Superovulatory responsiveness and embryonic development in Iranian Afshari ewes treated with two different concentrations of bovine somatotropin


Abstract views: 222 / PDF downloads: 53

Authors

  • AMIR HOSSEIN ASGARI SAFDAR Islamic Azad University, Baft, Iran

https://doi.org/10.56093/ijans.v86i6.59190

Keywords:

Afshari ewes, Bovine somatotropin, Embryo transfer, IGF-1, Insulin

Abstract

Bovine somatotropin (bST) was administered @ 50 and 100 mg at the beginning of the estrus synchronization and natural mating of the sheep to evaluate the improvement of the ovulation rate, embryonic development and pregnancy rate of the transferred embryos. Donors (48) were treated with 3 different types of treatment; group A (15): treated with bST-100, received 100 mg of bST at the beginning of the synchronization and natural mating, group B (15): treated with 50 mg of bST same as the previous group and control (18) did not receive any type of bST. Each recipient (108) received 2 embryos: 30 recipients received embryos from bST-100s, 45 received the embryos from bST-50 and 33 received embryos from the control group. Using SAS related GENMOD method, superovulatory response, embryo recovery, cleavage rate, transferable embryo percentage, quality of embryos, rates of pregnancy and embryonic development were analyzed. Using GLM procedure, numbers of corpus luteum and blastocyst cells were analyzed. The results showed that bST administration had no significant effect on superovulatory response, number of CL and recovered structures. Number of transferable embryos and embryos that had reached to the blastocyst in bST-50 was more than bST-100 and control group. In conclusion, treatment 50 mg bovine somatotropins enhance the ratio and growth of the transferable embryos. Embryos of bST-50 treatment indicated an improved embryonic development but bST did not affect the pregnancy rates of transferred embryos.

Downloads

Download data is not yet available.

References

Adamiak S J, Mackie K, Watt R G, Webb R and Sinclair K D. 2005. Impact of nutrition on oocyte quality: cumulative effects of body composition and diet leading to hyperinsulinemiain cattle. Biology of Reproduction 73: 918–26. DOI: https://doi.org/10.1095/biolreprod.105.041483

Augustin R, Pocar P, Wrenzycki C, Niemann H and Fischer B. 2003. Mitogenic and anti-apoptotic activity of insulin on bovine embryos produced in-vitro. Reproduction 126: 91–99. DOI: https://doi.org/10.1530/rep.0.1260091

Bari F, Khalid M, Haresign W, Murray A and Merrell B. 2000. Effect of mating system, ûushing procedure, progesterone dose and donor ewe age on the yield and quality of embryos within a MOET program in sheep. Theriogenology 53: 727–42. DOI: https://doi.org/10.1016/S0093-691X(99)00270-8

Betancourt-Alonso M A, Flores-Pérez F I, Rosas-Velasco C and Pérez-Martínez M. 2006. Role of cytokines in embryo implantation in domestic mammals. Veterinaria México 37: 335–50.

Bilby T R, Guzeloglu A, Kamimura S, Pancarci S M, Michel F, Head H H and Thatcher W W. 2004. Pregnancy and bovine somatotropin in nonlactating dairy cows. 1. Ovarian, conceptus, and insulin-like growth factor system responses. Journal of Animal Science 87: 3256–67. DOI: https://doi.org/10.3168/jds.S0022-0302(04)73462-1

Bilby T R, Sozzi A, Lopez M M, Silvestre F T, Ealy A D, Staples C R and Thatcher W W. 2006. Pregnancy, bovine somatotropin, and dietary n-3 fatty acids in lactating dairy cows. 1. Ovarian, conceptus, and growthhormone-insulin-like growth factor system responses. Journal of Dairy Science 89: 3360–74. DOI: https://doi.org/10.3168/jds.S0022-0302(06)72373-6

Block J, Wrenzycki C, Niemann H, Herrmann D and Hansen P J. 2008. Effects of insulin-like growth factor-1 on cellular and molecular characteristics of bovine blastocysts produced in vitro. Molecular Reproduction and Development 75: 895–903. DOI: https://doi.org/10.1002/mrd.20826

Camacho L E, Benavidez J M and Hallford D M. 2008. Pregnancy rates and serum insulin-like growth factor-1, triiodothyronine, and progesterone proûles in rambouilletewes treated with recombinant bovinesomatotropin before breeding. Proceedings, Western Section. American Society of Animal Science 59: 249–52.

Carrillo F, Hernández-Cerón J, Orozco V, Hernández J A and Gutiérrez C G. 2007. A single dose of bovinesomatotropin 5 days before the end of progestin-based estrous synchronization increase proliûcacy in sheep. Animal Reproduction Science 102: 31–37. DOI: https://doi.org/10.1016/j.anireprosci.2006.09.024

Chi M Y, Schlein A L and Moley K H. 2000. High insulin-like growth factor 1 (IGF-1) and insulin concentration trigger apoptosis in the mouse blastocyst via down-regulation of the IGF-1 receptor. Endocrinology 141: 4784–92. DOI: https://doi.org/10.1210/endo.141.12.7816

Driancourt M A and Disenhaus C. 1997. Lack of effects of growth hormone administration on ovarian function of lactating goats. Animal Reproduction Science 46: 123–32. DOI: https://doi.org/10.1016/S0378-4320(96)01608-9

Folch J, Ramon J P, Cocero M J, Alabart J L and Beckers J F. 2001. Exogenous growth hormone improves the number of transferable embryos in superovulated ewes. Theriogenology 55: 1777–85. DOI: https://doi.org/10.1016/S0093-691X(01)00520-9

Fouladi-Nashta A A and Campbell K H S. 2006. Dissociation of oocyte nuclear and cytoplasmic maturation by the addition of insulin in cultured bovine antralfollicles. Reproduction 131: 449–60. DOI: https://doi.org/10.1530/rep.1.00581

Fouladi-Nashta A A, Gutierrez C G, Gong J G, Garnsworthy P C and Webb R. 2007. Impact of dietary fatty acids on oocyte quality and development in lactating dairy cows. Biology of Reproduction 77: 9–17. DOI: https://doi.org/10.1095/biolreprod.106.058578

Gong J G, Campbell B K, Bramley T A and Webb R. 1996. Treatment with recombinant bovine somatotropinenhances ovarian follicle development and increases the secretion of insulin-like growth factor-I by ovarian follicles in ewes. Animal Reproduction Science 41: 13–26. DOI: https://doi.org/10.1016/0378-4320(95)01437-3

Hasler J F, Bilby C R, Collier R J, Denham S C and Lucy M C. 2003. Effect of recombinant bovine somatotropin on superovulatory response and recipient pregnancy rates in a commercial embryo transfer program. Theriogenology 59: 1919–28. DOI: https://doi.org/10.1016/S0093-691X(02)01295-5

Joyce I M, Khalid M and Haresign W. 1998. Growth hormone priming as an adjunct treatment in superovulatory protocols in the ewe alters follicle development but has no effect on ovulation rate. Theriogenology 50: 873–84. DOI: https://doi.org/10.1016/S0093-691X(98)00192-7

Lee H J, Hwang S and Yoon J T. 2007. Effects of bovine somatotropin (bST)administration combined with controlled internal drug release (CIDR) on embryo quality and pregnancy of Hanwoo (Korean Native Beef Cattle) during commercial embryo transfer program. Asian-Australasian Journal of Animal Sciences 20 (2): 194–99. DOI: https://doi.org/10.5713/ajas.2007.194

Martinez A M, Gutiérrez C G, Domínguez H Y M and Hernández C J. 2011. Estrous response and pregnancy rate in seasonal anoestrous goats treated with progestogens and bovine somatotropin. Revista Mexicana de Ciencias Pecuarias 2: 221– 27.

Mejia O, Palma-Irizarry M, Rosas J, Madrid-Marina V, Valencia M J and Zarco L. 2012. Administration of recombinant bovine somatotropin (rsBT) at the time of breeding in superovulated fertile and subfertile ewes. Small Ruminant Research 102: 51– 56. DOI: https://doi.org/10.1016/j.smallrumres.2011.09.016

Mihalik J, Rehák P and Koppel J. 2000. The inûuence of insulinon thein-vitro development ofmouse and bovine embryos. Physiological Research 49: 347–54.

Montero-Pardo A, Hernández-Céron J, Rojas-Maya S, Valencia J, Rodríguez-Cortez A and Gutiérrez C G. 2011. Increased cleavage and blastocyst rate in ewes treated with bovine somatotropin 5 days before the end of progestin-based estrous synchronization. Animal Reproduction Science 125: 69–73. DOI: https://doi.org/10.1016/j.anireprosci.2011.03.004

Moreira F, Badinga L, Burney C and Thatcher W W. 2002. Bovine somatotropin increases embryonic development in superovulated cows and improves post-transfer pregnancy rates when given to lactating recipient cows. Theriogenology 57: 1371–87. DOI: https://doi.org/10.1016/S0093-691X(01)00719-1

Navarrete-Sierra L F, Cruz-Tamayo AA, González-Parra E I, Pina- Aguilar R E, Sangines-García J R, Toledo-López V and Ramón-Ugalde J P. 2008. Effect of recombinant growth hormone (rbST) application on superovulatory response and embryo viability in hair ewes. Revista Cientifica 18: 175–79.

Neira J A, Tainturier D, Pena M A and Martal J. 2010. Effect of the association of IGF-I, IGF-II, bFGF.TGF-1,GM-CSF, and LIF on the development of bovine embryos produced in vitro. Theriogenology 73: 595–604. DOI: https://doi.org/10.1016/j.theriogenology.2009.10.015

Neves E F, Ramos A F and Marques J A P. 2005. Pre- tratamentocom somatotropinabovina (rBST) nasuperovulaòão de doadorasda raòaHolandesa. Arquivo Brasileiro de Medicina Veterinária 57: 205–09. DOI: https://doi.org/10.1590/S0102-09352005000200011

Oliveira M E F. 2011. State of the art in the superovulation of ewes. Acta Scientiae Veterinariae 39 (Suppl. 1): 29–35.

Ribeiro E S, Bruno R G S, Farias A M, Hernández-Rivera J A, Gomes G C, Surjus R, Becker L F V, Birt A, Ott T L, Branen J R, Sasser R G, Keisler D H, Thatcher W W, Bilby T R and Santos J E P. 2014. Low doses of bovine somatotropin enhance conceptus development and fertility in lactating dairy cows. Biology of Reproduction 90: 1–12. DOI: https://doi.org/10.1095/biolreprod.113.114694

Scaramuzzi R J, Brown H M and Dupont J. 2010. Nutritional and metabolic mechanisms in the ovary and their role in mediating the effects of diet on folliculogenesis: A perspective. Reproduction Domestic Animal 45 (Suppl.3): 32–41. DOI: https://doi.org/10.1111/j.1439-0531.2010.01662.x

Spencer, G S G, Schurmann A, Berry C, Wolff J E, Napier J R, Hodgkinson S C and Bass J J. 1994. Comparison of the effects of recombinant ovine, bovine and porcine growth hormones on growth, efûciency and carcass characteristics in lambs. Livestock Production Science 37: 311–21. DOI: https://doi.org/10.1016/0301-6226(94)90125-2

Stringfellow D A and Seidel G E. 2000. Manual of the International Embryo Transfer Society (IETS), 3rd Ed. International Embryo Transfer Society, Savory, IL, United States, Pp. 175–78.

Velazquez M A, Hadeler K G, Herrmann D, Kues W A, Rémy B, Beckers J F and Niemann H. 2012. In-vivo oocyte IGF-1 priming increases inner cell mass proliferation of in-vitro- formed bovine blastocysts. Theriogenology 78: 517–27. DOI: https://doi.org/10.1016/j.theriogenology.2012.02.034

Velazquez M A, Hermann D, Kues W A and Niemann H. 2011. Increased apoptosis in bovine blastocysts exposed to high levels of IGF1 is not associated with down regulation of the IGF1 receptor. Reproduction 141: 91–103. DOI: https://doi.org/10.1530/REP-10-0336

Velazquez M A, Zaraza J, Oropeza A, Webb R and Niemann H. 2009. The role of IGF1 in the in-vivo production of bovine embryos from super-ovulated donors. Reproduction 137: 161– 80. DOI: https://doi.org/10.1530/REP-08-0362

Downloads

Submitted

2016-06-15

Published

2016-06-16

Issue

Section

Articles

How to Cite

SAFDAR, A. H. A. (2016). Superovulatory responsiveness and embryonic development in Iranian Afshari ewes treated with two different concentrations of bovine somatotropin. The Indian Journal of Animal Sciences, 86(6), 659–664. https://doi.org/10.56093/ijans.v86i6.59190
Citation