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砷暴露对不同发育阶段子代小鼠海马中 D-丝氨酸代谢的影响。

Effects of arsenic exposure on D-serine metabolism in the hippocampus of offspring mice at different developmental stages.

机构信息

Department of Occupational and Environmental Health, School of Public Health, Shenyang Medical College, No. 146 Huanghe North Street, Yuhong District, Shenyang, 110034, Liaoning, People's Republic of China.

Department of Toxicology, School of Public Health, Shenyang Medical College, Shenyang, Liaoning, People's Republic of China.

出版信息

Arch Toxicol. 2020 Jan;94(1):77-87. doi: 10.1007/s00204-019-02616-1. Epub 2019 Nov 11.

Abstract

The main purpose of this study was to verify the hypothesis that cognitive dysfunctions induced by arsenic exposure were related to the changes of D-serine metabolism in the hippocampus of offspring mice. Mother mice and their offsprings were exposed to 0, 15, 30 or 60 mg/L sodium arsenite (NaAsO) through drinking water from the first day of gestation until the end of lactation. D-serine levels in the hippocampus of mice of postnatal day (PND) 10, 20 and 40 were examined by high-performance liquid chromatography. Expressions of serine racemase (SR), D-amino acid oxidase (DAAO), alanine-serine-cysteine transporter-1 (asc-1) and subunits of N-methyl-D-aspartate receptors (NMDARs) in the hippocampus of mice were measured by Western blot and Real-time RT-PCR. Results showed that arsenic exposure significantly decreased D-serine levels of mice exposed to 60 mg/L NaAsO. Exposure to 60 mg/L NaAsO could inhibit both mRNA and protein expression of SR, whereas increase in the protein expression of DAAO, only enhances the mRNA levels of DAAO of PND 20 mice. In addition, arsenic exposure could upregulate protein expression of asc-1. The mRNA and protein levels of NR1, NR2A and NR2B in the hippocampus of mice were down-regulated by arsenic. Findings from this study suggested that SR might play an important role in the reduction of D-serine levels caused by arsenic exposure, which might further influence the levels of NMDAR subunits especially on PND20, and then might disturb the function of NMDARs and cause the deficits of learning and memory ability of offspring mice.

摘要

本研究的主要目的是验证这样一个假设,即砷暴露引起的认知功能障碍与仔鼠海马中 D-丝氨酸代谢的变化有关。母鼠及其幼仔从受孕第一天开始通过饮用水暴露于 0、15、30 或 60mg/L 亚砷酸钠(NaAsO),直至哺乳期结束。通过高效液相色谱法检测仔鼠出生后第 10、20 和 40 天海马中的 D-丝氨酸水平。通过 Western blot 和 Real-time RT-PCR 检测仔鼠海马中丝氨酸消旋酶(SR)、D-氨基酸氧化酶(DAAO)、丙氨酸-丝氨酸-半胱氨酸转运体-1(asc-1)和 N-甲基-D-天冬氨酸受体(NMDARs)亚基的表达。结果表明,砷暴露显著降低了暴露于 60mg/L NaAsO 的小鼠的 D-丝氨酸水平。暴露于 60mg/L NaAsO 可抑制 SR 的 mRNA 和蛋白表达,而仅增加 PND20 小鼠的 DAAO 蛋白表达,增加 DAAO 的 mRNA 水平。此外,砷暴露可上调 asc-1 的蛋白表达。砷暴露可上调小鼠海马中 NR1、NR2A 和 NR2B 的 mRNA 和蛋白表达。本研究结果表明,SR 可能在砷暴露引起的 D-丝氨酸水平降低中发挥重要作用,这可能进一步影响 NMDAR 亚基的水平,特别是在 PND20 时,从而可能干扰 NMDAR 的功能并导致仔鼠学习和记忆能力的缺陷。

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