EVALUATION OF SEMEN QUALITY ON LIQUID STORAGE OF SPECIFIC FRACTIONS OF LARGE WHITE YORKSHIRE BOAR SEMEN

dc.contributor.advisorHarshan, Hiron M.
dc.contributor.authorMALATI NAIK
dc.date.accessioned2021-01-12T05:08:30Z
dc.date.available2021-01-12T05:08:30Z
dc.date.issued2019-08-09
dc.description.abstractThe present research was carried out to assess the quality of Large White Yorkshire (LWY) boar semen in specific fractions within an ejaculate and to assess the keeping quality of fractions of LWY boar semen stored in liquid state at 15C. Two fractions of the semen were taken for the study, initial 10 mL of sperm rich fraction (SRF) formed F1/Group I, rest of the sperm rich fraction formed F2/group II and mixture of half of F1 and F2 each formed group III. A total of 30 ejaculates were used for the study as fractions from four adult healthy LWY boars (16 in Phase I and 14 in Phase II). In phase I, differences in fresh semen characteristics of F1 and F2 were evaluated with respect to pH, concentration, seminal plasma protein content and SDS PAGE profile were analysed. Significant differences were observed between fractions with respect to pH and sperm concentration. The sperm progressive motility and total protein content of semen did not differ significantly between F1 and F2 fraction. An average number of 13.5 ± 0.51 bands were observed in F1, 12.92 ± 0.44 bands in F2 and 12.78 ± 0.23 bands in the sperm free fraction. The proteins observed varied in the molecular weight from 18 - 244 kDa, 8 – 242 kDa and 9 – 248 kDa in F1, F2 and sperm free fraction, respectively. In Phase II of study, semen fractions were analyzed for their keeping quality at 15C after being extended in BTS as group I, group II and group III. Semen was extended with BTS to a final concentration of 50 × 106 sperms/mL and gradually cooled to 22°C, held at same temperature for three hours. The semen was subsequently cooled to 15°C and stored for 72h and evaluated at 4, 24, 48 and 72 h of storage. The pH of semen was significantly (p < 0.01) higher in group II at all time point intervals. The progressive motility of semen was significantly (p < 0.05) higher in group I at 24h, 48 h and 72 h of storage. The sperm viability was significantly higher (p < 0.05) in group I at 72 h of storage alone. The sperm abnormality, acrosome integrity and rapid HOS response was significantly higher in group I at 24 h, 48 h and 72 h of storage alone. Sperm plasma membrane integrity showed a trend of being higher in group I at 72 h of liquid storage (p < 0.1). The cholesterol values at 0h and 72h was significantly higher (p < 0.01) in group I than other groups. The study revealed that initial 10 mL of SRF had showed better preservability at 15C than rest of SRF.en_US
dc.identifier.urihttps://krishikosh.egranth.ac.in/handle/1/5810159830
dc.keywordsLARGE WHITE YORKSHIRE BOAR SEMEN, Nutrients, Regulating pH (Buffers), Osmotic pressure, Antibiotics , Chelating agents , Beltsville Thawing Solution ,en_US
dc.language.isoEnglishen_US
dc.pages98en_US
dc.publisherCOLLEGE OF VETERINARY AND ANIMAL SCIENCES, POOKODE WAYANADen_US
dc.research.problemSEMEN QUALITY ON LIQUID STORAGE OF SPECIFIC FRACTIONS OF LARGE WHITE YORKSHIRE BOAR SEMENen_US
dc.subAnimal Reproduction, Gynaecology and Obstetricsen_US
dc.themeEVALUATION OF SEMEN QUALITY ON LIQUID STORAGE OF SPECIFIC FRACTIONS OF LARGE WHITE YORKSHIRE BOAR SEMENen_US
dc.these.typeM.V.Sc.en_US
dc.titleEVALUATION OF SEMEN QUALITY ON LIQUID STORAGE OF SPECIFIC FRACTIONS OF LARGE WHITE YORKSHIRE BOAR SEMENen_US
dc.typeThesisen_US
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