1-Title: Sperm phenotype and flowcytometry parameters in productive buffalo bulls of different age

1-Title: Sperm phenotype and flowcytometry parameters in productive buffalo bulls of different age
Authors: KV Jayanthi, GS Naveen Kumar, M Ashokan, K Hemanth Gowda, D Ramesh, Shivan Gouda Patil and A Kumaresan
Source: Ruminant Science (2023)-12(2):185-190.

Abstract

How to cite this manuscript: Jayanthi KV, Kumar GS Naveen, Ashokan M, Gowda K Hemanth, Ramesh D, Patil Shivan Gouda and Kumaresan A (2023). Sperm phenotype and flowcytometry parameters in productive buffalo bulls of different age. Ruminant Science 12(2):185-190.
Abstract
The present study aimed to analyze sperm phenotypic and flow cytometry parameters and their association with age among healthy breeding Murrah buffalo bulls. Data on sperm phenotypic characters of twenty Murrah buffalo bulls of different ages and in semen production stationed at Nandini Sperm Station, Bengaluru were analyzed immediately after semen collection, and semen straws of the same bulls were subjected to semen flow cytometry analysis. Buffalo bulls were divided into three groups based on age G-I (33-36 months), G-II (49-63months), and G-III (72-113 months). The mean±SE of semen phenotypic characters ejaculate volume, semen pH, sperm concentration, initial motility, and post-thaw motility were 3.867±0.059 ml, 6.479±0.017, 1347±65.84 (106/ml), 77.778±1.22 (%) and 41.627±1.65 (%), respectively. A significantly higher ejaculate volume, pH, post-thaw motility and lower sperm concentration with age was observed. The mean flow cytometry parameter values were sperm acrosomal integrity (LAI% (44.93±2.94), LAR% (8.49±0.51), DAI% (7.81±0.62) and DAR % (38.11±2.61)), plasma membrane integrity (total live % 48.20±3.10 and dead % 42.83±4.65), mitochondrial reactive oxygen species (62.69±2.66 %) and intracellular calcium concentration (LLC % (16.30±1.37), LHC % (38.27±2.52), DLC % (34.39±2.68) and DHC % (11.03±0.87)). However, flow cytometric parameters were not significantly associated with age among productive healthy bulls.
References
Ahmed S, Khan MIUR, Ahmad M and Iqbal S (2018). Effect of age on lipid peroxidation of fresh and frozen-thawed semen of Nili-Ravi buffalo bulls. Italian Journal of Animal Sciences 17(3):730-735.
Aitken RJ and Curry BJ (2011). Redox regulation of human sperm function: from the physiological control of sperm capacitation to the etiology of infertility and DNA damage in the germ line. Antioxidant Redox Signal 14(3):367-381.
Aitken RJ, Irvine DS and Wu FC (1991). Prospective analysis of sperm-oocyte fusion and reactive oxygen species generation as criteria for the diagnosis of infertility. American Journal of Obstetrics and Gynecology 164(2):542-551.
Anand Mukul, Yadav Sarvajeet, Yadav Brijesh, Dhariya Rahul and Chaudhary Deependra (2023). Protective effect of quail egg yolk on sperm characteristics of Barbari buck semen during short-term storage at 4 ºC. Ruminant Science 12(1):95-98.
Aurich C (2005). Factors affecting the plasma membrane function of cooled-stored stallion spermatozoa. Animal Reproduction Science 89(1-4):65-75.
Chang J, Yang JY, Choi J, Jung HH and Im GJ (2011). Calcium imaging in gentamicin ototoxicity: increased intracellular calcium relates to oxidative stress and late apoptosis. International Journal of Pediatric Otorhinolaryngology 75(12):1616-1622.
De Lamirande E and Cagnon C (1993). Human sperm hyperactivation and capacitation as parts of an oxidative process. Free Radical Biology Medicine 14(2):157-166.
De Lamirande E, Jiang H, Zini A, Kodama H and Gagnon C (1997). Reactive oxygen species and sperm physiology. Revolutionary Reproduction 2:48-54.
Gliozzi TM, Turri F, Manes S, Cassinelli C and Pizzi F (2017). The combination of kinetic and flow cytometric semen parameters as a tool to predict fertility in cryopreserved bull semen. Animal 11(11):1975-1982
Gosalvez J, Tvrda E and Agarwal A (2017). Free radical and superoxide reactivity detection in semen quality assessment: past, present and future. Journal of Assisted Reproduction and Genetics 34(6):697-707
Javed MT, Khan A and Kausar R (2000). Effect of age and season on some semen parameters of Nili-Ravi buffalo (Bubalus bubalis) bulls. Veterinary Arh 70(2):83-94.
Kanno C, Kang SS, Kitade Y, Yanagawa Y, Takahashi Y and Nagano M (2016). Simultaneous evaluation of plasma membrane integrity, acrosomal integrity, and mitochondrial membrane potential in bovine spermatozoa by flow cytometry. Zygote 24(4):529-536.
Koonjaenak S, Johannisson A, Pongpeng P, Wirojwuthikul S, Kunavongkrit A and Rodriguez-Martinez H (2007). Seasonal variation in nuclear DNA integrity of frozen–thawed spermatozoa from Thai AI swamp buffaloes (Bubalus bubalis). Journal of Veterinary Medicine Series A 54(7):377-383.
Kumar A, Singh G, Jerome A, Kumar P, Arjun V, Bala R, Verma N and Sharma RK (2021). IGF-1 supplementation in semen affects mitochondrial functional and calcium status of buffalo sperm following cryopreservation. Animal Reproduction Sciences 231:106783
Kumar Mahesh, Kumar Anuj, Sachan Vikas, Agarwal JK, Saxena Atul, Singh Avaneesh Kumar, Gupta Shashi Kant and Swain Dilip (2022). Effect of resveratrol supplementation on the semen quality of cryopreserved Hariana bull semen. Ruminant Science 11(2):475-478.
Kumar Chandan, Kumar Ankesh, Kumar Anil, Archana, Shekhar Pallav and Kumar Ajeet (2023). Study on effect of tert-butyl hydroquinone on Red Sindhi bull semen cryopreservation. Ruminant Science 12(1):143-148.
Kumaresan A, Johannisson A, Al-Essawe EM and Morrell JM (2017). Sperm viability, reactive oxygen species, and DNA fragmentation index combined can discriminate between above-and below-average fertility bulls. Journal of Dairy Sciences 100(7):5824-5836
Malama E, Zeron Y, Janett F, Siuda M, Roth Z and Bollwein H (2017). Use of computer-assisted sperm analysis and flow cytometry to detect seasonal variations of bovine semen quality. Theriogenology 87:79-90.
Minervini F, Guastamacchia R, Pizzi F, Dell’aquila ME and Barile VL (2013). Assessment of different functional parameters of frozen-thawed buffalo spermatozoa by using cytofluorimetric determinations. Reproduction in Domestic Animals 48(2):317-324.
Mustapha AR, Beigh YA, Abhishek K, Rahul K, Omer D, Kumar A, Prasad JK, Bhure S, Srivastava N and Ghosh SK (2017). Effects of partial deoxygenation of extender on plasma membrane integrity and enzyme activity in frozen-thawed crossbred bull semen. Ruminant Science 6(2):327-331.
Patil S, Kumar P, Singh G, Bala R, Jerome A, Patil CS, Kumar D, Singh S and Sharma RK (2020). Semen dilution effect on sperm variables and conception rate in buffalo. Animal Reproduction Sciences 214:106304.
Shah Nadeem, Yadav HP, Gupta RK, Chauhan DS, Singh Vijay, Yadav Sarvajeet and Swain DK (2016). Comparative evaluation of acrosomal integrity of bull spermatozoa by two staining techniques. Ruminant Science 5(2):253-256.
Singh Vipin, Kumar Anuj, Yadava CL, Patel Akhil, Yadav Brijesh, Panday Vijay and Saxena Atul (2018). Effect of season on certain seminal plasma enzymes profile at pre-freeze and post thaw period in the Haryana bull. Ruminant Science 7(2):279-282.
Thomas CA, Garner DL, Mel Dejarnette J and Marshall CE (1997). Fluorometric assessments of acrosomal integrity and viability in cryopreserved bovine spermatozoa. Biology Reproduction 56(4):991-998.
Younis M, Samad HA, Ahmad N and Ahmad I (1998). Studies on semen quality of young, adult and old buffalo bulls during low and peak breeding seasons. Pakistan Veterinary Journal 18:134-141.