Fine particle matter disrupts the blood-testis barrier by activating TGF-β3/p38 MAPK pathway and decreasing testosterone secretion in rat

被引:56
|
作者
Liu, Jianhui [1 ,2 ]
Ren, Lihua [1 ,3 ]
Wei, Jialiu [1 ,2 ]
Zhang, Jin [1 ,2 ]
Zhu, Yupeng [1 ,2 ]
Li, Xiangyang [1 ,2 ]
Jing, Li [1 ,2 ]
Duan, Junchao [1 ,2 ]
Zhou, Xianqing [1 ,2 ]
Sun, Zhiwei [1 ,2 ]
机构
[1] Capital Med Univ, Sch Publ Hlth, Dept Toxicol & Hygien Chem, Beijing 100069, Peoples R China
[2] Capital Med Univ, Beijing Key Lab Environm Toxicol, Beijing 100069, Peoples R China
[3] Peking Univ, Sch Nursing, Beijing 100191, Peoples R China
基金
中国国家自然科学基金;
关键词
androgenic hormones; blood-testis barrier; fine particulate matter; male reproductive toxicity; rat; TGF-beta 3/p38MAPK pathway; NECROSIS-FACTOR-ALPHA; PARTICULATE MATTER; SERTOLI-CELL; SEMINIFEROUS EPITHELIUM; AIR-POLLUTION; IN-VIVO; CARDIOVASCULAR-DISEASE; SIGNALING PATHWAYS; ANDROGEN RECEPTOR; INTERFERON-GAMMA;
D O I
10.1002/tox.22556
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Fine particle matter (PM) is correlated with male reproductive dysfunction in animals and humans, but the underlying mechanisms remain unknown. To investigate the toxic mechanism of PM, 32 male Sprague-Dawley (SD) rats were exposed to saline or PM2.5 with the doses of 1.8, 5.4, and 16.2 mg/kg.b.w. via intratracheal instillation, respectively, one time every 3 days, in total times for 30 days. Sperm concentration, hormone level, the expressions of BTB-associated protein and the mitogen-activated protein kinase (MAPK) pathway, tumor necrosis factor and transforming growth factor 3 levels were detected. The results showed a decrease in sperm number, testosterone and luteinizing hormone levels and altered ultrastructure of BTB in testis of rat after exposure to PM2.5. The protein levels of N-Cadherin, Occludin, Claudin-11, and Connexin-43 were significantly decreased in the testes. TGF-3 content in testes showed increase, with the p-p38/p38 MAPK ratio also increasing after PM2.5 exposure. These results demonstrate that PM2.5 restrained the expressions of BTB-associated proteins through activating TGF-3/p38 MAPK pathway and decreasing testosterone secretion, and therefore lead to the damage of BTB resulting in the decrease of sperm quality, which might be the potential reasons for its negative effects on spermatogenesis and male reproduction.
引用
收藏
页码:711 / 719
页数:9
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