This study aimed to evaluate the effect of treatment with equine chorionic gonadotrophin (eCG) on the follicular dynamics and function of crossbred cows with different circulating progesterone (P4) concentrations during synchronization of ovulation in a fixed-time artificial insemination (FTAI) protocol. To this end, 30 crossbred cows were submitted to a pre-synchronization protocol to ensure that all of them presented corpus luteum (CL) at the beginning of the protocol, and were evaluated by transrectal ultrasonography (TRUS) to verify the presence of CL. After that, the animals underwent an ovulation synchronization protocol and evaluation of follicular dynamics and vascularization by B-mode and power-Doppler ultrasound (US). High plasma P4 concentrations at the time of ovulation synchronization negatively influenced follicle diameter on day 10 (D10), preovulatory follicle diameter, and preovulatory follicle wall vascularization area (p<0.05). Cows with high P4 concentration at the time of ovulation synchronization that were treated with eCG showed follicle diameter on D10 and preovulatory follicle diameter and wall vascularization area (p>0.05) similar to those of animals with low P4 concentration at the time of ovulation synchronization. Therefore, high P4 concentrations at the time of ovulation synchronization negatively influence follicular diameter and vascularization, and eCG can be used as a strategy to favor better follicular and luteal response in crossbred cows with high P4 concentrations submitted to an FTAI protocol.
Cooling and freezing processes cause physical and chemical damage to sperm by cold shock and oxidative stress. This study aimed to evaluate the effect of two antioxidants on sperm parameters of cooled and frozen-thawed ram semen diluted in an egg yolk-based extender. Semen was collected from 30 rams and processed in two consecutive experiments to test the inclusion of different concentrations of quercetin and butylated hydroxytoluene (BHT) in an egg yolk-based semen extender. Dimethyl sulfoxide (DMSO) was added as a solvent to the semen extender in a ratio of 1 mL DMSO for 90 mg of quercetin and 1 mL DMSO for 880 mg of BHT. After collection, semen was diluted at 200 × 106 motile sperm/mL (control) and split into different groups in each experiment. In experiment 1, semen was diluted with the extender containing quercetin (Q5, 5 μg/mL; Q10, 10 μg/mL; Q15, 15 μg/mL) or DMSO alone (DMSO1, 0.055 μL DMSO per mL; DMSO2, 0.165 μL DMSO per mL). In experiment 2, semen was diluted with the extender with BHT (BHT1, 0.5 μg/mL; BHT2, 1 μg/mL; BHT3, 1.5 μg/mL) or DMSO alone (DMSO3, 0.375 μL DMSO per mL; DMSO4, 1.125 μL DMSO per mL). After dilution, the semen was divided into two aliquots. Treated ram sperm samples were also subjected to different storage methods. The first set of samples was cooled at 5 °C for 24 h, whereas the second set of samples was frozen-thawed. Sperm motility parameters and plasma membrane integrity (PMI) were evaluated immediately after dilution (0h) and 24 h after cooling and in the frozen-thawed samples via computer-assisted sperm analysis and epifluorescence microscopy, respectively. The inclusion of quercetin or BHT did not affect sperm motility parameters or PMI of fresh, cooled, or frozen-thawed sperm in this study (P < 0.05). However, further studies are needed to test the effects of these antioxidants on the fertility of cryopreserved ram semen.
Although stem cell therapy is a promising alternative for treatment of degenerative diseases, there are just few reports on the use of stem cells therapy in horse's reproductive system. This study aims to evaluate the effect of intratesticular injection of bone marrow mesenchymal stromal/stem cells (MSCs) in healthy stallions, and its outcome on seminal parameters and fertility. In Experiment 1, 24 stallions were divided into treatment group (TG) and control group (CG). In the TG, an intratesticular application of MSC was performed, and in the CG, only PBS was used.Measurements of testicular volume, surface temperature and Doppler ultrasonography were performed 24 and 48 hr after treatments. Fifteen days after application, the testicles were removed and submitted to histological analysis. In Experiment 2, 3 fertile stallions received similarly treatment with MSCs. Physical examination and sperm analysis were performed weekly during 60 days after treatment, and at the end, semen from one of them was used for artificial inseminations of 6 healthy mares.In Experiment 1, clinical examinations showed no signals of acute inflammation on both groups according to the analysed variables (p > .05). Also, no signal of chronic inflammation was observed on histological evaluation. In Experiment 2, stallions presented no physical alterations or changes in sperm parameters, and a satisfactory fertility rate (83%; 5/6) was observed after AI. The results support the hypothesis that intratesticular application of bone marrow MSCs is a safe procedure, and this could be a promising alternative to treat testicular degenerative conditions. K E Y W O R D S cell therapy, equine, injection, testicle 430 | PAPA et Al.
As aderências congênitas estão presentes desde o nascimento como anomalia embriológica no desenvolvimento da cavidade peritoneal. O presente trabalho teve por objetivo relatar o caso de aderência congênita de uma cadela da raça Yorkshire de 9 meses submetida ao porcedimento de ovariosalpingohisterectomia (OSH) eletiva. Na anamnese a proprietária relatou que o animal nunca foi submetido a nenhum procedimento cirúrgico e seu estado fisiológico estava dentro da normalidade. No exame clínico não foi observado nenhuma alteração nos parâmetros (frequência cardíaca, frequência respiratória, temperatura, tempo de preenchimento capilar, escore corporal, linfonodos, assim como palpação abdominal e auscultação cardiopulmonar) do animal, assim como nos exames laboratoriais (Hemograma, ALT, FA, Ureia e creatinina). Sendo assim, o animal foi encaminhado e posteriormente submetido ao procedimento cirúrgico, durante a laparotomia exploratória foi identificado a aderência ovário-intestinal. Foi realizado a correção cirúrgica (adesiólise), sem complicação durante o procedimento.
ResumoEste estudo teve por objetivo comparar o número de folículos aspirados, oócitos recuperados, qualidade e viabilidade oocitária entre ovelhas das raças Dorper e Santa Inês, submetidas à aspiração folicular por vídeolaparoscopia. Para realização deste estudo, foram efetuadas 118 aspirações foliculares, das quais 65 foram realizadas em ovelhas da raça Dorper e 53 em ovelhas da raça Santa Inês. Os resultados encontrados para as ovelhas Dorper foram 28,31 ± 17,42 folículos/ovelha, 12,21 ± 6,74 oócitos/ovelha, taxa de recuperação de 47,9% e 8,93 ± 5,25 oócitos viáveis/ovelha. Para as ovelhas Santa Inês foram, 22,14 ± 16,08 folículos/ovelha, 12,64 ± 8,29 oócitos/ovelha, taxa de recuperação de 55% e 8,92 ± 6,58 oócitos viáveis/ovelha. Não houve influência das raças sobre o número de folículos aspirados, oócitos recuperados, taxa de recuperação, qualidade e viabilidade oocitária em aspiração folicular por vídeolaparoscopia. Palavras-chave: folículo; oócito; ovino. AbstractThis study aimed to compare the number of aspirated follicles, recovered oocytes, oocyte quality and viability between Dorper and Santa Inês ewes submitted to the videolaparoscopic ovum pick-up. To conduct this study, 118 follicular aspirations were performed, of which 65 were performed in Dorper ewes and 53 in Santa Ines ewes. The results for Dorper sheep were 28.31 ± 17.42 follicles/ewe, 12.21 ± 6.74 oocytes/ewe, recovery rate of 47.9% and 8.93 ± 5.25 viable oocytes/ewe. For Santa Inês ewes the results were 22.14 ± 16.08 follicles/ewe, 12.64 ± 8.29 oocytes/ewe, recovery rate of 55% and 8.92 ± 6.58 viable oocytes/ewe. There was no influence of breed on the number of aspirated follicles, recovered oocytes, recovery rate, oocyte quality and viability in videolaparoscopic ovum pick-up.
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