da Costa Charles S, Marques Vinícius Bermond, Mageski Jandinay, Santos Paulo Caleb J L, Faria Rodrigo Alves, Sarmento Isabela V, de Oliveira Poliana Borges, Krause Maira, D Carneiro Maria Tereza W, Dos Santos Leonardo, Graceli Jones B
Institute of Biomedical Sciences, Federal University of Rio de Janeiro, 290440-090, Rio de Janeiro, RJ, Brazil; Department of Morphological Sciences, University of Espirito Santo, 290440-090, Vitória, ES, Brazil.
Department of Physiological Sciences, University of Espirito Santo, 290440-090, Vitória, ES, Brazil.
Reprod Toxicol. 2025 Aug 13:109031. doi: 10.1016/j.reprotox.2025.109031.
Iron overload is associated with reproductive abnormalities. For example, a case study showed that despite the iron status normalization following phlebotomies and chelation therapy, a woman with juvenile hemochromatosis (JH) continued to exhibit persistent atrophic ovaries, accompanied by prolonged amenorrhea by clinical evaluations. However, the iron overload consequences in the female hypothalamic-pituitary-gonadal (HPG) axis are incompletely understood. Based on the case-report follow-up of a woman diagnosed with JH, this study elucidated the effects of chronic iron overload on the female mouse model, with a special focus on iron-induced consequences in the HPG axis. Female mice were injected with iron (10mg/mouse/day) five times per week for four weeks, and iron deposits and the reproductive tissues morphology, hormone levels, reactive oxygen species (ROS), and fertility were assessed. Iron-overloaded mice had increased iron levels in serum, hypothalamus, pituitary, ovary, and uterus. Iron-overloaded mice displayed irregular estrous cycles, abnormal folliculogenesis and estrogen levels, reduced corpora lutea and increased atretic follicle numbers. Furthermore, iron overload induced uterine atrophy, along with uterine and ovarian fibrosis. Further iron-overloaded mice increased ROS in the pituitary, ovary and uterus. Positive correlations were found between serum iron levels and ovarian atretic follicles and collagen deposition, and between uterine iron levels and uterine ROS and collagen deposition. In the fertility evaluation, no pups or litters were observed over 90 days in the iron-overloaded mice, suggesting that iron overload causes infertility. Collectively, these findings indicate that chronic iron overload leads to HPG axis abnormalities due to iron accumulation and ROS generation.
铁过载与生殖异常有关。例如,一项病例研究表明,尽管通过放血和螯合疗法使铁状态恢复正常,但一名患有青少年血色病(JH)的女性仍持续表现出卵巢萎缩,并经临床评估伴有长期闭经。然而,铁过载对女性下丘脑 - 垂体 - 性腺(HPG)轴的影响尚未完全明确。基于对一名诊断为JH的女性的病例报告随访,本研究阐明了慢性铁过载对雌性小鼠模型的影响,特别关注铁在HPG轴上引起的后果。每周给雌性小鼠注射铁(10mg/只/天),共注射五次,持续四周,然后评估铁沉积、生殖组织形态、激素水平、活性氧(ROS)和生育能力。铁过载小鼠的血清、下丘脑、垂体、卵巢和子宫中的铁水平升高。铁过载小鼠表现出不规律的发情周期、异常的卵泡发生和雌激素水平、黄体减少以及闭锁卵泡数量增加。此外,铁过载导致子宫萎缩,以及子宫和卵巢纤维化。进一步研究发现,铁过载小鼠的垂体、卵巢和子宫中的ROS增加。血清铁水平与卵巢闭锁卵泡及胶原沉积之间,以及子宫铁水平与子宫ROS及胶原沉积之间存在正相关。在生育能力评估中,铁过载小鼠在90天内未观察到幼崽或窝仔,这表明铁过载会导致不孕。总体而言,这些发现表明慢性铁过载由于铁积累和ROS生成导致HPG轴异常。