M. Oral administration of garlic powder (Allium sativum) on growth performance and survival rate of Carassius auratus fingerlings. Iranian J Fisheries Sci. 2019; 18: 71-82
  10. Labrador J.R.P., Guinares R.C., Hontiveros GJS. Effect of garlic powder supplemented diets on the growth and survival of Pacific white leg shrimp (Litopenaeus vannamei). Cogent Food Agriculture. 2016; 2: 295-299.
  11. Lokesh B., Neeraja T., Haribabu P., Ramalingaiah D., Pamanna D. Effect of garlic supplemented diets on the growth and survival of Pacific white leg shrimp (Litopenaeus vannamei) Juveniles. J Entomology and Zoology Studies. 2020; 8: 295-299.
  12. Tanekhy M., Fall J. Expression of innate immunity genes in kuruma shrimp Marsupenaeus japonicus was studied after in vivo stimulation with garlic extract (allicin). Veterinarni Medicina. 2015; 60: 39–47.
  13. Chitsaz H., Oraji H., Keramat Amirkolaie H.A., Akrami A. Effect of garlic peel on haematological, biochemical and digestive enzyme activity in beluga juvenile (Huso huso). Iranian J Aquatic Animal Health. 2018; 4: 13-28.
  14. Kesbic O.S, Acar U., Hassaan M.S, Yılmaz, S, Guerrera, M.C, Fazio F. Effects of Tomato Paste by-product extract on growth performance and blood parameters in common carp (Cyprinus carpio). Animal. 2022; 12: 3387.
  15. Ngugi C.C., Oyoo-Okoth E., Mugo-Bundi J., Orina P.S., Chemoiwa E.J., Aloo P.A. Effects of dietary administration of stinging nettle (Urtica dioica) on the growth performance, biochemical, hematological and immunological parameters in juvenile and adult Victoria Labeo (Labeo victorianus) challenged with Aeromonas hydrophila. Fish and Shellfish Immunology. 2015; 44: 533–541.
  16. Fazelan Z., Vatnikov Y.A., Kulikov E.V., Plushikov V.G., Yousefi M. Effects of dietary ginger (Zingiber officinale) administration on growth performance and stress, immunological, and antioxidant responses of common carp (Cyprinus carpio) reared under high stocking density. Aquaculture. 2020; 518: 734833.
  17. Yousefi M., Zahedi S., Reverter M., Adineh H., Hoseini S.M., Van Doan H., Hoseinifar S.H. Enhanced growth performance, oxidative capacity and immune responses of common carp, Cyprinus carpio fed with Artemisia absinthium extract-supplemented diet. Aquaculture. 2020; 545: 737167.
  18. Lee D.H., Lim S.R., Han J.J., Lee S.W., Ra C.S., Kim J.D. Effect of dietary Garlic powder on growth, feed utilization and whole body composition changes in fingerling starlet sturgeon, Acipenser ruthenus. Asian-Australasian Journal of Animal Sciences. 2014; 27: 1303-1310.
  19. Adineh H., Naderi M., Hamidi M.K., Harsij M. Biofloc technology improves growth, innate immune responses, oxidative status, and resistance to acute stress in common carp (Cyprinus carpio) under high stocking density. Fish and shellfish immunology. 2019; 95: 440-448.
  20. Arabshahi-Delouee M., Asna Urooj S. Antioxidant properties of various solvent extracts of mulberry (Morus indica L.) leaves Author links open overlay panel. Food Chemistry. 2007; 102: 1233-1240.
  21. Eloff J.N. Which extractant should be used for the screening and isolation of antimicrobial components from plants? Journal of Ethno pharmacology. 1998; 6: 1-8.
  22. AOAC. Official Methods of Analysis, Association of Official Analytical Chemists International, Gaithersburg, 2005.
  23. Chang Y. P., Liu C.H., Wu C.C., Chiang C.M., Lian J.L., Hsieh S.L. Fish Dietary administration of zingerone to enhance growth, non-specific immune response, and resistance to Vibrio alginolyticus in pacific white shrimp (Litopenaeus vannamei) juvenles. Fish and Shell fish Immunology. 2012; 32: 284-290.
  24. Ahmadifard N., Abedian Kenari A., Motamedzadegan A. Study of Proteases (Gastric, Intestine and Pancreas) Enzyme Activities of Rainbow Trout, Oncorhynchus mykiss, fed partial substitution of dietary fish meal with rice bran protein concentrate. Journal of Fisheries-Iranian. 2012; 65: 365-376.
  25. Najdegerami E.H., Bakhshi F., Lakani F.B. Effects of biofloc on growth performance, digestive enzyme activities and liver histology of common carp (Cyprinus carpio L.) fingerlings in zero-water exchange system. Fish physiology and biochemistry. 2016; 42: 457-465.
  26. Langlois A., Corring T., Fevrier C. Effects of wheat bran on exocrine pancreas secretion in the pig. Reproduction Nutrition Developpement. 1987; 27: 929-939.
  27. Walter H. Proteinase's methods with hemoglobin, casein and azocoll as substrates. In: H. U. Bergmeyer (ed.), Methods of enzymatic analysis, 1984.
  28. Iijima N., Tanaka S., Ota Y. Purification and characterization of bile salt-activated lipase from the hepatopancreas of red sea bream, Pagrus major. Fish Physiology and Biochemistry. 1998; 18: 59-69.
  29. Ellis A. Lysozyme assay in techniques in fish immunology, SOS Publications, Fair Haven, NJ, USA, 1990.
  30. Siwicki A.K., Anderson D.P. Nonspecific defense mechanisms assay in fish. II. Potential killing activity of neutrophils and macrophages, lysozyme activity in serum and organs and total immunoglobulin (Ig) level in serum. In: Fish diseases diagnosis and preventions methods, Siwicki A.K., Anderson D.P., Waluga J. (eds). Wydawnictwo Instytutu Rybactwa Śródlądowego. 1993: 105-111.
  31. Sunyer A., Tort E. Natural hemolytic and bactericidal activities of sea bream Sparus aurata serum are effected by the alternative complement pathway. Veterinary Immunology and Immunopathology. 1995; 45: 333-345.
  32. Fridovich I. Superoxide radical and superoxide dismutases. Annual Review of Biochemistry. 1995; 64; 97-112.
  33. Beutler E. Red cell metabolism, a manual of biochemical methods. Grune and Straton Press, New York, 1975.
  34. Lowry O.H., Rosenbrough W.J., Fair H.L., Randall R.J. Protein measurement with folin phenol reagent. Journal of Biological Chemistry. 1951; 19: 265- 275.
  35. Thanikachalam K., Kasi M., Rathinam X. Effect of garlic peel on growth, hematological parameters and disease resistance against Aeromonas hydrophila in African catfish Clarias gariepinus (Bloch) fingerlings. Asian Pacific Journal of Tropical Medicine. 2016; 3: 614-618.
  36. Wang A., Meng X., Lub R., Wu C., Luo Y.T., Yan X., Li X.J., Kong X.A., Nie G.X. Effects of Rehmannia glutinosa on growth performance, immunological parameters and disease resistance to Aeromonas hydrophila in common carp (Cyprinus carpio L.). Aquaculture. 2015; 435: 293-300.
  37. Norhan E., SalehFady R., Michael M., Toutou R. Evaluation of garlic and onion powder as phyto-additives in the diet of sea bass (Dicentrarcus labrax). The Egyptian Journal Aquatic Research. 2015; 41: 211-217.
  38. Ndong J.D., Fall J. The effect of garlic (Allium sativum) on growth and immune responses of hybrid tilapia (Oreochromis niloticus×Oreochromis aureus). Journal of Clinical Immnunol and Immunopathology Research. 2011; 3: 1-9.
  39. Frankic T., Voljc M., Salobir Rezar V. Use of herbs and spices and their extracts in animal nutrition. Acta agriculturae Slovenica. 2009; 94: 95-102.
  40. Sankar S., Philip B., Philip R., Singh I.S.B. Effect of probiotics on digestive enzyme activities and growth of cichlids, Etroplus suratenis (Pearl spot) and Oreochromis mossambicus (Tilapia). Aquaculture Nutririon Journal. 2007; 23: 852-864.
  41. Jang I.S., Ko Y.H., Kang S.Y., Lee C.Y. Effects of a commercial essential oil on growth performance, digestive enzyme activity and intestinal microflora population in broiler chickens. Animal Feed Science and Technology. 2007; 134: 304-315.
  42. Boehm T. Evolution of vertebrate immunity. Current Biology. 2012; 22: 722-732.
  43. Meng X., Cai H., Li H., You F., Jiang A., Hu W., Zhou Z. Clostridium butyricum-fermented Chinese herbal medicine enhances the immunity by modulating the intestinal microflora of largemouth bass (Micropterus salmoides). Aquaculture. 2023; 562: 738768.
  44. Valenzuela-Gutiérrez R., Lago-Lestón A., Vargas-Albores F., Cicala F., Martínez-Porchas M. Exploring the garlic (Allium sativum) properties for fish aquaculture. Fish Physiology and Biochemistry. 2012; 47:1179-1198.
  45. Yilmaz S., Ergün S. Effects of garlic and ginger oils on hematological and biochemical parameters of sea bass, Dicentrarchus labrax. Journal Aquatic Animal Health. 2012; 24: 219-224.
  46. Immanuel G., Uma R.P., Iyapparay P., Citarasu T., Punitha S.M., Peter M., Michael B., Palavesam A. Dietary medicinal plant extracts improve growth, immune-activity and survival of tilapia Oreochromis mosssambicus. Journal of Fish Biology. 2009; 74: 1462.
  47. Shalaby A. M., Khattab Y.A., Abdel Rahman A.M. Effects of garlic (Allium sativum) and chloramphenicol on growth performance, physiological parameters and survival of Nile Tilapia immunostimulants for fish. Journal of Ethnopharmacology. 2006; 88: 99-106.
  48. Binaii M., Ghiasi M., Farabi S.M., Pourgholam R., Fazli H., Safari R., Alavi S.E., Taghavi M.J., Bankehsaz Z. Biochemical and haemato-immunological parameters in juvenile beluga (Huso huso) following the diet supplemented with nettle (Urtica dioica). Fish Shellfish Immunology. 2014; 36: 46-51.
  49. Christybapita D., Divyagnaneswari M., Michael R.D. Oral administration of Eclipta alba leaf aqueous extract enhances the non-specific immune responses and disease resistance of Oreochromis mossambicus. Fish and Shellfish Immunology. 2007; 4:840-852.
  50. Sarhadi I., Alizadeh E., Ahmadifar E., Adineh H., Dawood M.A. Skin Mucosal, Serum Immunity and Antioxidant Capacity of Common Carp (Cyprinus sp.) Fed Artemisia (Artemisia annua). Annals of Animal Science. 2020; 20: 1011-1027.
  51. Magnadóttir B. Innate immunity of fish (overview). Fish and Shell fish Immunology. 2006; 20: 37–151.
  52. Biller-Takahashi J.D., Takahashi L., Saita M., Gimbo R.Y., Urbinati E.C. Leukocytes respiratory burst activity as indicator of innate immunity of pacu Piaractus mesopotamicus. Brazi Journal Biology. 2013; 73: 425-429.
  53. He J., Qiang J., Gabriel N.N., Xu P., Yang R. Effect of feeding-intensity stress on biochemical and hematological indices of GIFT tilapia, Oreochromis niloticus. Turkish Journal of Fisheries and Aquatic Sciences. 2015; 15: 305-312.
  54. Livingstone D.R. Contaminant-stimulated reactive oxygen species production and oxidative damage in aquatic organisms. Marine Pollution Bulletin. 2001; 42: 656-666.
  55. Ritola O., Tossavainen K., Kiuru T., Lindstorm-Seppa P., Molsa H. Effect of continuous and episodic hyperoxia on stress and hepatic glutathione levels in one-summer old rainbow trout, Oncorhynchus mykiss. Journal of Applied Ichthyology. 2002; 18: 159-164.
  56. Manno M., Bertazzon A., Burlina A., Galzigna L. Interaction of low doses of ionizing radiation and carbon tetrachloride on liver superoxide dismutase and glutathione peroxidase in mice. Enzyme. 1985; 34: 107-112.
  57. Metwally M.A.A. Effects of garlic, Allium sativum on some antioxidant activities in Tilapia, Oreochromis niloticus. Fisheries Marine Science Journal. 2009; 1: 56-64.
  58. Islam M.N., Amel M. El., Amany A.A. Influence of dietary ginger (Zingiber officinale) on haemato-biochemical parameters, spleen histology and resistance of Oreochromis niloticus fingerlings to Aeromonas hydrophila infection. Egypt Journal of Aquatic. 2016; 6: 25-45.
  59. Saha N.A., Usami T., Suzuki Y. Seasonal changes in the immune activities of common carp (Cyprinus carpio). Fish Physiology and Biochemistry. 2002; 26: 379-38.
  60. Ahmadifar E., Hoseinifar S.H., Adineh H., Moghadam M.S., Dawood M.A. Assessing the impact of purslane (Portulaca oleracea L.) on growth performance, anti-oxidative, and immune activities in grass carp (Ctenopharyngodon idella). Annals of Animal Science. 2020; 20: 1427-1440.
  61. Yagi K. Assay for plasma lipid peroxidase. Methods in Enzymology. 1984; 109: 328-331.
  62. Giannenas I., El-Triantafillou S., Stavrakakis M., Margroni S., Mavridis T., Steiner E. Assessment of dietary supplementation with carvacrol or thymol containing feed additives on performance, intestinal microbiota and antioxidant status of rainbow trout (Oncorhynchus mykiss). Aquaculture. 2012; 350-353.
  63. Jafarinejad R., Gharaei A., Mirdar Harijani J. Dietary ginger improve growth performance, blood parameters, antioxidant capacity and gene expression in Cyprinus carpio. Iranian Journal of Fisheries Sciences. 2020; 19: 1237-1252.
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