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蛋白质缺乏饮食对小鼠无机砷发育毒性的影响。

Effects of protein deficient diets on the developmental toxicity of inorganic arsenic in mice.

作者信息

Lammon Carol A, Hood Ronald D

机构信息

Capstone College of Nursing, The University of Alabama, Tuscaloosa, Alabama, USA.

出版信息

Birth Defects Res B Dev Reprod Toxicol. 2004 Jun;71(3):124-34. doi: 10.1002/bdrb.20006.

Abstract

BACKGROUND

Inorganic arsenic, when given by injection to pregnant laboratory animals (mice, rats, hamsters), has been shown to induce malformations. Arsenic methylation may be a detoxification step, and diets deficient in protein are a poor source of methyl donors and may possibly result in impaired arsenic methylation. Human health effects from chronic arsenic exposure have been reported mainly in populations with low socioeconomic status. Individuals in such populations are likely to suffer from malnutrition, which can compromise embryonic/fetal development and diminish arsenic methylating capacity. We sought to determine if dietary protein deficiency affects the developmental toxicity of inorganic arsenic.

METHODS

Mated females were randomly assigned to one of 12 treatment groups. Experimental groups received either AsIII or AsV i.p. on Gestation Day 8 (GD 8, plug=GD 0) and were maintained on a 5%, 10%, or 20% protein custom mixed diet from GD 1 until sacrifice. Controls received the custom diets alone, were given AsIII or AsV i.p. on GD 8 with Teklad LM-485 rodent diet, or were fed the LM-485 diet alone. Test females were sacrificed on GD 17, and their litters were examined for mortality and developmental defects.

RESULTS

Arsenic plus dietary protein deficiency decreased maternal weight gain and increased the incidences of exencephaly, ablepharia, and skeletal defects, such as malformed vertebral centra, fused ribs, and abnormal sternebrae (bipartite, rudimentary, or unossified).

CONCLUSIONS

These results demonstrate that dietary protein deficiency enhances the developmental toxicity of inorganic arsenic, possibly by impairment of arsenic methylation.

摘要

背景

已证实,给怀孕的实验动物(小鼠、大鼠、仓鼠)注射无机砷会导致畸形。砷甲基化可能是一个解毒步骤,而蛋白质缺乏的饮食是甲基供体的不良来源,可能会导致砷甲基化受损。慢性砷暴露对人类健康的影响主要在社会经济地位较低的人群中被报道。这类人群中的个体可能营养不良,这会损害胚胎/胎儿发育并降低砷甲基化能力。我们试图确定饮食蛋白质缺乏是否会影响无机砷的发育毒性。

方法

将交配后的雌性动物随机分配到12个处理组之一。实验组在妊娠第8天(GD 8,受孕日=GD 0)腹腔注射亚砷酸盐(AsIII)或砷酸盐(AsV),并从GD 1开始维持在含5%、10%或20%蛋白质的定制混合饮食中,直至处死。对照组仅接受定制饮食,在GD 8腹腔注射AsIII或AsV并给予Teklad LM - 485啮齿动物饲料,或仅喂食LM - 485饲料。在GD 17处死受试雌性动物,并检查其窝仔的死亡率和发育缺陷。

结果

砷与饮食蛋白质缺乏共同作用会降低母体体重增加,并增加无脑畸形、无眼畸形和骨骼缺陷的发生率,如椎体畸形、肋骨融合和胸骨异常(二分、发育不全或未骨化)。

结论

这些结果表明,饮食蛋白质缺乏可能通过损害砷甲基化增强无机砷的发育毒性。

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