Autologous seminal plasma and post-breeding uterine lavage as alternative options to improve fertility rates of jennies inseminated with cryopreserved jack semen
P.V.L.F. Oliveira , L.G.T.M. Segabinazzi , A.M. Crespilho , J.V. Oliveira , A.C. Silva , C.P. Freitas-Dell’Aqua , J.A. Dell’Aqua Jr , F.O. Papa
{"title":"Autologous seminal plasma and post-breeding uterine lavage as alternative options to improve fertility rates of jennies inseminated with cryopreserved jack semen","authors":"P.V.L.F. Oliveira , L.G.T.M. Segabinazzi , A.M. Crespilho , J.V. Oliveira , A.C. Silva , C.P. Freitas-Dell’Aqua , J.A. Dell’Aqua Jr , F.O. Papa","doi":"10.1016/j.jevs.2025.105613","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Poor fertility of cryopreserved semen remains a challenge in donkeys.</div></div><div><h3>Aims/objectives</h3><div>This study evaluated strategies to enhance fertility of cryopreserved semen in donkeys.</div></div><div><h3>Methods</h3><div>Experiment 1 assessed <em>in vitro</em> parameters of semen cryopreserved with two freezing-semen protocols (BC and mINRA). For evaluation, samples were thawed and split into two aliquots: one served as a control, and the second was re-extended with seminal plasma (SP). Sperm motility, plasma membrane and acrosome integrity (PMAI), lipid peroxidation (LPO), and hydrogen peroxide (H₂O₂) were analyzed. Experiment 2 involved 86 estrous cycles of 33 jennies, inseminated with semen cryopreserved using BC (n = 43 cycles) or mINRA (n = 43 cycles). Each group included control cycles (BC, n = 10; mINRA, n = 10) and three treatments: SP, frozen-thawed semen re-extended in SP (BC, n = 08; mINRA, n = 08); UL, uterine lavage (UL) 10 h post-AI (BC, n = 11; mINRA, n = 11); and SP+UL, frozen-thawed semen re-extended in SP followed by UL 10 h post-AI (BC, n = 14; mINRA, n = 14).</div></div><div><h3>Results</h3><div>Post-thaw motility was similar between cryopreservation protocols (P > 0.05), but adding SP reduced the motility parameters of cryopreserved semen (P < 0.05). PMAI was higher, and LPO and H<sub>2</sub>O<sub>2</sub> were lower in semen cryopreserved using BC (P < 0.05). Seminal plasma addition did not affect PMAI but reduced LPO and H<sub>2</sub>O<sub>2</sub> (P < 0.05). Pregnancy rates did not differ between semen cryopreserved using BC (21 %) and mINRA (23 %; P > 0.05). The SP+UL-assigned cycles had higher fertility rates (43 %; P = 0.01) compared to control-assigned cycles (0/20), whereas SP- (13 %) and UL-cycles (23 %) had intermediate pregnancy rates (P > 0.05).</div></div><div><h3>Conclusion</h3><div>Cryopreservation protocol did not impact sperm quality or fertility. However, the association of semen re-extension in SP and post-insemination UL improved fertility outcomes in jennies.</div></div>","PeriodicalId":15798,"journal":{"name":"Journal of Equine Veterinary Science","volume":"150 ","pages":"Article 105613"},"PeriodicalIF":1.6000,"publicationDate":"2025-05-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Equine Veterinary Science","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0737080625002710","RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"VETERINARY SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Background
Poor fertility of cryopreserved semen remains a challenge in donkeys.
Aims/objectives
This study evaluated strategies to enhance fertility of cryopreserved semen in donkeys.
Methods
Experiment 1 assessed in vitro parameters of semen cryopreserved with two freezing-semen protocols (BC and mINRA). For evaluation, samples were thawed and split into two aliquots: one served as a control, and the second was re-extended with seminal plasma (SP). Sperm motility, plasma membrane and acrosome integrity (PMAI), lipid peroxidation (LPO), and hydrogen peroxide (H₂O₂) were analyzed. Experiment 2 involved 86 estrous cycles of 33 jennies, inseminated with semen cryopreserved using BC (n = 43 cycles) or mINRA (n = 43 cycles). Each group included control cycles (BC, n = 10; mINRA, n = 10) and three treatments: SP, frozen-thawed semen re-extended in SP (BC, n = 08; mINRA, n = 08); UL, uterine lavage (UL) 10 h post-AI (BC, n = 11; mINRA, n = 11); and SP+UL, frozen-thawed semen re-extended in SP followed by UL 10 h post-AI (BC, n = 14; mINRA, n = 14).
Results
Post-thaw motility was similar between cryopreservation protocols (P > 0.05), but adding SP reduced the motility parameters of cryopreserved semen (P < 0.05). PMAI was higher, and LPO and H2O2 were lower in semen cryopreserved using BC (P < 0.05). Seminal plasma addition did not affect PMAI but reduced LPO and H2O2 (P < 0.05). Pregnancy rates did not differ between semen cryopreserved using BC (21 %) and mINRA (23 %; P > 0.05). The SP+UL-assigned cycles had higher fertility rates (43 %; P = 0.01) compared to control-assigned cycles (0/20), whereas SP- (13 %) and UL-cycles (23 %) had intermediate pregnancy rates (P > 0.05).
Conclusion
Cryopreservation protocol did not impact sperm quality or fertility. However, the association of semen re-extension in SP and post-insemination UL improved fertility outcomes in jennies.
期刊介绍:
Journal of Equine Veterinary Science (JEVS) is an international publication designed for the practicing equine veterinarian, equine researcher, and other equine health care specialist. Published monthly, each issue of JEVS includes original research, reviews, case reports, short communications, and clinical techniques from leaders in the equine veterinary field, covering such topics as laminitis, reproduction, infectious disease, parasitology, behavior, podology, internal medicine, surgery and nutrition.