Souza F F, Martins J L A, Afolabi O O, Paranzini C S, Leme D P, Silva M S O M, Daros V F, Chirinéia V H, Lopes M D
Department of Veterinary Surgery and Animal Reproduction, School of Veterinary Medicine and Animal Science, São Paulo State University, UNESP, Botucatu, São Paulo, Brazil.
Department of Veterinary Surgery and Animal Reproduction, School of Veterinary Medicine and Animal Science, São Paulo State University, UNESP, Botucatu, São Paulo, Brazil.
Cryobiology. 2025 Sep;120:105297. doi: 10.1016/j.cryobiol.2025.105297. Epub 2025 Sep 1.
This study aimed to describe the cells of the seminiferous epithelium collected by fine needle aspiration cytology (FNAC), reproductive tract observations, semen collection, and sperm cryopreservation from coatis (Nasua nasua). Seven adult coatis were anesthetized, the reproductive tract was examined, and semen was collected by electroejaculation and cryopreserved using an extender based on protocol for domestic dogs, except that prior to cryopreservation, no centrifugation to remove the seminal plasma was performed. Testicular FNAC was also performed on each testis. The germ cells of seminiferous epithelium were identified and had cell characteristics similar to other species except for the secondary spermatocyte which was not present. Semen samples were collected from four animals, three of which were suitable for cryopreservation, although their seminal characteristics slightly declined after freezing. Examination of the coati reproductive tract revealed well developed penile bone and preputial glands like other carnivores. The testicular length x width x height meant 2.13 × 1.7 × 1.7 cm and testicular volume meant 4.5 cm. The sperm morphology of coati exhibited an angular head shape, which was evident in the membrane integrity fluorescence assessment. The sperm motility was between 20 and 70 %, and the concentration was between 14 and 129 × 10 sperm/mL with motility of 30.0 ± 17.32 % vs 23.33 ± 11.55 % between samples thawed at 46 °C/15s and 37 °C/30s. In conclusion, testicular FNAC can be a useful tool for evaluating testicular function based on sperm production. Our findings demonstrate that semen collection and cryopreservation in coatis can be achieved using electroejaculation, extenders, and cryopreservation protocols similar to those used for domestic dogs. While these results provide a template for semen cryopreservation in other Procyonidae species, further investigation is needed to determine the necessity of removing seminal plasma.
本研究旨在描述通过细针穿刺细胞学检查(FNAC)、生殖道观察、精液采集以及浣熊(南美浣熊)精子冷冻保存所采集的生精上皮细胞。对7只成年浣熊进行麻醉,检查其生殖道,并通过电刺激射精采集精液,按照家犬的方案使用稀释液进行冷冻保存,但在冷冻保存前未进行离心去除精浆操作。同时对每个睾丸进行睾丸FNAC检查。生精上皮的生殖细胞已被识别,除不存在次级精母细胞外,其细胞特征与其他物种相似。从4只动物采集了精液样本,其中3只适合冷冻保存,不过冷冻后其精液特征略有下降。对浣熊生殖道的检查发现,其阴茎骨和包皮腺发育良好,与其他食肉动物类似。睾丸的长×宽×高平均为2.13×1.7×1.7厘米,睾丸体积平均为4.5立方厘米。浣熊的精子形态呈角状头部,这在膜完整性荧光评估中很明显。精子活力在20%至70%之间,浓度在14至129×10⁶精子/毫升之间,46°C/15秒解冻样本与37°C/30秒解冻样本之间的活力分别为30.0±17.32%和23.33±11.55%。总之,睾丸FNAC可作为基于精子生成评估睾丸功能的有用工具。我们的研究结果表明,使用与家犬相似的电刺激射精、稀释液和冷冻保存方案,可实现浣熊精液的采集和冷冻保存。虽然这些结果为其他浣熊科物种的精液冷冻保存提供了模板,但仍需进一步研究以确定去除精浆的必要性。