Detecting Neurodevelopmental Effects of Early-Gestation Ethanol Exposure: A Nonhuman Primate Model of Ethanol Drinking During Pregnancy.

IF 3.2 3区 医学 Q1 Medicine
Alcoholism, clinical and experimental research Pub Date : 2019-02-01 Epub Date: 2019-01-11 DOI:10.1111/acer.13938
Vanessa A Jimenez, Xiaojie Wang, Natali Newman, Nicole A R Walter, Steven Gonzales, Jamie O Lo, Mathew M Ford, Verginia C Cuzon Carlson, Kathleen A Grant, Christopher D Kroenke
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引用次数: 6

Abstract

Background: Gestational ethanol (EtOH) exposure is associated with multiple developmental abnormalities, collectively termed fetal alcohol spectrum disorder (FASD). While the majority of women abstain from EtOH following knowledge of pregnancy, one contributing factor to the high FASD prevalence is that pregnancy is not detected until 4 to 6 weeks. Thus, EtOH consumption continues during the initial stages of fetal development.

Methods: An experimental protocol is described in which rhesus macaques self-administer 1.5 g/kg/d EtOH (or isocaloric maltose dextrin) prior to pregnancy and through the first 60 days of a 168-day gestation term. Menstrual cycles were monitored, including measurements of circulating estradiol and progesterone levels. The latency to consume 1.5 g/kg EtOH and blood EtOH concentration (BEC) was measured.

Results: Twenty-eight fetuses (14 EtOH and 14 controls) were generated in this study. EtOH did not affect menstrual cycles or the probability of successful breeding. No EtOH-induced gross adverse effects on pregnancy were observed. Individual variability in latency to complete drinking translated into variability in BEC, measured 90 minutes following session start. Drinking latencies in controls and EtOH drinkers were longer in the second gestational month than in the first. All pregnancies reached the planned experimental time point of G85, G110, or G135, when in utero MRIs were performed, fetuses were delivered by caesarean section, and brains were evaluated with ex vivo procedures, including slice electrophysiology. Fetal tissues have been deposited to the Monkey Alcohol Tissue Research Resource.

Conclusions: This FASD model takes advantage of the similarities between humans and rhesus macaques in gestational length relative to brain development, as well as similarities in EtOH self-administration and metabolism. The daily 1.5 g/kg dose of EtOH through the first trimester does not influence pregnancy success rates. However, pregnancy influences drinking behavior during the second month of pregnancy. Future publications using this model will describe the effect of early-gestation EtOH exposure on anatomical and functional brain development at subsequent gestational ages.

Abstract Image

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检测妊娠早期乙醇暴露对神经发育的影响:怀孕期间饮酒的非人类灵长类动物模型。
背景:妊娠期乙醇(EtOH)暴露与多种发育异常有关,统称为胎儿酒精谱系障碍(FASD)。虽然大多数妇女在知道怀孕后都避免使用EtOH,但导致FASD高患病率的一个因素是直到4至6周才发现怀孕。因此,EtOH消耗在胎儿发育的初始阶段继续。方法:一项实验方案描述了恒河猴自我管理1.5 g/kg/d EtOH(或等热量麦芽糖糊精)在怀孕前和通过前60天的168天妊娠期。监测月经周期,包括测量循环雌二醇和黄体酮水平。测定消耗1.5 g/kg EtOH的潜伏期和血EtOH浓度(BEC)。结果:本研究共产生28例胎儿(EtOH 14例,对照组14例)。EtOH不影响月经周期或成功繁殖的概率。未观察到etoh对妊娠的不良影响。个体完全饮酒延迟的差异转化为BEC的差异,在会话开始后90分钟测量。对照组和EtOH饮酒者在妊娠第二个月的饮酒潜伏期比妊娠第一个月长。所有妊娠均达到计划的实验时间点G85、G110或G135,此时进行宫内核磁共振,剖腹产分娩胎儿,并通过体外程序(包括切片电生理)评估大脑。胎儿组织已存入猴酒精组织研究资源。结论:该FASD模型利用了人类和恒河猴在相对于大脑发育的妊娠期长短以及EtOH自我给药和代谢方面的相似性。妊娠早期每日1.5 g/kg剂量的EtOH不影响妊娠成功率。然而,怀孕会影响怀孕第二个月的饮酒行为。使用该模型的未来出版物将描述妊娠早期暴露于EtOH对随后胎龄大脑解剖和功能发育的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.90
自引率
9.40%
发文量
219
审稿时长
1 months
期刊介绍: Alcoholism: Clinical and Experimental Research''s scope spans animal and human clinical research, epidemiological, experimental, policy, and historical research relating to any aspect of alcohol abuse, dependence, or alcoholism. This journal uses a multi-disciplinary approach in its scope of alcoholism, its causes, clinical and animal effect, consequences, patterns, treatments and recovery, predictors and prevention.
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