Welch J H, Mayfield J J, Leibowitz A L, Baculis B C, Valenzuela C F
Department of Neurosciences, School of Medicine, University of New Mexico Health Sciences Center, Albuquerque, NM 87131, USA.
Department of Neurosciences, School of Medicine, University of New Mexico Health Sciences Center, Albuquerque, NM 87131, USA.
Neuroscience. 2016 Jun 2;324:107-18. doi: 10.1016/j.neuroscience.2016.03.004. Epub 2016 Mar 8.
Exposure to ethanol during fetal development produces long-lasting neurobehavioral deficits caused by functional alterations in neuronal circuits across multiple brain regions. Therapeutic interventions currently used to treat these deficits are only partially efficacious, which is a consequence of limited understanding of the mechanism of action of ethanol. Here, we describe a novel effect of ethanol in the developing brain. Specifically, we show that exposure of rats to ethanol in vapor chambers during the equivalent to the third trimester of human pregnancy causes brain micro-hemorrhages. This effect was observed both at low and high doses of ethanol vapor exposure, and was not specific to this exposure paradigm as it was also observed when ethanol was administered via intra-esophageal gavage. The vast majority of the micro-hemorrhages were located in the cerebral cortex but were also observed in the hypothalamus, midbrain, olfactory tubercle, and striatum. The auditory, cingulate, insular, motor, orbital, retrosplenial, somatosensory, and visual cortices were primarily affected. Immunohistochemical experiments showed that the micro-hemorrhages caused neuronal loss, as well as reactive astrogliosis and microglial activation. Analysis with the Catwalk test revealed subtle deficits in motor function during adolescence/young adulthood. In conclusion, our study provides additional evidence linking developmental ethanol exposure with alterations in the fetal cerebral vasculature. Given that this effect was observed at moderate levels of ethanol exposure, our findings lend additional support to the recommendation that women abstain from consuming alcoholic beverages during pregnancy.
胎儿发育期间接触乙醇会导致持久的神经行为缺陷,这是由多个脑区神经回路的功能改变引起的。目前用于治疗这些缺陷的治疗干预措施仅部分有效,这是由于对乙醇作用机制的了解有限。在此,我们描述了乙醇在发育中大脑的一种新作用。具体而言,我们发现,在相当于人类妊娠晚期的阶段,将大鼠置于蒸汽室中接触乙醇会导致脑微出血。在低剂量和高剂量乙醇蒸汽暴露下均观察到这种效应,并且这种效应并非这种暴露模式所特有,因为通过食管内灌胃给予乙醇时也观察到了这种效应。绝大多数微出血位于大脑皮层,但在下丘脑、中脑、嗅结节和纹状体中也观察到了。听觉、扣带回、岛叶、运动、眶额、压后皮质、体感和视觉皮层主要受到影响。免疫组织化学实验表明,微出血导致神经元丢失,以及反应性星形胶质细胞增生和小胶质细胞活化。通过Catwalk测试分析发现,在青春期/成年早期运动功能存在细微缺陷。总之,我们的研究提供了更多证据,将发育期间接触乙醇与胎儿脑血管系统的改变联系起来。鉴于在适度乙醇暴露水平下观察到了这种效应,我们的研究结果进一步支持了关于女性在怀孕期间应戒酒的建议。