| Literature DB >> 34146972 |
Pradeep Nag1, Arumugam Kumaresan2, Sivamanikandan Akshaya1, Ayyasamy Manimaran3, Duraisamy Rajendran4, Nilendu Paul1, Ankur Sharma1, Thirumalaisamy Karuthadurai1, Saraf Kaustubh1, Sakthivel Jeyakumar3, Kerekoppa Ramesha3.
Abstract
In the present study, we standardized an in vitro oviduct explants model for cattle and assessed the oviduct explants binding ability and phenotypic characteristics of spermatozoa obtained from breeding bulls with high- and low-sperm DNA fragmentation index (DFI%). Cryopreserved spermatozoa from Holstein Friesian crossbred breeding bulls (n = 45) with known field fertility were assessed for DFI% and were classified into either high DFI% or low DFI% category. Flow cytometry was used to assess sperm membrane integrity, acrosome reaction status, mitochondrial membrane potential and intracellular calcium concentrations. It was found that spermatozoa from bulls with low DFI% had significantly higher (P < 0.05) membrane integrity, acrosome intactness, and mitochondrial membrane potential. To assess the sperm oviduct binding ability, oviduct explants were prepared by incubating the oviduct cells overnight in TCM-199 medium at 38.5 °C under 5% CO2. Different sperm concentrations and times of incubation were evaluated and found that 2 million spermatozoa and 1-h incubation yielded high binding index (BI). The BI was also significantly (P < 0.01) higher (>2 times) in the bulls with low-DFI% as compared to high DFI% bulls. The correlation between binding index and DFI% was negative and significant (r = -0.528; P < 0.05). Further, the binding index was positively correlated with conception rate (r = 0.703), intact sperm membrane (r = 0.631) and mitochondrial membrane potential (r = 0.609). It is inferred that sperm phenotypic characteristics and oviduct binding ability are impaired in breeding bulls with high sperm DFI%, which might be associated with low conception rates in these bulls.Entities:
Keywords: Binding index; Bull; Field fertility; Oviduct explant model; Sperm DNA fragmentation
Year: 2021 PMID: 34146972 DOI: 10.1016/j.theriogenology.2021.06.006
Source DB: PubMed Journal: Theriogenology ISSN: 0093-691X Impact factor: 2.740