ROLE OF KISSPEPTIN AS A SUBSTITUTE OF GnRH IN OVSYNCH PROTOCOL IN EWES

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Date
2019-02-18
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pvnrtvu
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The aim of the present study “The role of kisspeptin as a substitute of GnRH in Ovsynch protocol in ewes” was conducted on 18 healthy and non-pregnant ewes to study the fertility parameters upto conception and FSH and LH levels in serum during synchronisation protocol. The selected 18 ewes were randomly divided into 3 groups containing 6 each. In GnRH group all the ewes were administered with 1ml of Receptal@ VET ( each ml contains 0.0042mg Buserelin acetate 0.0042 mg equivalent to 0.004 mg buserelin) intramuscularly on 0 and 9th day. On 7th day of the protocol Vetmate about 125 μg (Each ml contains Cloprostenol (Synthetic Prostaglandin F2α) 250 μg / ml) was administered intramuscularly to all the ewes. In kisspeptin group all the ewes were administered with 10μg of kisspeptin per kg body weight intravenously on 0 and 9th day. On 7th day of the protocol Vetmate about 125 μg (Each ml contains Cloprostenol (Synthetic Prostaglandin F2α) 250 μg / ml) was administered intramuscularly to all the ewes. In control group all the ewes were administered with about 5ml of normal saline intravenously on 0, 7, 9th day. About 4ml of blood was collected from all the ewes in GnRH, kisspeptin and control groups on 0 and 9th day 30 minutes before and 30 minutes after injection of receptal, kisspeptin and normal saline in GnRH, kisspeptin and control groups respectively. The estrous response rate was 100%, 66.67% and 16.67% respectively in GnRH, kisspeptin and control groups. The statistical analysis showed a significant difference (p≤0.05) in between the groups. The estrous response rate was higher in treatment groups compared to control groups. The estrous length (hours) in GnRH, kisspeptin and control groups was 18.00 ± 2.19, 11.66 ± 4.11 and 2.00 ± 2.00 respectively. The estrous length statistically differed (p≤0.05) in treatment groups compared to control groups. Conception rate was 83.33%, 50% and 16.67% in GnRH, kisspeptin and control groups respectively. A significant difference was observed in between the groups. The conception rate was better in GnRH group and kisspeptin group than control group. The follicle stimulating hormone (FSH) levels in serum in GnRH group on 0 day before injection of receptal was 0.39 ± 0.04 ng/ml and after injection was 1.56 ± 0.18 ng/ml. On 9th day the FSH levels in GnRH group before injection of receptal was 0.5 ± 0.05 ng/ml and after injection was 2.41 ± 0.31 ng/ml. The FSH levels in kisspeptin group before injection of kisspeptin on 0 day was 0.3 ± 0.06 ng/ml. FSH levels in serum after injection of kisspeptin on 0 day was 0.93 ± 0.29 ng/ml. The FSH levels on 9th day before injection of kisspeptin was 0.38 ± 0.05 ng/ml. FSH levels in serum after injection of kisspeptin on 9th day was 1.39 ± 0.37 ng/ml. In control group the FSH levels remained almost same on 0 and 9th day of the protocol. The mean FSH levels were significantly higher in GnRH group compared to other groups. There was a significant difference (p≤0.05) in the FSH levels in serum between the groups. The leutinising hormone (LH) levels in serum in GnRH group on 0 day before injection of receptal was 0.18 ± 0.02 ng/ml. LH levels after injection of receptal was 0.72 ± 0.06 ng/ml. On 9th day the LH levels in serum before injection of receptal was 0.3 ± 0.04 ng/ml and after injection the levels of LH was 0.68 ± 0.06 ng/ml. The LH levels in kisspeptin group on 0 day before injection of kisspeptin was 0.23 ± 0.03 ng/ml and after injection of kisspeptin was 1.37 ± 0.39 ng/ml. On 9th day the LH levels before injection of kisspeptin was 0.40 ± 0.04 ng/ml and after injection the levels of LH was 1.86 ± 0.33 ng/ml. In control group the levels of LH were almost similar on all days. Comparatively there existed a significant difference (p≤0.05) in the mean LH levels in between the groups. In conclusion the treatment with Kisspeptin was better when compared with control group but less response was observed when compared with GnRH group
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