脱氧雪腐镰刀菌醇诱导围青春期大鼠卵巢凋亡

J. Gerez, Gisele Augusta Amorim de Lemos, Thaynara Camacho, V. H. Marutani, L. Chuffa, Henrique Spaulonci Silveira, W. A. Verri, Eduardo Micotti da Gloria, Ana Paula Frederico Rodrigues Loureiro Bracarence
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摘要

青春期受内分泌系统支配,通过一系列生理和生物转化,标志着动物和人类生殖功能的开始。尽管霉菌毒素 DON 可破坏荷尔蒙平衡并导致生殖异常,但其对青春期相关生殖变化的影响仍未得到充分研究。考虑到儿童和青少年接触 DON 的机会增多,我们的研究旨在阐明 DON 对幼鼠卵巢组织中卵泡完整性以及促凋亡蛋白(BAX 和 Caspase-3)和抗凋亡蛋白(BCL-2)表达的影响。我们将 10 只 28 天大的青春期前 Wistar 大鼠分为两个饮食组,每组 28 天:对照组饮食不含霉菌毒素,DON 组饮食含 10 毫克 DON/Kg。实验结束后,记录卵巢和子宫的重量,并对卵巢进行形态计量和免疫组化分析。暴露于 DON 会导致卵巢和子宫重量明显下降。虽然摄入 DON 不会改变各发育阶段卵巢卵泡的数量,但我们观察到在大多数卵泡阶段和黄体中,BAX 和 Caspase-3 的表达增加,BCL-2 的表达减少。总之,在青春期接触 DON 会干扰成年早期不同卵巢细胞群的凋亡过程。
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Deoxynivalenol induces ovarian apoptosis in peripubertal rats
Puberty, governed by the endocrine system, marks the onset of reproductive functions in animals and humans through a series of physiological and biological transformations. Although the mycotoxin DON can disrupt hormonal balance and cause reproductive abnormalities, its impact on puberty-associated reproductive changes remains understudied. Considering the increased exposure of children and adolescents to DON, our study aimed to elucidate its influence on follicular integrity and the expression of pro-apoptotic proteins (BAX and Caspase-3) and anti-apoptotic protein (BCL-2) in juvenile rat ovarian tissue. We divided ten 28-day-old prepubertal Wistar rats into two dietary groups for 28 days: a control group with a mycotoxin-free diet and a DON group with a diet containing 10 mg DON/Kg. After the experiment, ovaries and uterus weights were recorded, and the ovaries underwent morphometric and immunohistochemical analysis. DON exposure led to significant reductions in both ovarian and uterine weights. Although DON intake did not change the number of ovarian follicles across developmental stages, we observed an increased expression of BAX and Caspase-3 and a decreased BCL-2 expression in most follicular stages and corpora lutea. In summary, DON exposure during puberty can interfere with apoptotic processes in diverse ovarian cell populations during early adulthood.
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