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首页> 外文期刊>Alcoholism: Clinical and experimental research >Prenatal Ethanol Exposure and Postnatal Environmental Intervention Alter Dopaminergic Neuron and Microglia Morphology in the Ventral Tegmental Area During Adulthood
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Prenatal Ethanol Exposure and Postnatal Environmental Intervention Alter Dopaminergic Neuron and Microglia Morphology in the Ventral Tegmental Area During Adulthood

机译:产前乙醇暴露和产后环境干预改变了多巴胺能神经元和在成年期间腹部的腹侧三核神经元和微胶质细胞形态

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Background Prenatal ethanol exposure (PE) impairs midbrain dopaminergic (DA) neuron function, which might contribute to various cognitive and behavioral deficits, including attention deficits and increased addiction risk, often observed in individuals with fetal alcohol spectrum disorders. Currently, the underlying mechanisms for PE‐induced deficits are unclear. PE could lead to neuroinflammation by activating microglia, which play an important role in synaptic function. In the present study, we investigated PE effects on microglial activation and DA neuron density and morphology in the ventral tegmental area (VTA). Since postnatal environmental enrichment can reduce neuroinflammation and ameliorate several PE‐induced behavioral deficits, we examined if a postnatal environmental intervention strategy using neonatal handling and postweaning complex housing could reverse PE effects on VTA DA neurons and microglia. Methods Pregnant rats received 0 or 6?g/kg/d ethanol by 2 intragastric intubations on gestation days 8 to 20. After birth, rats were reared in the standard laboratory or enriched condition. Male adult rats (8 to 12?weeks old) were used for immunocytochemistry. Results The results showed that PE decreased VTA DA neuron body size in standardly housed rats. Moreover, there was a significant decrease in numbers of VTA microglial branches and junctions in PE rats, suggesting morphological activation of microglia and possible neuroinflammation. The PE effects on microglia were normalized by postnatal environmental intervention, which also decreased the numbers of microglial branches and junctions in control animals, possibly via reduced stress. Conclusions Our findings show an association between PE‐induced morphological activation of microglia and impaired DA neuron morphology in the VTA. Importantly, postnatal environmental intervention rescues possible PE‐induced microglial activation. These data support that environmental intervention can be effective in ameliorating cognitive and behavioral deficits associated with VTA DA neuron dysfunctions, such as attention deficits and increased addiction risk.
机译:背景产前乙醇暴露(PE)损害中脑多巴胺能(DA)神经元功能,这可能导致各种认知和行为缺陷,包括注意力缺陷和增加的成瘾风险,通常在具有胎儿酒精谱系障碍的个体中观察到。目前,PE引起的赤字的潜在机制尚不清楚。 PE可以通过激活微胶质引起神经炎性炎症,在突触功能中起着重要作用。在本研究中,我们研究了对腹侧引物区域(VTA)中的显微胶质激活和DA神经元密度和形态的体育效应。由于产后环境富集可以减少神经引起的炎症和改善几种体育诱导的行为缺陷,我们检查了使用新生儿处理和切换复杂外壳的出生环境干预策略是否可以对VTA da神经元和小胶质细胞逆转体育效应。方法对妊娠日期8至20天的2个胃内插管接受0或6μl胃肠内插管的妊娠大鼠。出生后,大鼠在标准实验室或富集的病症中饲养。男性成年大鼠(8至12个?大岁月)用于免疫细胞化学。结果结果表明,PE在标准采集的大鼠中降低了VTA Da神经元体尺寸。此外,PE大鼠的VTA小胶质分支和结的数量显着降低,表明微凝血性的形态激活和可能的神经炎性炎症。通过产后环境干预对微胶质细胞进行标准化,这也降低了对照动物中的小胶质分支和交叉点的数量,可能通过降低应力。结论我们的研究结果表明,体育诱导的微胶质诱导的形态激活与VTA中的DA神经元形态受损之间的关联。重要的是,产后环境干预救出可能的体育诱导的小胶质激活。这些数据支持,环境干预可以有效地改善与VTA da Neuron功能障碍相关的认知和行为缺陷,例如注意缺陷和增加的成瘾风险。

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