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在大脑发育期间单次接触酒精会在基因易感性小鼠中诱发小头畸形和神经元损失,但在野生型小鼠中则不会。

A single exposure to alcohol during brain development induces microencephaly and neuronal losses in genetically susceptible mice, but not in wild type mice.

作者信息

de Licona Hannah Klein, Karacay Bahri, Mahoney Jo, McDonald Elizabeth, Luang Thirath, Bonthius Daniel J

机构信息

Neuroscience Graduate Program, University of Iowa College of Medicine, Iowa City, IA, United States.

出版信息

Neurotoxicology. 2009 May;30(3):459-70. doi: 10.1016/j.neuro.2009.01.010. Epub 2009 Feb 10.

Abstract

Maternal alcohol abuse during pregnancy can damage the fetal brain and lead to fetal alcohol syndrome (FAS). Despite public warnings discouraging alcohol use during pregnancy, many pregnant women continue to drink intermittently because they do not believe that occasional exposures to alcohol can be harmful to a fetus. However, because of genetic differences, some fetuses are much more susceptible than others to alcohol-induced brain injury. Thus, a relatively low quantity of alcohol that may be innocuous to most fetuses could damage a genetically susceptible fetus. Neuronal nitric oxide synthase (nNOS) can protect developing mouse neurons against alcohol toxicity by synthesizing neuroprotective nitric oxide. This study examined whether a single exposure to alcohol, which causes no evident injury in wild type mice, can damage the brains of mice genetically deficient for nNOS (nNOS-/- mice). Wild type and nNOS-/- mice received intraperitoneal injections of alcohol (0.0, 2.2, or 4.4mg/g body weight) either as a single dose on postnatal day (PD) 4 or as repeated daily doses over PD4-9. Brain volumes and neuronal numbers within the hippocampus and cerebral cortex were determined on PD10. Alcohol exposure on PD4-9 restricted brain growth and caused neuronal death in both strains of mice, but the severity of microencephaly and neuronal loss were more severe in the nNOS-/- mice than in wild type. The 4.4 mg/g alcohol dose administered on PD4 alone caused significant neuronal loss and microencephaly in the nNOS-/- mice, while this same dose caused no evident injury in the wild type mice. Thus, during development, a single exposure to alcohol can injure a genetically vulnerable brain, while it leaves a wild type brain unaffected. Since the genes that confer alcohol resistance and vulnerability in developing humans are unknown, any particular human fetus is potentially vulnerable. Thus, women should be counseled to consume no alcohol during pregnancy.

摘要

孕期母亲酗酒会损害胎儿大脑并导致胎儿酒精综合征(FAS)。尽管有公共警告劝阻孕期饮酒,但许多孕妇仍会间歇性饮酒,因为她们认为偶尔饮酒不会对胎儿有害。然而,由于基因差异,一些胎儿比其他胎儿更容易受到酒精所致脑损伤的影响。因此,相对少量的酒精对大多数胎儿可能无害,但却可能损害具有遗传易感性的胎儿。神经元型一氧化氮合酶(nNOS)可通过合成具有神经保护作用的一氧化氮来保护发育中的小鼠神经元免受酒精毒性影响。本研究检测了单次酒精暴露(在野生型小鼠中不会造成明显损伤)是否会损害nNOS基因缺陷小鼠(nNOS-/-小鼠)的大脑。野生型和nNOS-/-小鼠在出生后第4天(PD4)接受腹腔注射酒精(0.0、2.2或4.4mg/g体重),单次注射或在PD4 - 9期间每日重复注射。在PD10时测定海马体和大脑皮质内的脑容量和神经元数量。PD4 - 9期间的酒精暴露限制了两种品系小鼠的脑生长并导致神经元死亡,但nNOS-/-小鼠的小头畸形和神经元丢失的严重程度比野生型小鼠更严重。仅在PD4给予4.4mg/g的酒精剂量在nNOS-/-小鼠中导致了显著的神经元丢失和小头畸形,而相同剂量在野生型小鼠中未造成明显损伤。因此,在发育过程中,单次酒精暴露可损伤具有遗传易感性的大脑,而野生型大脑则不受影响。由于在发育中的人类中赋予酒精抗性和易感性的基因尚不清楚,任何特定的人类胎儿都可能具有易感性。因此,应建议女性在孕期不要饮酒。

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