肥胖小鼠玻璃化解冻卵母细胞解冻后存活和功能完整性的差异。

IF 1.9
Sandhya Kumari, Aparna Chelvi, Vanishree Vasave Madhvacharya, Aishwarya Ashok, Mouna Bannur Karunakara, Yashas Kiran Ninjoor, Jyolsna Ponnaratta Kunhiraman, Amrutha Nedumbrakkad Kunnath, Keerthana Karunakar Poojary, Sneha Guruprasad Kalthur, Satish Kumar Adiga, Guruprasad Kalthur
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引用次数: 0

摘要

目的:已知女性肥胖与卵巢功能受损有关。在这种条件下,卵母细胞的特点是细胞质氧化应激升高,细胞质组织不良,这可能会影响卵母细胞对冻融过程等外源应激的耐受性。本研究探讨了高脂肪饮食(HFD)诱导的肥胖小鼠卵母细胞的低温敏感性。方法:将3周龄雌性小鼠分为正常鼠粮对照组和肥胖鼠粮组,喂养12周。两组卵母细胞均进行玻璃化和解冻处理。评估解冻后存活、活性氧(ROS)水平、线粒体和内质网(ER)分布、内质网应激以及GV期卵母细胞的成熟潜能。结果:尽管肥胖小鼠卵母细胞中脂质积累增加,ROS水平升高,但两组间GV卵母细胞解冻后存活率相当。然而,肥胖引起线粒体和内质网分布的改变。此外,来自肥胖小鼠玻璃化解冻胚泡期(GV)卵母细胞的MII卵母细胞显示出更高的纺锤体缺陷百分比。冻融GV卵母细胞内质网应激标志物GRP78和ATF4较对照组显著升高。结论:这些研究结果表明,母亲肥胖不会显著影响卵母细胞的冷冻存活,但它确实会影响玻璃化后卵母细胞的质量,这强调了在接受抗逆转录病毒治疗的肥胖患者中优化冷冻保存策略的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Disparity between Post-thaw Survival and Functional Integrity of Vitrified-thawed Oocytes from Obese Mice.

Objective: Obesity in women is known to be associated with compromised ovarian function. The oocytes are characterized by elevated cytoplasmic oxidative stress and poor cytoplasmic organization under such conditions, which might affect their tolerance to exogenous stresses such as the freeze-thaw process. This study investigates the cryosusceptibility of oocytes derived from mice with high-fat diet (HFD)-induced obesity.

Methods: Three-weeks-old female mice were divided into a control group (fed a normal chow diet) and an obese group (fed with HFD for 12 weeks). Oocytes from both groups were subjected to vitrification and thawing. Post-thaw survival, reactive oxygen species (ROS) levels, mitochondrial and endoplasmic reticulum (ER) distribution, ER stress, and the maturation potential of GV stage oocytes were evaluated.

Results: Despite increased lipid accumulation and higher ROS levels observed in the oocytes of obese mice, the post-thaw survival rate of GV oocytes was comparable between the groups. However, obesity induced alterations in mitochondrial and ER distribution. Additionally, MII oocytes derived from vitrified-thawed germinal vesicle (GV) stage oocytes of obese mice showed a significantly higher percentage of spindle defects. A notable increase in ER stress markers GRP78 and ATF4 was detected in frozen-thawed GV oocytes compared to the control group.

Conclusions: These findings suggest that maternal obesity does not significantly affect the cryosurvival of oocytes, but it does compromise oocyte quality after vitrification, underscoring the need for optimized cryopreservation strategies in obese patients undergoing ART.

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