Document Type : Article
Authors
1 Department of Fisheries Science, Faculty of Natural Resources, University of Kurdistan-Sanandaj
2 Assistant Professor, Department of Fisheries Science, Faculty of Natural Resources, University of Kurdistan, P.O. Box 416, Sanandaj, Iran
Abstract
In this study, the effects of genistein and 17β-estradiol (E2) was investigated on some semen seminal plasma biochemical and enzymes in male gibel carp, during the spermiation phase. Mature male gibel carp (with ~ 30 to 40 g body weight (BW)) received intramuscular injections of one of two genistein doses (5 μg/g BW; G5, or 50 μg/g BW; G50), (10 μg/g BW 17β-estradiol, E2), 10 μg/g BW corn oil+ DMSO .Then, milt were collected in order to measure seminal plasma ionic, nonionic compounds and enzymes. The results of this study showed, there were significant differences in seminal plasma ionic, nonionic compounds and enzymes among the treated groups (p
Keywords
Alavi, SMH.; Cosson, J. (2005). Sperm motility in fishes: Effects of temperature and pH: a review. Cell biology international; 29: pp. 101-110.
Alavi, SMH.; Cosson, J. (2006). Sperm motility in fishes. (II) Effects of ions and osmolarity: a review. Cell Biology International; 30: pp. 1-14
Aramli, MS.; Nazari, RM.; Kalbassi, MR.; Aramli, S. (2013). Semen of Beluga, Huso huso: Ionic content and osmolality of seminal plasma and their physiological correlation with sperm motility indices. Fisheries and Aquaculture Journal; 4: 1.
Bagheri, T.; Imanpoor, MR.; Jafari, V.; Bennetau-Pelissero, C. (2013). Reproductive impairment and endocrine disruption ingoldfish by feeding diets containing soybean meal. Animal Reproduction Science; 139: pp. 136-144.
Beenetau-Pelissero, C.; Breton, B.; Bennetau, B.; Corraze, G.; Le Menn, F.; Davail-Cuisset, B.; et al. (2001). Effect of genistein enriched diets on the endocrine process of gametogenesis and on reproduction efficiency of the rainbow trout (Oncorhynchus mykiss). General and Comparative Endocrinology; 121: pp. 173-187.
Bennetau- Pelissero, C.; Bennetau, B.; Babin, P.; Le Menn, F.; Dunogues, J. (1991). The estrogenic activity of certain phytoestrogens in the Siberian sturgeon Acipenser baeri. The Journal of Steroid Biochemistry and Molecular Biology; 38: pp. 292-299.
Billard, R.; Cosson, J.; Perchec, G.; Linhart, O. (1995). Biology of sperm and artificial reproduction in carp. Aquaculture; 129: pp. 95-112.
Bjerselius, R.; Lundstedt-Enkel, K.; Olsen, H.; Mayer, I.; Dimberg, K. (2001). Male goldfish reproductive behavior and physiology are severely affected by exogenous exposure to 17β-estradiol. Aquatic Toxicology; 53: 139-152.
Bjerselius, R.; Olsen, KH.; Zheng, W. (1995). Endocrine, gonadal and behavioral responses of male crucian carp Carassius carassius to the hormonal pheromone 17, 20- dihydroxy-4-pregnen-3-one. Chemical Senses; 20: pp. 221-230.
Bobe, L.; Labbé, C. (2010). Egg and sperm quality in fish. General and Comparative Endocrinology; 165: pp. 535-548.
Chen, S.; Kao, Y.C.; Laughton, C.A. (1997). Binding characteristics of aromatase inhibitors and phytoestrogens to human aromatase. The Journal of Steroid Biochemistry and Molecular Biology; 61: pp. 107-115.
Ciereszko, A.; Glogowski, J.; Dabrowski, K. (2000). Biochemical characteristics of seminal plasma and spermatozoa of fresh water fishes. In: Tiersch, TR.; Mazik, PM.; editors. Cryopreservation in aquatic species. Louisiana: WAS, Baton Rouge; p. 20-48.
Cirezko, A.; Ramseyer, L.; Dabrowski, K.; (1993). Cryopreservation of yellow perch semen. The Progressive Fish-Culturist; 55: pp. 261-264.
Cosson, J.; Groison, AL.; Suquet, M.; Fauvel, C.; Dreanno, C.; Billard, R. (2008). Studying sperm motility in marine fish: an overview on the state of the art. Journal of Applied Ichthyology; 24: pp. 460-486.
Clearwater, SJ.; Crim, LW.; Gonadotropin releasing hormone analogue treatment increased sperm production in yellowtail flounder pleuronectes ferrugineus. Fish Physiology and Biochemistry; 19: pp. 349-357.
Cleveland, BM.; Manor, ML. (2015). Effects of phytoestrogens on growth-related and lipogenic genes in rainbow trout (Oncorhynchus mykiss). Comparative Biochemistry and Physiology; Part C.; 170: pp. 28-37.
Coward, A.; Bromage, NR.; Hibbitt, O.; Parrington, J.; Gametogenesis, fertilization and egg activation in teleost fish. Reviews in fish Biology and fisheries; 12: pp. 33-58.
Dixon, RA.; Ferreira, D.; (2002). Genistein. Phytochemistry; 60: 205-211.
Gabriel, UU.; Akinrotimi, OA.; Ariweriokuma, VS. (2012). Changes in Metabolic Enzymes Activities in Selected Organs and Tissue of Clarias Gariepinus Exposed to Cypermethrin. Journal of Environmental Science and Engineering Technology; 1: 2.
Gallego, V.; Martínez-Pastor, F.; Mazzeo, I.; Peñaranda, DS.; Herráez, MP.; Asturiano, J.F.; Pérez, L. (2014). Intracellular changes in Ca2+, K+ and pH after spermmotility activation in the European eel (Anguilla anguilla): preliminary results. Aquaculture; 418-419: pp. 155-158.
Green, CC.; Kelly, AM. (2008). Effect of the exogenous soyabean phytooestrogen genistein on sperm quality, ATP content and fertilization rates in channel catfish Ictalurus punctatus (Rafinesque) and walleye Sander vitreus (Mitchill). Journal of Fish Biology; 72: pp. 2485-2499.
Huang, R. Q.; Fang, M. J.; Dillon, G. H. (1999). The tyrosine kinase inhibitor genistein directly inhibits GABAA receptors. Molecular Brain Research; 67: pp. 177-183.
Ingerman, R.; Holcomb, M.; Robinson, M. L.; Cloud, J. C. (2002). Carbon dioxide and pH effect sperm motility of white sturgeon (Acipenser transmontanus). Journal of Experimental Biology; 205: pp. 2885-2890.
Itoh, A.; Inaba, K.; Ohtake, H.; Fujinoki, M.; Morisawa, M. (2003). Characterization of Camp-dependent protein kinase catalytic subiunit from rainbow trout spermatozoa. Biochemical and Biophysical Research communication; 305: 855-861.
Judycka, S.; Nynca, J.; Liszewska, E.; Dobosz, S.; Zalewski, T.; Ciereszko, A. (2016). Potassium ions in extender differentially influence the post-thaw sperm motility of salmonid fish. Cryobiology; xxx: pp. 1-9.
Kowalski, R.; Wojtczak, M.; Glogwski, J.; Ciereszko, A. (2003). Gelatinolytic and antitrypsin activities in seminal plasma of common carp: relationship to blood, skin mucus and spermatozoa. Aquatic Living Resources; 16: pp. 438-444.
Krasznai, Z.; Marian, T.; Izumi, H.; Damjanovich, S.; Balkay, L.; Trón, L.; et al. (2000). Membrane hyperpolarization removes inactivation of Ca2 C channels leading to Ca2 C in ux and initiation of sperm motility in the common carp. Proceedings of the National Academy of Sciences of the United States of America; 97: pp. 2052-2067.
Kruger, J.C.; Smit, G.L.; Van Vuren, J.H.J.; Ferreira, J.T. (2006). Some chemical and physical characteristics of the semen of Cyprinus carpio L. and Oreochromis mossambicus (Peters). Journal of Fish Biology; 24: pp. 263-272.
Latonnelle, K.; Le Menn, F.; Bennetau-Pelissero, C. (2000). In vitro estrogenic effects of phytoestrogens in rainbow trout and Siberian sturgeon. Ecotoxicology; 9: pp. 115-125.
Le Bail, JC.; Champavier, Y,; Chulia, AJ.; Habrioux, G. (2000). Effects of phytoestrogens on aromatase, 3β and 17β-hydrosteroid dehydrogenase activities and human breast cancer cells. Life Sciences; 66: pp. 1281-1291.
Lehtinen, KJ.; Mattsson, K.; Tana, J.; Engström, C.; Lerche, Opens overlay Jarl Hemming eO.; Hemming, J. (1999). Effects of wood-related sterols on the reproduction, egg survival, and offspring of brown trout (Salmo trutta lacustris L.). Ecotoxicology and Environmental Safety; 42: pp. 40-49.
Morisawa, M.; Suzuki, K.; Shimizu, H.; Morisawa, S.; Yasuda, K. (1983). Effect of osmolality and potassium on motility of spermatozoa from freshwater cyprinid fishes. Journal of Experimental Biology; 107: pp. 95-103.
Morisawa, M. (2008). Adaptation and strategy for fertilization in the sperm of teleost fish. Journal of Applied Ichthyology ; 24: pp.362-370.
Mylonas, C.C.; Duncan, N.J.; Asturianoc, J.F. (2016). Hormonal manipulations for the enhancement of sperm production in cultured fish and evaluation of sperm quality. Aquaculture; xxx: xxx-xxx.
Nagao, T.; Yoshimura, S.; Saito, Y.; Nakagomi, M.; Usumi, K.; Ono, H. (2001). Reproductive effects in male and female rats of neonatal exposure to genistein. Reproductive Toxicology; 15: pp. 399-411.
Pérez, L.; Vílchez, M.C.; Gallego, V.; Morini, M.; Peñaranda, DS.; Asturiano, J.F. (2016). Role of calciumon the initiation of spermmotility in the European eel. Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology; 191: pp. 98-106.
Piros, B.; Glogowski, J.; Kolman, R.; Rzemieniecki, A.; Domagala, J.; Horváth, Á. (2002). Biochemical characterization of Siberian sturgeon Acipenser beari and starlet, Acipenser ruthenus. Milt plasma and spermatozoa. Fish Physiology and Biochemistry; 26: pp. 289-295.
Rurangwa, E.; Kime, D.E.; Olllevier, F.; Nash, J.P. (2004). The measurement of sperm motility and factors affecting sperm quality in cultured fish. Aquaculture; 234: pp. 1-28.
Secer, S.; Tekin, N.; Bozkurt, Y.; Bukan, N.; Akcay, E. (2004). Correlation between biochemical and spermatological parameters in rainbow trout semen. Israeli Journal of Aquaculture; 56: pp. 274-280.
Shaliutina-Kolešová, A.; Kotas, P.; Štěrba, J.; Rodina, M.; Dzyuba, B.; Cosson, J.; Linhart, O. (2016). Protein profile of seminal plasma and functionality of spermatozoa during the reproductive season in the common carp (Cyprinus carpio) and rainbow trout (Oncorhynchus mykiss). Molecular Reproduction & Development; 83: pp. 968-982.
Shaliutina, A.; Hulak, M.; Dzuyba, B.; Linhart, O. (2012). Spermatozoa motility and variation in the seminal plasma proteome of Eurasian perch (Perca fluviatilis) during the reproductive season. Molecular Reproduction and Development; 79: pp. 879-887.
Soengas, J.L.; Sanmartin, B.; Barrciela, P.; Aldegunde, M.; Rozas, G. (1993). Changes in carbohydrate metabolism in domesticated rainbow trout Onchorhynchus mykiss related spermatogenesis. Comparative Biochemistry and Physiology Part B: Comparative Biochemistry; 105: pp. 665-67.
Verma, DK.; Routray, P.; Dash, C.; Dasgupta, S.; Jena, J.K. (2009). Physical and Biochemical Characteristics of Semen and Ultrastructure of Spermatozoa in Six Carp Species. Turkish Journal of Fisheries and Aquatic Sciences; 9: pp. 67-76.
Zadmajid, V. (2016). Comparative effects of human chorionic gonadotropin (hCG) and Ovaprim™ (sGnRHa + domperidone) on the reproductive characteristics of wild-caught male Longspine scraper, Capoeta trutta (Heckel, 1843). Aquaculture; 463: pp. 7-15.
Zadmajid, V.; Imanpoor, M.R. (2009). The correlation between some biochemical and spermatological parameters in goldfish (Carassius auratus) semen. Journal of Agricultural Sciences and Natural Resources; Vol. 16 (1).
Zadmajid, V.; Imanpoor, M.R.; Soudagar, M.; Shabani, A. (2008). The effects of GnRHa, HCG and Pituitary extract on biochemical parameters of seminal plasma in goldfish (Carassius auratus gibelio). Iranian Journal of Biology; 2(22): pp. 333-342
Zadmajid, V.; Imanpoor, MR.; Sudagar, M.; shabany, A. (2008). The effects of ovafact (GnRHa) on biological characteristics of semen in commons, comets, wakins and fantails goldfish (Carassius auratus gibelio). Veterinary Journal (Pajouhesh & Sazandegi); 83: pp. 9-17.
Zhang, L.; Ikhlas, A.; Foran, C.M. (2002). Characterization of the estrogenic response to genistein in Japanese medaka (Oryzias latipes). Comparative Biochemistry and Physiology; 132: pp. 203-211.
Zheng, W.; strobeck, C.; Stacey, N.E. (1997). The steroid pheromone 17α, 20β, dihydroxy -4-prognen-3-one increases fertility and paternity in gold fish. Journal of Experimental Biology; 200: pp. 2833-2840.
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