Abstract
Twenty-eight pluriparous and non-lactating Santa Inês sheep were synchronized with vaginal sponge and an intramuscular (IM) injection of 37.5 μg of cloprostenol on random days of the estrous cycle (D0); day 6 (D6), at 7:00 am, the devices were removed, and after 24 h (D7), GnRH analog (25 μg of lecirelin) was administrated. Fixed-time artificial insemination (FTAI) with cervical traction by the transcervical route was performed 52 to 58 h after sponge removal. Doppler velocimetry of both uterine arteries was performed on D0, D2, D4, and the morning of D6 (every 48 h), and then every 12 h from D6 to D8 (7:00 a.m. and 7:00 p.m.). We analyzed the peak systolic velocity (PSV), end-diastolic velocity (EVD), time-averaged maximum and mean velocity (TAMAX, TAMEAN), pulsatility index (PI), resistance index (RI), systolic/diastolic ratio (S/D), arterial diameter (AD), and blood flow volume (BFV), with the objective of evaluating the hemodynamic behavior of blood flow velocity parameters of the uterine artery during a short-term progesterone synchronization protocol in ewes. With respect to phases, we noted increases in the means of TAMAX and TAMEAN and decreases of EDV, PI, and RI (P < 0.05). S/D, EDV, TAMEAN, PI, RI, SD, AD, and BFV showed differences between the time of progesterone insertion and the estimated time of ovulation (which was considered the last evaluation) (P < 0.05). The PI and RI values were different when comparing the times of insertion and withdrawal of the progesterone device (PI 2.53–1.54 and RI 0.76–0.68) (P < 0.05). The PI was different with respect to side (P < 0.001), but no side effect was seen in the RI. In conclusion, the two uterine arteries behave differently under the effect of progesterone (intravaginal sponges) and the effect of estradiol during the follicular phase, and estrous phase was responsible for increasing uterine blood flow.
Similar content being viewed by others
References
Achiron, R., Goldenberg, M., Lipitz., Mashiach, S., 1993. Transvaginal duplex Doppler ultrasonography in bleeding patients suspected of having residual trophoblastic tissue. Obstetrics and Gynecology. 81, 507–511.
Alcazar, J.L., 1998. Transvaginal ultrasonography combined with color velocity imaging and pulsed Doppler to detect residual trophoblastic tissue. Ultrasound in Obstetrics and Gynecology. 11, 54–58.
Arruda, R.P., Celeghini, E.C.C., Garcia, A.R., Carli dos Santos, G., Leite, T.C., Oliveira, L.Z., et al., 2015. Bull sperm morphology: interpretation and impact on fertility. Revista Brasileira de Reprodução Animal. 39 (1), 47–60.
Beltrame, R.T., Covre, C., Littig, L.B., Martins, A.B., Quirino, C.R., Junior, A.B., et al., 2017. Transrectal Doppler sonography of uterine blood flow in ewes during pregnancy. Theriogenology 91, 55–61.
Blanco, P. G, Rodríguez, R., Rube, A., Arias, D.O., Tórtora, M., Díaz, J.D., et al., 2011. Doppler ultrasonographic assessment of maternal and fetal blood flow in abnormal canine pregnancy. Animal Reproduction Science 126, 130–135.
Bollwein, H., Baumgartner, U., Stolla, R., 2002 Transrectal Doppler sonography of uterine blood flow in cows during pregnancy. Theriogenology 57 (8), 2053–2061.
Esmaeillou, H., Jamal, A., Eslamian, L., Marsousi, V., Sarvi, F., Kokab, A., 2015. Accurate Detection of Retained Products of Conceptions after First- and Second- trimester Abortion by Color Doppler. Journal of Medical Ultrasound. 23, 34–38.
Ferreira, A.M., Pires, C.R., Moron, A.F., Araujo Júnior, E., Traina, E., Mattar, R., 2007. Doppler assessment of uterine blood flow in recurrent pregnancy loss. International Journal of Gynecology. Obstet. 98, 115–119.
Ferrusola, C.O., Gracia-Calvo, L.A., Ezquerra, J., Peña, F.J., 2014 Use of Colour and Spectral Doppler Ultrasonography in Stallion Andrology. Reproduction in Domestic Animals. 49 (4), 88–96.
Ginther, O.J., 2014. How ultrasound technologies have expanded and revolutionized research in reproduction in large animals. Theriogenology 81, 112–125.
Ginther, O.J., Gastal, E.L., Gastal, M.O., Utt, M.D., Beg, M.A., 2007. Luteal blood flow and progesterone production in mares. Animal Reproduction Science. 99. 213–220.
Herzog, K., Bollwein, H., 2007. Application of Doppler ultrasonography in cattle reproduction. Reproduction in Domestic Anim. 42 (Suppl 2), 51–58.
Idowu, B.M., Ibitoye, B.O., Adetiloye, V.A., 2017. Uterine Artery Doppler Velocimetry of Uterine Leiomyomas in Nigerian Women. Rev. Bras. Ginecol. Obstet. 39, 464–470.
Köster, K., Poulsen, C.N., Günzel-Apel, A.R., 2001. A Doppler ultrasonographic study of cyclic changes of ovarian perfusion in the Beagle bitch. Reproduction 122, 453–461.
Lucy, M.C., 2007. The bovine dominant ovarian follicle . J.Anim. Sci. 85, E89–E99.
Marques Júnior, A.P., Martins, T.M. Borges Á.M., 2011. Diagnosis and treatment of uterine infection in cows. Rev. Bras. Reprod. Anim. 35 (2), 293–298.
Mattioli, M., Barboni, B., Turriani, M., Galeati, G., Zannoni, A., Castellani, G., et al., 2001. Follicle activation involves vascular endothelial growth factor production and increased blood vessel extension. Biol. Reprod. 65, 1014–1019.
Menchaca, A., Santos Neto, P.C., Cuadro, F., 2017. Estrous synchronization treatments in sheep: Brief update. Rev. Bras. Reprod. Anim. 41 (1), 340–344.
Ortiz-Rodriguez, J.M., Lopez, L.A., Muñoz, P.M., Alvarez, M., Phillips, G.G., Anel, L., et al., 2017. Pulse Doppler ultrasound as a tool for the diagnosis of chronic testicular dysfunction in stallions. Plos One. 12(5),1–21.
Panarace, M., Garnil, C., Marfil, M., Jauregui, G., Lagioia, J., Luther, E., et al., 2006. Transrectal Doppler sonography for evaluation of uterine blood flow throughout pregnancy in 13 cows. Theriogenology 66 (9), 2113–2119.
Petridis, I.G., Barbagianni, M.S., Ioannidi, K.S., Samaras, E., Fthenakis, G.C., Vloumidi, E.I., 2017. Doppler ultrasonographic examination in sheep. Small Ruminant Res. 152, 22–32.
Pinggera, G.M., Mitterberger, M., Bartsch, G., Strasser, H., Gradl, J., Aigner, F., et al., 2008. Assessment of the intra- testicular resistive index by colour Doppler ultrasonography measurements as a predictor of spermato- genesis. BJU Int. 101(6), 722–726.
Rawy, M., Mido, S., El-Sheikh Ali, H., Derar, D., Megahed, G., Kitahara, G., et al. 2018. Effect of exogenous estradiol Benzoate on uterine blood flow in postpartum dairy cows. Anim. Reprod. Sci. 192, 136–145.
Russi, L.S., Costa-e-Silva, E.V., Zúccari, C.E.S.N., Recalde, C.S., 2010. Human resources in artificial insemination of beef cattle: profile of managers and inseminators. Rev. Bras. Zootecn. 39(7), 1464–1470.
Saunders, H.S., Burns, P.N., Needleman, L,. Liu, J.B., Boston, R. Wortman, J.A., Chan, L., 1998. Hemodynamic factors affecting uterine artery Doppler waveform pulsatility in sheep. J Ultrasound Med. 17, 357–68.
Sprague, B.J., Phernetton, T. M., Magness, R. R., & Chesler, N. C. (2009). The effects of the ovarian cycle and pregnancy on uterine vascular impedance and uterine artery mechanics. European journal of obstetrics, gynecology, and reproductive biology, 144 Suppl 1(Suppl 1), S170–S178. doi:https://doi.org/10.1016/j.ejogrb.2009.02.041
Acknowledgments
This study was conducted as a requirement of junior scientific initiation (Federal Institute of Espírito Santo - IFES), scientific initiation, and graduation work for the Veterinary course at the Centro Universitário do Espírito Santo (UNESC).
Funding
We had financial support (TO 913/2015) and a scholarship financed by Fundação de Amparo a Pesquisa e Inovação do Espírito Santo (FAPES). Joao Vitor Pagoto Careta has a scholarship financed by FAPES, which is gratefully acknowledged.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Statement of animal rights
This study was approved by the institute’s ethics committee (Protocol No. CEUA/IFES – ES 23147.000841-2016-23).
Conflict of interest
The authors declare that they have no conflict of interest.
Additional information
Publisher’s note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Highlights
• The Doppler parameters and the diameter of the uterine artery showed significant changes during a short synchronization protocol
• Differences were found between the means of the Doppler parameters in relation to the phase of the protocol (progesterone × estradiol)
• Doppler parameters and the diameter of the uterine artery showed significant correlations
Rights and permissions
About this article
Cite this article
Beltrame, R.T., Morais Junior, N.N., Careta, J.V.P. et al. Uterine hemodynamics during a short-term progesterone synchronization protocol in ewes. Trop Anim Health Prod 52, 503–509 (2020). https://doi.org/10.1007/s11250-019-02035-5
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11250-019-02035-5