1.5和4.3Ghz单次和联合高功率微波暴露对男性生殖损伤的氧化应激和能量代谢

IF 3.3 4区 医学 Q2 REPRODUCTIVE BIOLOGY Reproductive toxicology Pub Date : 2024-11-29 DOI:10.1016/j.reprotox.2024.108759
Yanyang Li , Binwei Yao , Junqi Men , Yueyue Pang , Jingchao Gao , Yanxin Bai , Hui Wang , Jing Zhang , Li Zhao , Xinping Xu , Ji Dong , Congsheng Li , Ruiyun Peng
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引用次数: 0

摘要

多频电磁环境对男性生殖的影响引起了医学界的关注。单频微波暴露对男性生殖的影响和机制已有研究,但对高功率微波复合辐射和单次微波暴露的比较研究还很少。本研究旨在探讨1.5GHz和4.3GHz微波联合暴露对男性生殖的影响及其机制。雄性Wistar大鼠分别暴露于1.5GHz (l波段)和4.3GHz (c波段)电磁辐射15min。四组分别为:假药组、10mW/cm²l波段组、10mW/cm²c波段组、5mW/cm²l波段和5mW/cm²c波段复合组。评估放疗后睾丸病理结构、精子活力、血清性激素、氧化应激和能量代谢水平。分别暴露在1.5GHz和4.3GHz的微波下会导致睾丸组织损伤和精子质量下降。HPM复合材料与单次暴露的损伤差异不大。暴露组在暴露后第1天和第7天出现组织学和超微结构变化,精子活力、运动参数以及血清睾酮、促黄体生成素、促卵泡激素和血清抑制素- b均下降。这些在第14天有部分恢复的趋势。暴露后睾丸组织中三磷酸腺苷含量降低,乳酸脱氢酶和琥珀酸脱氢酶活性降低,对应于超氧化物歧化酶活性降低,丙二醛含量升高。L-和c -波段HPM的单独和联合暴露都会影响男性生殖系统。暴露于单一和复合HPM的风险无显著差异,氧化应激和能量代谢紊乱起关键作用。
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Oxidative stress and energy metabolism in male reproductive damage from single and combined high-power microwave exposure at 1.5 and 4.3GHz
The effect of multi-frequency electromagnetic environments on male reproduction has attracted the medical community’s interest. Studies have investigated the effects and mechanisms of single-frequency microwave exposure on male reproduction, but comparative research on high-power microwave (HPM) composite and single exposure remains scarce. This study aimed to examine the effects and mechanisms of combined 1.5 GHz and 4.3 GHz microwave exposure on male reproduction. Male Wistar rats were exposed to 1.5 GHz (L-band) and 4.3 GHz (C-band) electromagnetic radiation for 15 minutes. The four groups were: sham, 10 mW/cm² L-band, 10 mW/cm² C-band, and 5 mW/cm² L-band and 5 mW/cm² C-band compound. Assessments were made on the pathological structures of testes, sperm viability, serum sex hormones, oxidative stress, and energy metabolism levels after radiation. Exposure to 1.5 GHz and 4.3 GHz microwaves individually resulted in testicular tissue damage and reduced sperm quality. There was little difference between the damage caused by HPM composite and single exposure. The exposed groups showed histological and ultrastructural changes, with reduced spermatozoa viability, motility parameters, and serum testosterone, luteinizing hormone, follicle-stimulating hormone, and serum inhibin-B on days 1 and 7 after exposure. These tended to recover partially by day 14. Adenosine triphosphate content and lactate dehydrogenase and succinate dehydrogenase activities in the exposed testicular tissue decreased, corresponding to decreased superoxide dismutase activity and increased malondialdehyde content. Both single and combined exposure to L- and C-band HPM affect the male reproductive system. Exposure to single and compound HPM shows no significant difference in risks, with oxidative stress and energy metabolism disturbances playing key roles.
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来源期刊
Reproductive toxicology
Reproductive toxicology 生物-毒理学
CiteScore
6.50
自引率
3.00%
发文量
131
审稿时长
45 days
期刊介绍: Drawing from a large number of disciplines, Reproductive Toxicology publishes timely, original research on the influence of chemical and physical agents on reproduction. Written by and for obstetricians, pediatricians, embryologists, teratologists, geneticists, toxicologists, andrologists, and others interested in detecting potential reproductive hazards, the journal is a forum for communication among researchers and practitioners. Articles focus on the application of in vitro, animal and clinical research to the practice of clinical medicine. All aspects of reproduction are within the scope of Reproductive Toxicology, including the formation and maturation of male and female gametes, sexual function, the events surrounding the fusion of gametes and the development of the fertilized ovum, nourishment and transport of the conceptus within the genital tract, implantation, embryogenesis, intrauterine growth, placentation and placental function, parturition, lactation and neonatal survival. Adverse reproductive effects in males will be considered as significant as adverse effects occurring in females. To provide a balanced presentation of approaches, equal emphasis will be given to clinical and animal or in vitro work. Typical end points that will be studied by contributors include infertility, sexual dysfunction, spontaneous abortion, malformations, abnormal histogenesis, stillbirth, intrauterine growth retardation, prematurity, behavioral abnormalities, and perinatal mortality.
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