Transcriptional regulatory dynamics of the hypothalamic-pituitary-testicular axis in male mice exposed to fluoride.
Transcriptional regulatory dynamics of the hypothalamic-pituitary-testicular axis in male mice exposed to fluoride.
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DOI:
10.1016/j.etap.2015.08.007
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发表时间:
2015-09
影响因子:
4.3
通讯作者:
R. Niu;Jianming Wang;Zilong Sun;X. Xue;Xiaoyan Yan;Jinming Wang;Jianhai Zhang;Jundong Wang
中科院分区:
文献类型:
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作者:
R. Niu;Jianming Wang;Zilong Sun;X. Xue;Xiaoyan Yan;Jinming Wang;Jianhai Zhang;Jundong Wang
It is well known that fluoride (F) is a widespread natural pollutant, which naturally exists in soil, water, food, and various kinds of dental care products. US National Research Council points out that at present, millions of people are exposed to high F in their drinking water, especially in China, India, and Mexico (Doull et al., 2006). For example, according to the official data, there are 92 million residents with fluorosis in 28 provinces in China (China News, 2012). In India, 60 million people live in 20 states in endemic areas of fluorosis (Saxena et al., 2012), and more than 6 million inhabitants in risk areas in Mexico (Hurtado and Gardea-Torresdey, 2004). Fluorosis is considered to be a public health issue in world. Besides bone and tooth, non-hard tissues are also the toxic targets of F.The reproductive toxicity of F has been confirmed by epidemiological and laboratory studies, which showed that spermatogenesis (Pushpalatha et al., 2005), sperm morphology and motility (Spittle, 2009), sperm hyperactivation (Sun et al., 2011), sperm fertilizing ability (Dvoráková-Hortová et al., 2008), and reproductive hormones secretion (Ortiz-Pérez et al., 2003, Susheela and Jethanandani, 1996) were adversely affected by high F exposure. Reproductive hormones, including testosterone (T), follicle-stimulating hormone (FSH) and luteinizing hormone (LH), are required for testicular androgenesis and normal spermatogenesis. Zhou et al. found that F ingestion significantly lowered the concentration of FSH, LH, T, progesterone (P), and estradiol (E 2) in female rats (Zhou et al., 2013), which was supported by results from other studies on rats (Ghosh et al., 2002, Sarkar et al., 2006). It is well known that the secretion of these hormones relies on both hypothalamic-pituitary regulation and testicular steroidogenesis. However, which tissues, hormones, and key enzymes in hypothalamic-pituitary-testicular (HPT) axis were associated with the mechanism of F-induced reproductive dysfunction remains largely unknown.