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The effect of different concentrations of taxifolin on the quality of frozen and thawed semen of Simmental cattle | ||
| Iranian Journal of Veterinary Research | ||
| دوره 24، شماره 3 - شماره پیاپی 84، 2023، صفحه 235-241 اصل مقاله (283.78 K) | ||
| نوع مقاله: Full paper (Original article) | ||
| شناسه دیجیتال (DOI): 10.22099/ijvr.2023.47455.6849 | ||
| نویسندگان | ||
| S. Zolfaghari1؛ E. Ayen* 2؛ A. Khaki3 | ||
| 1Ph.D. Student in Theriogenology, Department of Theriogenology and Poultry Disease, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran | ||
| 2Department of Theriogenology and Poultry Disease, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran | ||
| 3Department of Clinical Sciences, Faculty of Veterinary Medicine, Amol University of Special Modern Technologies, Amol, Iran | ||
| چکیده | ||
| Background: Artificial insemination (AI) is one of the most important reproductive technologies used to modify animals genetically. Using this method, the genetic composition of the herd can be improved and selected by choosing bulls with excellent genetic characteristics. Taxifolin (TXF), a plant flavonoid, has shown an antioxidative effect. Aims: The current study aimed to evaluate the impact of TXF on the quality of frozen-thawed semen in Fleckvieh (Simmental) dual-purpose bulls. Methods: Freezable semen specimens were obtained by an artificial vagina. Ejaculates were equally divided into six parts for six experimental groups, including without adding TXF to diluent (C), adding 25 (T25), 50 (T50), 100 (T100), 200 (T200), and 400 (T400) μM TXF. Sperms were frozen in a one-step dilution method. Semen factors, including motility, viability, sperm membrane integrity, DNA damage, and oxidant and antioxidant enzyme activities, were examined after thawing. Results: Our findings revealed that all semen quality parameters, antioxidant enzyme activities, and free radical levels were superior in TXF-treated groups compared to the control group, and the differences were noticeably higher in the T100 group than the other groups. Conclusion: Adding 100 μM TXF to diluent could improve the quality of bull frozen semen. | ||
| کلیدواژهها | ||
| Semen quality؛ Simmental؛ Taxifolin | ||
| مراجع | ||
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Abeydeera, LR; Wang, WH; Cantley, TC; Prather, RS and Day, BN (1998). Presence of beta-mercaptoethanol can increase the glutathione content of pig oocytes matured in vitro and the rate of blastocyst development after in vitro fertilization. Theriogenology. 50: 747-756.
Agarwal, A; Nallella, KP; Allamaneni, SS and Said, TM (2014). Role of antioxidants in treatment of male infertility: an overview of the literature. Reprod. Biomed., 8: 616-627.
Agarwal, A; Saleh, RA and Bedaiwy, MA (2003). Role of reactive oxygen species in the pathophysiology of human reproduction. Fertil. Steril., 79: 829-843.
Ahmadi, S; Bashiri, R; Ghadiri-Anari, A and Nadjarzadeh, A (2016). Antioxidant supplements and semen parameters: An evidence-based review. Int. J. Reprod. Biomed., 14: 729-736.
Aitken, R; Buckingham, D and Harkiss, D (1993). Use of a xanthine oxidase free radical generating system to investigate the cytotoxic effects of reactive oxygen species on human spermatozoa. Reproduction. 97: 441-450.
Alvarez, JG and Storey, BT (1992). Evidence for increased lipid peroxidative damage and loss of superoxide dismutase activity as a mode of sublethal cryodamage to human sperm during cryopreservation. J. Androl., 13: 232-241.
Bailey, JL; Bilodeau, JF and Cormier, N (2000). Semen cryopreservation in domestic animals: a damaging and capaciting phenomenon. J. Androl., 21: 1-7.
Bartoň, L; Kudrna, V; Bureš, D; Zahrádková, R and Teslík, V (2007). Performance and carcass quality of Czech Fleckvieh, Charolais and Charolais × Czech Fleckvieh bulls fed diets based on different types of silages. Czech J. Anim. Sci., 52: 269-276.
Baumber, J; Ball, BA; Linfor, JJ and Meyers, SA (2003). Reactive oxygen species and cryopreservation promote DNA fragmentation in equine spermatozoa. J. Androl., 24: 621-628.
Bilodeau, JF; Chatterjee, S; Sirard, MA and Gagnon, C (2000). Levels of antioxidant defenses are decreased in bovine spermatozoa after a cycle of freezing and thawing. Mol. Reprod. Dev., 55: 282-288.
Brito, LF; Silva, AE; Barbosa, RT and Kastelic, JP (2004). Testicular thermoregulation in Bos indicus, crossbred and Bos taurus bulls: relationship with scrotal, testicular vascular cone and testicular morphology, and effects on semen quality and sperm production. Theriogenology. 61: 511-528.
Buffone, MG; Calamera, JC; Brugo-Olmedo, S; De Vincentiis, S; Calamera, MM; Storey, BT; Doncel, GF and Alvarez, JG (2012). Superoxide dismutase content in sperm correlates with motility recovery after thawing of cryopreserved humanspermatozoa. Fertil. Steril., 97: 293-298.
Castro, LS; Hamilton, TRS; Mendes, CM; Nichi, M; Barnabe, VH and Azumpcao, MEOA (2016). Sperm cryodamage occurs after rapid freezing phase: flow cytometry approach and antioxidant enzymes activity at different stages of cryopreservation. J. Anim. Sci. Biotechnol., 7: 17-25.
Catalá, A (2013). Five decades with polyunsaturated fatty acids: chemical synthesis, enzymatic formation, lipid peroxidation and its biological effects. J. Lipids. : 1-19.
Cojkic, A and Morrell, JM (2023). Animal welfare assessment protocols for bulls in artificial insemination centers: requirements, principles, and criteria. Animals., 13: 942.
Filipčík, R; Falta, D; Kopec, T; Chládek, G; Večeřa, M and Rečková, Z (2020). Environmental factors and genetic parameters of beef traits in Fleckvieh cattle using field and station testing. Animals. 10: 2159. doi: 10.3390/ ani10112159.
Gadea, J; Gumbao, D; Cánovas, S; García-Vázquez, FA; Grullón, LA and Gardón, JC (2008). Supplementation of the dilution medium after thawing with reduced glutathione improves function and the in vitro fertilizing ability of frozen-thawed bull spermatozoa. Int. J. Androl., 31: 40-49.
Galeati, G; Vallorani, C; Bucci, D; Bernardini, C; Tamanini, C; Parmeggiani, A and Spinaci, M (2010). Daidzein does affect progesterone secretion by pig cumulus cells but it does not impair oocytes IVM. Theriogenology. 74: 451-457.
Garner, DL and Hafez, ESE (2013). Spermatozoa and seminal plasma. In: Hafez, B and Hafez, ESE (Eds.), Reproduction in farm animals. (7th Edn.), Philadelphia, Wiley-Blackwell. PP: 96-110.
Gil, J; Lundehei, N; Soderquist, L and Rodriiuuez-Marinez, H (2003). Influence of extender, temperature and addition of glycerol on post-thaw sperm parameters in ram semen. Theriogenology. 59: 1241-1255. Götz, KU; Luntz, B; Robeis, J; Edel, C; Emmerling, R; Buitkamp, J; Anzenberger, H and Duda, J (2015). Polled Fleckvieh (Simmental) cattle - current state of the breeding program. Livest. Sci., 179: 80-85.
Gredler, B; Nirea, KG; Solberg, TR; Egger-Danner, C; Meuwissen, THE and Sölkner, J (2009). Genomic selection in Fleckvieh/Simmental-First results. Interbull Bulletin. 40: 209-213.
Itri, R; Junqueira, HC; Mertins, O and Baptista, MS (2014). Membrane changes under oxidative stress: the impact of oxidized lipids. Biophys. Rev., 6: 47-61.
Katayose, H; Yanagida, K; Hashimoto, S; Yamada, H and Sato, A (2003). Use of diamide-acridine orange fluorescence staining to detect aberrant protamination of human-ejaculated sperm nuclei. Fertil. Steril., 79: 670-676.
Makker, K; Agarwal, A and Sharma, R (2009). Oxidative stress and male infertility. Indian J. Med. Res., 129: 357-367.
Nebel, RL (2007). Techniques for artificial insemination of cattle with frozen thawed semen. In: Current therapy in large animal theriogenology. (2nd Edn.), Missouri, Elselvier PP: 253-258.
Perišić, P; Skalicki, Z; Petrović, MM; Bogdanović, V and Ružić-Muslić, D (2009). Simmental cattle breed in different production systems. Biotechnol. Anim. Husb., 25: 315-326.
Petruska, P; Capcarova, M and Sutovsky, P (2014). Antioxidant supplementation and purification of semen for improved AI in livestock species. Turkish J. Vet. Anim. Sci., 38: 643-652.
Rao, M; Zhao, XL; Yang, J; Hu, SF; Lei, H; Xia, W and Zhu, CH (2015). Effect of transient scrotal hyperthermia on sperm parameters, seminal plasma biochemical markers, and oxidative stress in men. Asian J. Androl., 17: 668-675.
Sanocka, D and Kurpisz, M (2004). Reactive oxygen species and sperm cells. Reprod. Biol. Endocrinol., 2: 1-7.
Sikka, SC (1996). Oxidative stress and role of antioxidants in normal and abnormal sperm function. Front. Biosci., 1: 78-86.
Tahmasbian, H; Ayen, E and Khaki, A (2022). Evaluation of the effects of hesperidin on fresh and frozen-thawed semen quality using two different cryopreservation methods in Simmental bull. Anim. Reprod., 19: e20220042. doi: 10.1590/1984-3143-AR2022-0042.
Thompson, A; Agarwal, A and Du Plessis, SS (2014). Physiological role of reactive oxygen species in sperm function: a review. In: Parekattil, SJ and Agarwal, A (Eds.), Antioxidants in male infertility: a guide for clinicians and researchers. New York, Springer Science and Business Media. PP: 69-89.
Tvrdá, E; Kňažická, Z; Bárdos, L; Massányi, P and Lukáč, N (2011). Impact of oxidative stress on male fertility—A review. Acta Vet. Hung., 59: 465-484.
Ugur, MR; Saber Abdelrahman, A; Evans, HC; Gilmore, AA; Hitit, M; Arifiantini, RL; Purwantara, B; Kaya, A and Memili, E (2019). Advances in cryopreservation of bull sperm. Front. Vet. Sci., 6: 268. doi: 10.3389/fvets.2019.00268. | ||
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