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硒对氟致雄性大鼠生殖损害的拮抗作用

Experimental study on the antagonism of selenium on male reproductive toxicity of excessive fluorine
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摘要 目的 :探讨硒对高氟所致雄性大鼠生殖损害的拮抗作用。方法 :1 0 0只雄性Wistar大鼠随机分成对照组、氟 (NaF 1 5 0mg/L)组、氟加低硒 (0 .5mg/L亚硒酸钠 )组、氟 (NaF 1 5 0mg/L)加中硒 (2 .0mg/L亚硒酸钠 )组、氟(NaF 1 5 0mg/L)加高硒 (4 .0mg/L亚硒酸钠 )组 5组 ,通过饮水加氟、加硒的方法染毒 1 0周。观察氟、硒对大鼠体重、睾丸和附睾质量及其脏器系数 ,精子计数、活动率及畸形率 ,睾丸、附睾生化标志酶 ,血清性激素 ,睾丸组织病理切片以及初级精母细胞染色体畸形率的影响。结果 :①右侧睾丸质量对照组为 (1 .80± 0 .2 2 )g ,氟加高硒组为 (1 .6 1±0 .1 1 )g ,2者相比差异有统计学意义 (P <0 .0 5 )。②精子计数 :氟组 (9.2 3× 1 0 7ml-1 )、氟加中硒组 (37.6 7× 1 0 7ml-1 )与对照组 (2 8.6 0× 1 0 7ml-1 )比较 ,差异有统计学意义 (P <0 .0 0 1 ) ;精子畸形率 :氟组 (36 .33% )氟加中硒组 (1 2 .70 % )与对照组 (1 4 .83% )比较 ,差异有统计学意义 (P <0 .0 0 1 ) ;精子活动率 :氟组 (6 2 .0 7%± 6 .5 0 % )氟加中硒组 (6 8.2 1 %± 4 .99% )与对照组 (73.6 7%± 6 .5 1 % )比较 ,差异有统计学意义 (P <0 .0 0 1 )。③LDH :氟组 ((5 79.4 7± 97.1 6 )u/g)、氟加中硒组 ((72 6 .1 3± 1 Aim: To study the antagonism of selenium on male reproductive toxicity induced by excessive fluorine. Methods:A total of 100 male Wistar rats were randomly allocated into five groups: control group, fluorine group, fluorine plus low-dose selenium, fluorine plus mid-dose selenium and fluorine with high-dose selenium, then the animals were fed deionized water supplemented with NaF or/and Na 2SeO 3 for ten weeks. The body weights, right testical, right epididymitis and its organic coefficient were measured and calculated; the count of sperm and the rates of sperm mobility and aberration were analyzed; the levels of lactate dehydrogenase(LDH),Na +K +-ATPase, Mg 2+ -ATPase, Ca 2+ -ATPase and serum testosterone(T), luteinizing hormone(LH) were examined; meanwhile the pathological alterations of testes and the chromosome aberration of primary spermatocytes were observed. Result: Weight of right testical was significantly reduced ( P <0.05) in group of fluorine plus high-dose selenium (1.61±0.11)g compared to control (1.80±0.22)g. Sperm count in fluorine group (9.23×10 7 ml -1 ) and fluorine plus mid-dose selenium group (37.67×10 7 ml -1 ) compared to control (28.60×10 7 ml -1 ) had significant differences; significant differences ( P <0.001) were also observed in fluorine group (36.33%) and fluorine plus mid-dose selenium group (12.70%) compared to control rats (14.83%) in the aberration rate of sperm; meanwhile significant differences ( P <0.001) were observed between fluorine group (62.07%±6.50%) and fluorine plus mid-dose selenium group (68.21%±4.99%) compared to control group (73.67%±6.51%) in the rate of sperm mobility. The level of LDH was significantly ( P <0.001) decreased in fluorine (579.47±97.16)u/g and fluorine plus mid-dose selenium (726.13±115.55)u/g compared to control (736.80±86.03)u/g; similar significant ( P < 0.001) changes were found in the level of Na +K +-ATPase in the three groups ((1.04±0.18) μmol·mg -1 ·h -1 , (1.28±0.12) μmol·mg -1 ·h -1 , (1.37±0.21) μmol·mg -1 ·h -1 ); while the level of Mg 2+ -ATPase in the four groups administered fluorine or/and selenium had significant ( P <0.001) differences from that of control. Significant differences ( P <0.05) were observed in fluorine plus mid-dose selenium group (422.3 ng·L -1 ) and fluorine plus high-dose selenium group (339.0 ng·L -1 ) compared to control (260.7 ng·L -1 ) in the T level in serum; and the LH level was significantly ( P <0.05) changed in the fluorine plus low-, mid-, and high-dose selenium groups compared to control respectively. The microstructure of testis was loosened in fluorine group compared to control rats, while the pathological alterations of testis induced by fluoride were counteracted in the fluorine plus low-, mid-, and high-dose selenium groups compared to fluorine group. No significant difference ( P >0.05) was observed after fluorine and/or selenium treatments in the rate of chromosome aberration of primary spermatocytes compared to control group.Conclusions: Fluoride can result in reproductive toxicity in male rats, and appropriate selenium takin can antagonize the toxicity of fluoride.
出处 《郑州大学学报(医学版)》 CAS 北大核心 2003年第6期896-900,共5页 Journal of Zhengzhou University(Medical Sciences)
基金 河南省重大科技攻关资助项目 ( 1998-0 6)
关键词 拮抗作用 雄性生殖毒性 fluorine selenium antagonism male reproductive toxicity
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