Affiliation:
1. College of Veterinary Science Assam Agricultural University Guwahati Assam India
2. ICAR‐National Research Centre on Pig Guwahati Assam India
3. Krishi Vigyan Kendra Assam Agricultural University Karimganj Assam India
Abstract
AbstractIn vitro capacitation allows for a greater understanding of the mechanisms underlying fertilization and the development of improved reproductive techniques for improving fertility rates in porcine. Tyrodes albumin lactate pyruvate (TALP) and modified Krebs Ringers Broth (m‐KRB) are two medias that are commonly used in research experiments to induce capacitation in boar spermatozoa (Cañón‐Beltrán et al., Theriogenology, 198, 2023 and 231; Oberlender et al., Archivos de Medicina Veterinaria, 44, 2012 and 201; Sahoo et al., International Journal of Biological Macromolecules, 241, 2023 and 124502). Moreover, understanding the morphological and functional changes in boar spermatozoa at different hours of capacitation periods might aid in the development of novel techniques for improving sperm quality and increasing the litter size. This study was carried out to investigate the effect of Tyrode albumin lactate pyruvate and modified Krebs Ringers Broth media on in vitro capacitation of HD‐K75 boar spermatozoa at three different periods of incubation. A total of 24 ejaculate from four clinically healthy, 10–12 months aged HD‐K75 boars, maintained at ICAR‐All India Coordinated Research Project (AICRP) on pig were selected. Semen was collected by ‘Simple fist’ method using a portable dummy. The semen samples having 200 mL volume, 103 × 106 spermatozoa/ml concentration and 70% initial motility were selected and split into two parts and suspended in TALP and m‐KRB media, respectively, and incubated for 5 h at 37°C. Seminal parameters viz. sperm viability, plasma membrane integrity and acrosomal integrity were estimated in the samples at 0, 3 and 5 h of incubation. This study revealed that there was significant variation between media in live acrosome‐reacted (p < .05) and HOST‐reacted (p < .01) spermatozoa, while between capacitation periods significant (p < .01) variation was observed in hyperactivated spermatozoa, live acrosome‐reacted spermatozoa, HOST‐reacted spermatozoa, FITC‐labelled PSA, extracellular protein and sperm cholesterol. Non‐significant variation was observed in total phospholipid. TALP showed overall better consequence on sperm viability, plasma membrane and acrosomal integrity of boar spermatozoa. From this study, it could be concluded that both TALP and m‐KRB media were virtuous to induce capacitation in HD‐K75 boar spermatozoa. TALP media, however, had a better effect on sperm viability, plasma membrane and acrosomal integrity of boar spermatozoa. Out of the three different periods, 3 h capacitation period resulted in significantly (p < .01) higher incidence of sperm viability, plasma membrane and acrosomal integrity in HD‐K75 boar spermatozoa.