Adolescent intermittent ethanol use in male rats do not change cerebellar cell numbers but initiate astroglial reaction

IF 1.7 4区 医学 Q3 DEVELOPMENTAL BIOLOGY
Nurhan Çon, Sevcan Mercan, Asuman Küçüköner, Nüket Çalişkan
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引用次数: 0

Abstract

Alcohol consumption during adolescence causes negative structural changes in the cerebellum and can lead to cognitive and motor skill disorders. Unfortunately, the age at which individuals begin drinking alcohol has decreased in recent years, which has drawn attention to the effects of alcohol on neurological changes during preadolescence. In this study, we investigated the effects of adolescent intermittent ethanol (AIE) exposure on the cellular composition of the cerebellum in male rats, particularly when alcohol consumption begins early. The male rats received eight doses of intermittent intraperitoneal injection of 25% (v/v) ethanol (3 g/kg) or saline from postnatal days (PND) 25 to PND 38. In rats, 28–42 days old corresponds to 10–18 years old in humans. Two hours after the last injection, the cells, neurons, and non-neuronal cells in the cerebellum were immunocytochemically labeled and the total numbers of related cells were calculated using the Isotropic Fractionator method. We found that AIE exposure does not change the cell numbers of the cerebellum in the short term, but it does activate astrocytes in the white matter of the cerebellum. These findings suggest that alcohol use during adolescence impairs the innate immune system and negatively affects brain plasticity.

Abstract Image

Abstract Image

雄性大鼠青春期间歇使用乙醇不会改变小脑细胞数量,但会引发星形胶质细胞反应。
青春期饮酒会引起小脑结构的负面变化,并可能导致认知和运动技能障碍。遗憾的是,近年来开始饮酒的年龄有所下降,这引起了人们对青春期前酒精对神经系统变化影响的关注。在这项研究中,我们调查了青春期间歇性乙醇暴露(AIE)对雄性大鼠小脑细胞组成的影响,尤其是在饮酒开始较早的情况下。雄性大鼠从出生后第25天到第38天接受了8次间歇性腹腔注射25%(v/v)乙醇(3克/千克)或生理盐水。大鼠出生后 28-42 天相当于人类的 10-18 岁。最后一次注射两小时后,对小脑细胞、神经元和非神经元细胞进行免疫细胞化学标记,并使用等向分化法计算相关细胞的总数。我们发现,短期内接触 AIE 不会改变小脑细胞的数量,但会激活小脑白质中的星形胶质细胞。这些研究结果表明,青春期饮酒会损害先天性免疫系统,并对大脑的可塑性产生负面影响。
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来源期刊
CiteScore
3.30
自引率
5.60%
发文量
78
审稿时长
6-12 weeks
期刊介绍: International Journal of Developmental Neuroscience publishes original research articles and critical review papers on all fundamental and clinical aspects of nervous system development, renewal and regeneration, as well as on the effects of genetic and environmental perturbations of brain development and homeostasis leading to neurodevelopmental disorders and neurological conditions. Studies describing the involvement of stem cells in nervous system maintenance and disease (including brain tumours), stem cell-based approaches for the investigation of neurodegenerative diseases, roles of neuroinflammation in development and disease, and neuroevolution are also encouraged. Investigations using molecular, cellular, physiological, genetic and epigenetic approaches in model systems ranging from simple invertebrates to human iPSC-based 2D and 3D models are encouraged, as are studies using experimental models that provide behavioural or evolutionary insights. The journal also publishes Special Issues dealing with topics at the cutting edge of research edited by Guest Editors appointed by the Editor in Chief. A major aim of the journal is to facilitate the transfer of fundamental studies of nervous system development, maintenance, and disease to clinical applications. The journal thus intends to disseminate valuable information for both biologists and physicians. International Journal of Developmental Neuroscience is owned and supported by The International Society for Developmental Neuroscience (ISDN), an organization of scientists interested in advancing developmental neuroscience research in the broadest sense.
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