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短链氯化石蜡可能通过AIM2和NLRP12炎性小体诱导小鼠卵巢损伤。

Short-Chain Chlorinated Paraffins May Induce Ovarian Damage in Mice via AIM2- and NLRP12-PANoptosome.

作者信息

Bai Mingxin, Lei Jiawei, Li Fan, Wang Xuning, Fu Hu, Yan Zhengli, Zhu Yongfei

机构信息

Key Laboratory of Study and Discovery of Small Targeted Molecules of Hunan Province, Department of Preventive Medicine, Medical school, Hunan Normal University, Changsha, Hunan 410013, China.

Key Laboratory of Protein Chemistry and Fish Developmental Biology of Ministry of Education, Hunan Normal University, Changsha, 410081, China.

出版信息

Environ Sci Technol. 2025 Jan 14;59(1):163-176. doi: 10.1021/acs.est.4c08622. Epub 2025 Jan 4.

Abstract

Humans may intake 0.02 mg/kg/day of short-chain chlorinated paraffins (SCCPs), and no study is available on mammalian ovarian damage caused by low-level SCCPs. In this study, four groups of 5-week-old female Institute of Cancer Research (ICR) mice were orally administered 0, 0.01, 0.1, and 1.0 mg/kg/day SCCPs for 21 consecutive days, and serum and ovaries were collected 20 h after the last SCCPs-administration. SCCPs at ≥0.1 mg/kg/day were found to reduce follicle counts at each stage, induce dose-dependent oxidative stress in mice, and lower serum E2 and ovarian anti-Müllerian hormone levels. The data indicated that cellular PANoptosis increased in the ovaries of all SCCP-treated mice. Furthermore, AIM2- and NLRP12-PANoptosome gene and protein levels were considerably elevated. Female germline stem cells (FGSCs) in the cortical portion of the ovary exhibited substantial damage in all SCCP groups, additionally, the expression of FGSC marker genes and major marker proteins was diminished in the ovaries. Oral administration of SCCPs with 0.01, 0.1, and 1.0 mg/kg/day to mice resulted in PANoptosis of the ovaries. Therefore, it was suggested that the oral administration of ≥0.1 mg/kg/day of SCCPs suppressed ovarian function, which may be attributed to the fact that SCCPs induced the generation of AIM2- and NLRP12-PANoptosome in ovary cells.

摘要

人类每天可摄入0.02毫克/千克的短链氯化石蜡(SCCPs),目前尚无关于低水平SCCPs对哺乳动物卵巢损伤的研究。在本研究中,将四组5周龄的雌性癌症研究所(ICR)小鼠连续21天每天口服给予0、0.01、0.1和1.0毫克/千克的SCCPs,并在最后一次给予SCCPs后20小时收集血清和卵巢。发现每天给予≥0.1毫克/千克的SCCPs会减少各阶段的卵泡数量,在小鼠中诱导剂量依赖性氧化应激,并降低血清E2和卵巢抗苗勒管激素水平。数据表明,所有接受SCCP处理的小鼠卵巢中的细胞全凋亡增加。此外,AIM2和NLRP12全凋亡小体基因及蛋白水平显著升高。卵巢皮质部分的雌性生殖干细胞(FGSCs)在所有SCCP组中均表现出严重损伤,此外,卵巢中FGSC标记基因和主要标记蛋白的表达减少。给小鼠每天口服0.01、0.1和1.0毫克/千克的SCCPs会导致卵巢全凋亡。因此,提示每天口服≥0.1毫克/千克的SCCPs会抑制卵巢功能,这可能归因于SCCPs诱导卵巢细胞中AIM2和NLRP12全凋亡小体的产生。

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