Department of Veterinary Gynaecology and Obstetrics, Bihar Veterinary College, Bihar Animal Sciences University, Patna, 800014, India.
Dean Bihar Veterinary College, Bihar Animal Sciences University, Patna, 800014, India.
Cryobiology. 2024 Sep;116:104931. doi: 10.1016/j.cryobiol.2024.104931. Epub 2024 Jul 10.
Cryopreservation of goat spermatozoa is challenging due to several factors, including one of the most essential, i.e., oxidative stress. It is particularly essential in goat semen due to its scanty ejaculate volume and high sperm concentration. This leaves a narrow sperm-to-seminal plasma ratio owing to marginal antioxidant support; moreover, semen extension further dilutes the antioxidant level, leading to an imbalance of oxidant-antioxidant equilibrium. The present study aimed to evaluate the effect of quercetin on curtailing oxidative stress and its reflection on the post-thaw survivability and membrane integrity of goat spermatozoa. For this study, six bucks were selected. Six ejaculates from each buck totaling 36 ejaculates were collected, which were then split into five parts; furthermore, each part was added with a semen extender having a particular concentration of additive. Group C without quercetin and T containing Vitamin E at 3 mmol/mL were considered the control and positive control respectively, whereas T, T, and T contain 10, 20, and 30 μmol/mL of Quercetin respectively. The final sperm concentration of each group was kept at 200 × 10 spermatozoa/mL. All groups were subjected to equilibration at 4 °C for 4 h, then filled in French mini (0.25 mL) straws, followed by sealing and cryopreservation. Samples after 72 h of cryopreservation were subjected to evaluation of plasma membrane integrity and viability through staining, acrosomal integrity, and mitochondrial membrane activity through flow cytometry. Evaluation of sperm kinematics as well as the oxidant-antioxidant status of sperm (ROS and nitric oxide) and seminal plasma (SOD, CAT, GPx, FRAP, and lipid peroxidation through MDA estimation) were also carried out. Quercetin, when supplemented at 20 μmol/mL in buck semen extender, significantly (p < 0.01) improved cryopreserved sperm functions in terms of plasma membrane integrity, viability, acrosomal integrity, mitochondrial membrane activity, and sperm kinematics of buck semen. Similarly, Quercetin supplementation at 20 μmol/mL significantly reduced reactive oxygen and nitrogen species (RONS) in sperm and improved the antioxidant status of seminal plasma, which was indicated by reduced oxidative damage and improved the antioxidant status of buck semen. In conclusion, Quercetin at 20 μmol/mL reduced oxidative stress, improved semen antioxidant status, and improved sperm membranes integrity and kinematics.
山羊精子的冷冻保存具有挑战性,这是由于几个因素造成的,其中最重要的因素之一是氧化应激。由于山羊精液的射精量少、精子浓度高,因此氧化应激尤其重要。这使得由于边缘抗氧化支持而导致精子与精浆的比例狭窄;此外,精液的扩展进一步稀释了抗氧化剂的水平,导致氧化剂-抗氧化剂平衡的失衡。本研究旨在评估槲皮素对减少氧化应激的影响及其对山羊精子解冻后存活率和膜完整性的影响。为此,选择了 6 只公山羊。每只公山羊采集 6 份精液,总共采集了 36 份精液,然后将其分为 5 份;此外,每份精液都添加了一种含有特定添加剂浓度的精液稀释液。不含槲皮素的 C 组和含有 3mmol/mL 维生素 E 的 T 组分别作为对照组和阳性对照组,而 T、T 和 T 组分别含有 10、20 和 30μmol/mL 的槲皮素。每组的最终精子浓度均保持在 200×10 个精子/mL。所有组都在 4°C 下平衡 4 小时,然后填充在法国迷你(0.25mL)吸管中,然后密封和冷冻保存。冷冻保存 72 小时后,通过染色评估精子质膜完整性和活力,通过流式细胞术评估顶体完整性和线粒体膜活性。还评估了精子运动学以及精子(ROS 和一氧化氮)和精浆(SOD、CAT、GPx、FRAP 和通过 MDA 估计的脂质过氧化)的氧化还原状态。当在公山羊精液稀释液中补充 20μmol/mL 的槲皮素时,在质膜完整性、活力、顶体完整性、线粒体膜活性和公山羊精液的运动学方面,冷冻保存的精子功能显著提高(p<0.01)。同样,当在公山羊精液稀释液中补充 20μmol/mL 的槲皮素时,精子中的活性氧和氮物种(RONS)显著减少,并改善了精浆的抗氧化状态,这表明氧化损伤减少,公山羊精液的抗氧化状态得到改善。总之,20μmol/mL 的槲皮素减少了氧化应激,改善了精液的抗氧化状态,提高了精子膜的完整性和运动学。