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饮用水中的亚砷酸盐会使怀孕大鼠及其雌性后代出现葡萄糖耐受不良。

Arsenite in drinking water produces glucose intolerance in pregnant rats and their female offspring.

作者信息

Bonaventura María Marta, Bourguignon Nadia Soledad, Bizzozzero Marianne, Rodriguez Diego, Ventura Clara, Cocca Claudia, Libertun Carlos, Lux-Lantos Victoria Adela

机构信息

Instituto de Biología y Medicina Experimental (IBYME-CONICET), Vuelta de Obligado 2490, C1428ADN, CABA, Argentina; Escuela de Ciencia y Técnica, Universidad Nacional de San Martín, Av 25 de mayo 1650, Partido de San Martín, Bs As, Argentina.

Instituto de Biología y Medicina Experimental (IBYME-CONICET), Vuelta de Obligado 2490, C1428ADN, CABA, Argentina.

出版信息

Food Chem Toxicol. 2017 Feb;100:207-216. doi: 10.1016/j.fct.2016.12.025. Epub 2016 Dec 23.

Abstract

Drinking water is the main source of arsenic exposure. Chronic exposure has been associated with metabolic disorders. Here we studied the effects of arsenic on glucose metabolism, in pregnant and post-partum of dams and their offspring. We administered 5 (A5) or 50 (A50) mg/L of sodium arsenite in drinking water to rats from gestational day 1 (GD1) until two months postpartum (2MPP), and to their offspring from weaning until 8 weeks old. Liver arsenic dose-dependently increased in arsenite-treated rats to levels similar to exposed population. Pregnant A50 rats gained less weight than controls and recovered normal weight at 2MPP. Arsenite-treated pregnant animals showed glucose intolerance on GD16-17, with impaired insulin secretion but normal insulin sensitivity; they showed dose-dependent increased pancreas insulin on GD18. All alterations reverted at 2MPP. Offspring from A50-treated mothers showed lower body weight at birth, 4 and 8 weeks of age, and glucose intolerance in adult females, probably due to insulin secretion and sensitivity alterations. Arsenic alters glucose homeostasis during pregnancy by altering beta-cell function, increasing risk of developing gestational diabetes. In pups, it induces low body weight from birth to 8 weeks of age, and glucose intolerance in females, demonstrating a sex specific response.

摘要

饮用水是砷暴露的主要来源。长期暴露与代谢紊乱有关。在此,我们研究了砷对母鼠及其后代孕期和产后葡萄糖代谢的影响。从妊娠第1天(GD1)至产后两个月(2MPP),我们给大鼠饮用含5(A5)或50(A50)mg/L亚砷酸钠的水,并给其后代从断奶至8周龄饮用该水。在亚砷酸钠处理的大鼠中,肝脏砷含量呈剂量依赖性增加,达到与暴露人群相似的水平。A50组怀孕大鼠体重增加少于对照组,并在2MPP时恢复正常体重。亚砷酸钠处理的怀孕动物在GD16 - 17时出现葡萄糖不耐受,胰岛素分泌受损但胰岛素敏感性正常;在GD18时,它们的胰腺胰岛素呈剂量依赖性增加。所有改变在2MPP时恢复。A50组处理的母鼠后代在出生时、4周和8周龄时体重较低,成年雌性出现葡萄糖不耐受,这可能是由于胰岛素分泌和敏感性改变所致。砷通过改变β细胞功能改变孕期葡萄糖稳态,增加患妊娠期糖尿病的风险。在幼崽中,它导致从出生到8周龄体重偏低,雌性出现葡萄糖不耐受,表明存在性别特异性反应。

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