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马兜铃酸 I 通过激活 NLRP3 炎性小体和影响线粒体稳态触发卵巢功能障碍。

Aristolochic acid I exposure triggers ovarian dysfunction by activating NLRP3 inflammasome and affecting mitochondrial homeostasis.

机构信息

Medical College, Guangxi University, Nanning, Guangxi, 530004, China.

Translational Medicine Research Center, Ruikang Hospital Affiliated to Guangxi University of Chinese Medicine, Nanning, Guangxi, 530011, China.

出版信息

Free Radic Biol Med. 2023 Aug 1;204:313-324. doi: 10.1016/j.freeradbiomed.2023.05.009. Epub 2023 May 17.

Abstract

Aristolochic acids are widely distributed in the plants of Aristolochiaceae family and Asarum species. Aristolochic acid I (AAI) is the most frequent compound of aristolochic acids, which can accumulate in the soil, and then contaminates crops and water and enters the human body. Research has shown that AAI affects the reproductive system. However, the mechanism of AAI's effects on the ovaries at the tissue level still needs to be clarified. In this research, we found AAI exposure reduced the body and ovarian growth in mice, decreased the ovarian coefficient, prevented follicular development, and increased atretic follicles. Further experiments showed that AAI upregulated nuclear factor-κB and tumor necrosis factor-α expression, activated the NOD-like receptor protein 3 inflammasome, and led to ovarian inflammation and fibrosis. AAI also affected mitochondrial complex function and the balance between mitochondrial fusion and division. Metabolomic results also showed ovarian inflammation and mitochondrial dysfunction due to AAI exposure. These disruptions reduced the oocyte developmental potential by forming abnormal microtubule organizing centers and expressing abnormal BubR1 to destroy spindle assembly. In summary, AAI exposure triggers ovarian inflammation and fibrosis, affecting the oocyte developmental potential.

摘要

马兜铃酸广泛存在于马兜铃科植物和细辛属植物中。马兜铃酸 I(AAI)是马兜铃酸中最常见的化合物,它可以在土壤中积累,然后污染农作物和水,进入人体。研究表明,AAI 会影响生殖系统。然而,AAI 对组织水平卵巢的作用机制仍需阐明。在这项研究中,我们发现 AAI 暴露会减少小鼠的身体和卵巢生长,降低卵巢系数,阻止卵泡发育,并增加闭锁卵泡。进一步的实验表明,AAI 上调了核因子-κB 和肿瘤坏死因子-α 的表达,激活了 NOD 样受体蛋白 3 炎性小体,导致卵巢炎症和纤维化。AAI 还影响线粒体复合物功能和线粒体融合与分裂的平衡。代谢组学结果也表明,AAI 暴露会导致卵巢炎症和线粒体功能障碍。这些破坏通过形成异常的微管组织中心和表达异常的 BubR1 来破坏纺锤体组装,从而降低卵母细胞的发育潜能。总之,AAI 暴露会引发卵巢炎症和纤维化,影响卵母细胞的发育潜能。

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