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Sexual Dimorphism in Clinical Chemistry and Profile of Hybrid Catfish (Heterobranchus longifilis) | ||
Iranian Journal of Veterinary Science and Technology | ||
مقالات آماده انتشار، اصلاح شده برای چاپ، انتشار آنلاین از تاریخ 29 شهریور 1402 اصل مقاله (604.7 K) | ||
نوع مقاله: Research Article | ||
شناسه دیجیتال (DOI): 10.22067/ijvst.2023.80588.1221 | ||
نویسندگان | ||
POLYCARP NWUNUJI TANKO* 1؛ Garleya Bilbonga2؛ MICHAL MOLWAT SATI1 | ||
1Department of Veterinary Microbiology and Pathology, Faculty of Veterinary Medicine, University of Jos, Jos, Nigeria. | ||
2Department of Animal Production and Health. Faculty of Agriculture, Federal University Wukari, Wukari, Taraba State, Nigeria. | ||
چکیده | ||
Sex has been reported to influence the clinical chemistry of several species of fish. Whether sex impacts serum biochemistry composition and electrolyte profile of Heterobranchus longifilis is not well captured in the literature. This study aimed to evaluate the impact of sex on the clinical chemistry composition and electrolyte profile of hybrid catfish, Heterobranchus longifilis. Blood samples were collected and biochemically analyzed. The analytes analyzed included alanine aminotransferase, alkaline phosphatase, aspartate aminotransferase, creatinine, total bilirubin, conjugated bilirubin, unconjugated bilirubin, serum protein, albumin, total cholesterol, high-density lipoprotein, low-density lipoprotein, triglyceride, and urea. Uric acid, bicarbonate, Chloride, Sodium, and Potassium from 40 healthy Heterobranchus longifilis (20 males and 20 females). The males and females were not reproductively active at the time of sampling (None of the females had eggs). Most clinical chemistry analytes and electrolyte profiles of Heterobranchus longifilis showed differences between male and female values even though only a few (alanine aminotransferase, aspartate aminotransferase, creatinine, triglyceride, and uric acid) were statistically significant (p < 0.05). Based on the findings in this study, we suggest that sexual differences affect the clinical chemistry and electrolyte profile of Heterobranchus longifilis. Hence, sexual differences should be taken into consideration during sampling in both natural and experimental studies in Heterobranchus longifilis. | ||
کلیدواژهها | ||
Electrolytes؛ Heterobranchus longifilis؛ clinical chemistry؛ Sex | ||
مراجع | ||
1. Ahmed I, Sheikh ZA. Comparative study of hematological parameters of snow trout Schizopyge plagiostomus and Schizopyge niger inhabiting two different habitats. The European Zoological Journal. 2020;87(1):12-9.Doi: 10.1080/24750263.2019.1705647. 2. World Health Organization. The state of food security and nutrition in the world 2018: building climate resilience for food security and nutrition. Food & Agriculture Org. 2018 . 3. Ojutiku RO. comparative survival and growth rate of clarias gariepinus and heteroclarias hathclings fed live and frozen Daphnia. Pakistan Journal of Nutrition. 2008;7(4):527-9.Doi: 10.3923/pjn.2008.527.529. 4. Nadirah AN, Sabri MY, Emikpe BO, Noraini O, Tanko PN, Opeyemi OM, Ina-Salwany MY. The Effect of Heat Stress on the Oxidative Status of Red Hybrid Tilapia (Oreochromis sp.) Infected With Streptococcus Agalactiae. International Journal of Pharmaceutical Research & Allied Sciences. 2016 ;5(4). 5. Suleiman B, Adamu S, Abdullahi SA. Influence of sex on haematological and biochemical profiles of pond-reared Heterobranchus longifilis (Valenciennes, 1840). Nigerian J Fish Aquacult. 2016;4(1):28-33. 6. Offem BO, Ayotunde EO, Ikpi GU. Dynamics in the reproductive biology of Heterobranchus longifilis Val,(Pisces: 1840) in the inland wetlands of Cross River, Nigeria. Research journal of fisheries and Hydrobiology. 2008;3(1):22-31. 7. David M, Ramesh H, Patil VK, Marigoudar SR, Chebbi SG. Sodium cyanide-induced modulations in the activities of some oxidative enzymes and metabolites in the fingerlings of Cyprinus carpio (Linnaeus). Toxicological and Environ Chemistry. 2010;92(10):1841-9. 8. Ahmed I, Sheikh ZA. Comparative study of hematological parameters of snow trout Schizopyge plagiostomus and Schizopyge niger inhabiting two different habitats. The European Zoological Journal. 2020;87(1):12-9.Doi: 10.1080/24750263.2019.1705647. 9. Pradhan SC, Patra AK, Sarkar B, Pal A. Seasonal changes in hematological parameters of Catla catla (Hamilton 1822). Comparative Clinical Pathology. 2012;21(6):1473-81.Doi: 10.1007/s00580-011-1316-2. 10. Jan K, Ahmed I. The influence of sex and season on some hematological and biochemical parameters of snow trout Schizothorax labiatus in the Indian Himalayan Region. Fisheries Science. 2021;87(1):39-54. 10.1007/s12562-020-01469-3. 11. Jan K, Ahmed I, Dar NA. Haematological and serum biochemical reference values of snow trout, Schizothorax labiatus habiting in river Sindh of Indian Himalayan region. Journal of Fish Biology. 2021;98(5):1289-302.Doi: 10.1111/jfb.14661. 12. Ahmed I, Sheikh ZA, Wani GB, Shah BA. Sex variation in hematological and serum biochemical parameters of cultured Chinese silver carp, Hypophthalmichthys molitrix. Comparative Clinical Pathology. 2019;28(6):1761-7. 13. Zakęś Z, Demska-Zakęś K, Szczepkowski M, Rożyński M, Ziomek E. Impact of sex and diet on hematological and blood plasma biochemical profiles and liver histology of pikeperch (Sander lucioperca (L.)). Fisheries & Aquatic Life. 2016;24(2):61-8.Doi:10.1515/aopf-2016-007. 14. Kulkarni RS. Sex differences in the blood biochemical parameters of the fresh water fish, Notopterus notopterus (Pallas, 1789). World News of Natural Sciences. 2017;6. 15. Gabriel UU, Ezeri GN, Opabunmi OO. Influence of sex, source, health status and acclimation on the haematology of Clarias gariepinus (Burch, 1822). African Journal of Biotechnology. 2004;3(9):463-467. 16. Sheikh ZA, Ahmed I. Impact of environmental changes on plasma biochemistry and hematological parameters of Himalayan snow trout, Schizothorax plagiostomus. Comparative Clinical Pathology. 2019;28(3):793-804. Doi:10.1007/s00580-019-02914-1. 17. Charoo SQ, Chalkoo SR, Qureshi TA. Sexual differentiation in blood biochemistry of rainbow trout (Oncorhynchus mykiss). International Journal of Advanced Fisheries and Aquatic Science. 2013;1(1):32-8. 18. Abbas MW, Shamshad T, Ashraf MA, Javaid R. Jaundice: a basic review. Int J Res Med Sci. 2016;4(5):1313-9.Doi: 10.18203/2320-6012.ijrms20161196. 19. Tsai MT, Tarng DC. Beyond a measure of liver function—bilirubin acts as a potential cardiovascular protector in chronic kidney disease patients. International journal of molecular sciences. 2018;20(1):117.Doi: 10.3390/ijms20010117. 20. Suleiman, B. Organo-somatic indices of growth rate and sex categorised artificially spawned Heterobranchus longifilis Valenciennes, 1840. Biological and environmental sciences journal for the tropics. 2015;12:579-582. 21. Sharma NK, Akhtar MS, Pandey NN, Singh R, Singh AK. Sex specific seasonal variation in hematological and serum biochemical indices of Barilius bendelisis from Central Himalaya, India. Proceedings of the National Academy of Sciences, India Section B: Biological Sciences. 2017;87(4):1185-97.Doi: :10.1007/s40011-015-0692-9. 22. Knowles S, Hrubec TC, Smith SA, Bakal RS. Hematology and plasma chemistry reference intervals for cultured shortnose sturgeon (Acipenser brevirostrum). Veterinary Clinical Pathology. 2006;35(4):434-40.Doi: 10.1111/j.1939-165x.2006.tb00160.x. 23. Yousefian M, Sheikholeslami A, Kor Davood M. Serum biochemical parameter of male, immature and female Persian sturgeon (Acipencer persicus). Aust J Basic Appl Sci. 2011;5(5):476-81. 24. Baker DW, Wood AM, Litvak MK, Kieffer JD. Haematology of juvenile Acipenser oxyrinchus and Acipenser brevirostrum at rest and following forced activity. Journal of Fish Biology. 2005;66(1):208-21. 25. Giberson AV, Litvak MK. Effect of feeding frequency on growth, food conversion efficiency, and meal size of juvenile Atlantic sturgeon and shortnose sturgeon. North American Journal of Aquaculture. 2003;65(2):99-105.Doi: 10.1577/1548-8454(2003)65<99:EOFFOG>2.0.CO;2. 26. Wallaert C, Babin PJ. Age-related, sex-related, and seasonal changes of plasma lipoprotein concentrations in trout. Journal of lipid research. 1994;35(9):1619-33. 27. Cho KH. The Current Status of Research on High-Density Lipoproteins (HDL): A Paradigm Shift from HDL Quantity to HDL Quality and HDL Functionality. International Journal of Molecular Sciences. 2022;23(7):3967.Doi: 10.3390/ijms23073967. 28. Mohamed AS, El Desoky MA, Gad NS. The Changes in Triglyceride and Total Cholesterol Concentrations in the Liver and Muscle of Two Fish Species from Qarun Lake, Egypt. Organic & Medicinal Chemistry International Journal. 2019;9(4):86-90.Doi: 10.19080/OFOAJ.2019.09.555770. 29. Svoboda M, Kouřil J, Hamáčková J, Kalab P, Savina L, Svobodova Z, Vykusova B. Biochemical profile of blood plasma of tench (Tinca tinca L.) during pre-and postspawning period. Acta Veterinaria Brno. 2001;70(3):259-68.Doi: 10.2754/avb200170030259. 30. Ciereszko A, Dabrowski K, Kucharczyk D, Dobosz S, Goryczko K, Glogowski J. The presence of uric acid, an antioxidantive substance, in fish seminal plasma. Fish Physiology and Biochemistry. 1999;21(4):313-5. 31. Choi HK, Mount DB, Reginato AM. Pathogenesis of gout. Annals of internal medicine. 2005;143(7):499-516.Doi: 10.7326/0003-4819-143-7-200510040-00009. 32. Kavya KS, Jadesh M, Kulkarni RS. Hematology and serum biochemical changes in response to change in saline concentration in fresh water fish Notopterus notopterus. World Scientific News. 2016;32:36-47. | ||
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