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氟化物钠对小鼠精子超活化及钙离子信号通路的影响:一项体内研究。

Effects of sodium fluoride on hyperactivation and Ca2+ signaling pathway in sperm from mice: an in vivo study.

机构信息

Shanxi Key Laboratory of Ecological Animal Science and Environmental Medicine, Shanxi Agricultural University, Taigu, 030801 Shanxi, People's Republic of China.

出版信息

Arch Toxicol. 2010 May;84(5):353-61. doi: 10.1007/s00204-009-0508-x. Epub 2010 Jan 6.

Abstract

Sperm hyperactivation is crucial for a successful fertilization; however, the influence of fluoride (F) to hyperactivation is still in its infancy. The purpose of this study was to investigate the effect of sodium fluoride (NaF) on sperm hyperactivation, Ca2+/CALM-CAMK2 signaling, and CatSper1 and CatSper2 mRNA expression in mice sperm. Adult male Kunming mice were administrated with 30, 70, and 150 mg NaF/l (corresponding to 2.84 +/- 0.29, 6.28 +/- 0.61, and 14.18 +/- 1.00 mg F/kg body weight per day) through drinking water for 49 days. The results showed that NaF reduced the sperm hyperactivated motility in a dose-dependent manner. Compared with the controls, intracellular Ca2+ concentration and CAMK2 protein were significantly decreased in mice treated with 70 and 150 mg NaF/l, while no effect on CALM was determined in all treatment groups. Furthermore, decreased sperm CatSper1 mRNA expression was also observed in response to middle and higher doses of NaF (70, 150 mg/l) with comparison to the control group, whereas no change in the mRNA expression of CatSper2 was detected in NaF administrated groups. Treatment with 30 mg NaF/l exhibited slight effects on the above indexes with no statistical difference. These findings indicated that exposure to 70 and 150 mg/l NaF for 49 days could result in low hyperactivation via alteration of Ca2+ signaling pathway involving CatSper1 in sperm from mice.

摘要

精子超激活对于成功受精至关重要;然而,氟化物(F)对超激活的影响仍处于初级阶段。本研究旨在探讨氟化钠(NaF)对小鼠精子超激活、Ca2+/CALM-CAMK2 信号转导以及 CatSper1 和 CatSper2 mRNA 表达的影响。成年雄性昆明小鼠通过饮用含 30、70 和 150 mg NaF/L(分别相当于每天 2.84 +/- 0.29、6.28 +/- 0.61 和 14.18 +/- 1.00 mg F/kg 体重)的水,连续 49 天。结果表明,NaF 呈剂量依赖性降低精子超激活运动。与对照组相比,70 和 150 mg NaF/L 处理组的细胞内 Ca2+浓度和 CAMK2 蛋白显著降低,而所有处理组的 CALM 均无影响。此外,还观察到中高剂量 NaF(70、150 mg/L)处理组的精子 CatSper1 mRNA 表达降低,而 NaF 处理组的 CatSper2 mRNA 表达无变化。30 mg NaF/L 处理组对上述指标仅有轻微影响,无统计学差异。这些发现表明,暴露于 70 和 150 mg/L NaF 49 天可导致小鼠精子超激活降低,这可能是通过改变涉及 CatSper1 的 Ca2+信号通路所致。

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