a Department of Nutrition , Tianjin Institute of Health and Environmental Medicine , Tianjin 300050 , China.
b Department of Nutrition and Food Hygiene , West China School of Public Health, Sichuan University , Chengdu 610041 , China.
Nutr Neurosci. 2017 Nov;20(9):519-525. doi: 10.1080/1028415X.2016.1194554. Epub 2016 Jun 22.
This study was carried out to understand the effects of zinc deficiency in rats aged 0∼2 months on learning and memory, and the brain-derived neurotrophic factor (BDNF) gene methylation status in the hippocampus.
The lactating mother rats were randomly divided into three groups (n = 12): zinc-adequate group (ZA: zinc 30 mg/kg diet), zinc-deprived group (ZD: zinc 1 mg/kg diet), and a pair-fed group (PF: zinc 30 mg/kg diet), in which the rats were pair-fed to those in the ZD group. After weaning (on day 23), offspring were fed the same diets as their mothers. After 37 days, the zinc concentrations in the plasma and hippocampus were measured, and the behavioral function of the offspring rats was measured using the passive avoidance performance test. We then assessed the DNA methylation patterns of the exon IX of BDNF by methylation-specific quantitative real-time PCR and the mRNA expression of BDNF in the hippocampus by RT-PCR.
Compared with the ZA and PF groups, rats in the ZD group had shorter latency period, lower zinc concentrations in the plasma and hippocampus (P < 0.05). Interestingly, the DNA methylation of the BDNF exon IX was significantly increased in the ZD group, compared with the ZA and PF groups, whereas the expression of the BDNF mRNA was decreased. In addition, the DNMT1 mRNA expression was significantly upregulated and DNMT3A was downregulated in the ZD group, but not in the ZA and PF groups.
The learning and memory damage in offspring may be a result of the epigenetic changes of the BDNF genes in response to the zinc-deficient diet during 0∼2 month period. Furthermore, this work supports the speculative notion that altered DNA methylation of BDNF in the hippocampus is one of the main causes of cognitive impairment by zinc deficiency.
本研究旨在探讨 0~2 月龄缺锌对大鼠学习记忆能力的影响及其海马脑源性神经营养因子(BDNF)基因甲基化状态。
哺乳期母鼠随机分为 3 组(n=12):锌充足组(ZA:锌 30mg/kg 饮食)、缺锌组(ZD:锌 1mg/kg 饮食)和等热量喂养组(PF:锌 30mg/kg 饮食),后者与 ZD 组等热量喂养。断乳后(第 23 天),仔鼠给予与其母鼠相同的饮食。37 天后,检测仔鼠血浆和海马锌浓度,利用被动回避性能测试检测仔鼠行为功能。采用甲基化特异性定量实时 PCR 检测 BDNF 外显子 IX 的 DNA 甲基化模式,RT-PCR 检测海马 BDNF mRNA 表达。
与 ZA 和 PF 组相比,ZD 组仔鼠潜伏期缩短,血浆和海马锌浓度降低(P<0.05)。有趣的是,ZD 组 BDNF 外显子 IX 的 DNA 甲基化显著增加,而 BDNF mRNA 的表达减少。此外,ZD 组 DNMT1mRNA 表达明显上调,DNMT3A 下调,但 ZA 和 PF 组未见此变化。
0~2 月龄缺锌导致仔鼠学习记忆损伤可能是由于缺锌饮食导致 BDNF 基因表观遗传改变所致。此外,本研究支持锌缺乏导致认知障碍的主要原因之一是海马 BDNF 基因的 DNA 甲基化改变的推测。