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热休克蛋白 HSPA8 添加到冷冻保护剂中可提高棕熊(Ursus arctos)精子在冷藏和解冻后的存活率。

The addition of heat shock protein HSPA8 to cryoprotective media improves the survival of brown bear (Ursus arctos) spermatozoa during chilling and after cryopreservation.

机构信息

ITRA-ULE, INDEGSAL, University of León, León, Spain.

出版信息

Theriogenology. 2013 Feb;79(3):541-50. doi: 10.1016/j.theriogenology.2012.11.006. Epub 2012 Dec 11.

Abstract

The Cantabrian brown bear survives as a small remnant population in northern Spain and semen cryopreservation for future artificial insemination is one of the measures being implemented for conservation of this species. As part of this program we investigated the value of adding heat shock protein A8 (HSPA8) to media (N-[Tris(hydroxymethyl)methyl]-2-aminoethanesulfonic acid-TRIS-fructose with 20% egg yolk) used for chilling and cryopreserving the spermatozoa. Semen samples from eight brown bears were obtained by electroejaculation during the breeding season. In experiment 1, we tested three concentrations of HSPA8 (0.5, 1, and 5 μg/mL) to determine whether sperm motility (computer assisted sperm analysis system) and sperm survival could be improved during refrigeration (5 °C) up to 48 hours. Results showed that sperm viability (test with propidium iodide) was improved by the addition of 0.5 and 5 μg/mL HSPA8. In experiment 2, HSPA8 was added to the cryopreservation media (6% final glycerol concentration) before the freezing process. Though there were no differences in sperm viability immediately after thawing (analyses to 0 hours), plasma membrane permeability (test with YO-PRO-1) was significantly lower by the presence of HSPA8 (1 μg/mL) and acrosomal damage (test with peanut agglutinin-fluorescein isothiocyanate conjugate) was reduced by higher concentrations of HSPA8 (1 and 5 μg/mL) (analyses after thermal stress test incubating over 2 hours to 37 °C). In experiment 3, results of a simple progression test carried out through artificial mucus (hyaluronic acid 4 mg/mL) showed a significant decrease in the total number of sperm able to swim a distance of 0.5 to 2 cm through a capillary tube for all HSPA8-based extenders. Nevertheless, the distance traveled by the vanguard spermatozoa, which represent a highly motile subpopulation, was restored by the inclusion of 1 and 5 μg/mL HSPA8 in the cryopreservation media. Thus, the HSPA8 addition to extender improves the quality of brown bear (Ursus arctos) sperm during chilling (viability) and after cryopreservation (number of sperm with damaged acrosomes and "apoptotic-like" changes).

摘要

坎塔布连棕熊作为一个小的残余种群生活在西班牙北部,精液的冷冻保存,以便未来进行人工授精,是保护该物种的措施之一。作为该计划的一部分,我们研究了在用于冷却和冷冻保存精子的培养基(N-[三(羟甲基)甲基]-2-氨基乙磺酸-TRIS-果糖,含 20%卵黄)中添加热休克蛋白 A8(HSPA8)的价值。在繁殖季节,通过电刺激法从 8 只棕熊中获得精液样本。在实验 1 中,我们测试了 HSPA8 的三种浓度(0.5、1 和 5μg/mL),以确定在冷藏(5°C)期间是否可以通过添加 HSPA8 来提高精子活力(计算机辅助精子分析系统)和精子活力持续时间长达 48 小时。结果表明,添加 0.5 和 5μg/mL HSPA8 可提高精子活力(用碘化丙啶检测)。在实验 2 中,在冷冻过程之前将 HSPA8 添加到冷冻保存培养基(最终甘油浓度为 6%)中。尽管在解冻后立即进行的精子活力分析(分析至 0 小时)中没有差异,但存在 HSPA8 时质膜通透性(用 YO-PRO-1 检测)显著降低(通过热应激试验孵育超过 2 小时至 37°C),并且 HSPA8 浓度较高时(1 和 5μg/mL)顶体损伤(用花生凝集素-荧光素异硫氰酸酯结合物检测)减少。在实验 3 中,通过人工黏液(透明质酸 4mg/mL)进行的简单运动能力测试的结果表明,所有基于 HSPA8 的延伸剂中,能够游过 0.5 至 2cm 长的毛细管的精子总数显著减少。然而,通过在冷冻保存培养基中添加 1 和 5μg/mL HSPA8,可以恢复前导精子的游动距离,前导精子代表一个高度活跃的亚群。因此,HSPA8 的添加可以提高棕熊(Ursus arctos)精子在冷却(活力)和冷冻保存后的质量(顶体受损的精子数量和“凋亡样”变化)。

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