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Impact of prenatal nicotine on the structure of midbrain dopamine regions in the rat

机译:产前尼古丁对大鼠中脑多巴胺区结构的影响

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In utero exposure of rats to nicotine (NIC) provides a useful animal model for studying the impact of smoking during pregnancy on human offspring. Certain sequelae of prenatal NIC exposure suggest an impact on the development of the midbrain dopamine (DA) system, which receives a robust cholinergic innervation from the mesopontine tegmentum. We therefore investigated whether prenatal NIC induced structural changes in cells and synapses within the midbrain that persisted into adulthood. Osmotic minipumps delivering either sodium bitartrate (vehicle; VEH) or NIC bitartrate at 2 mg/kg/day were implanted into nine timed-pregnant dams at E4. At birth, rat pups were culled to litters of six males each, and the litters were cross-fostered. Plasma levels of NIC and cotinine from killed pups provided evidence of NIC exposure in utero. Pups separated from dams at weaning showed a trend toward reduced locomotor activity at this time point but not when tested again in adulthood. Adult rats were killed for anatomical studies. Estimates of brain size and volume did not vary with NIC treatment. Midbrain sections stained for Nissl or by immunoperoxidase for tyrosine hydroxylase and analyzed using unbiased stereology revealed no changes in volume or cell number in the substantia nigra compacta or ventral tegmental area as a result of NIC exposure. Within the ventral tegmental area, electron microscopic physical disector analysis showed no significant differences in the number of axon terminals or the number of asymmetric (putative excitatory) or symmetric (putative inhibitory) synapses. Although too infrequent to estimate by unbiased stereology, no obvious difference in the proportion of cholinergic axons was noted in NIC-versus VEH-treated animals. These data suggest that activation of nicotinic receptors during prenatal development induces no significant modifications in the structure of cells in the ventral midbrain when assessed in adulthood.
机译:在大鼠子宫内暴露于尼古丁(NIC)提供了有用的动物模型,用于研究怀孕期间吸烟对人类后代的影响。产前NIC暴露的某些后遗症对中脑多巴胺(DA)系统的发育有影响,该系统从中桥蛋白被膜吸收了强大的胆碱能。因此,我们调查了产前NIC是否会诱导持续到成年的中脑内细胞和突触的结构变化。以2 mg / kg / day的剂量输送酒石酸氢钠(车辆; VEH)或NIC酒石酸氢盐的渗透微型泵植入E4处的9个定时怀孕大坝中。出生时,将幼鼠逐出,每只由六只雄性的仔仔淘汰,然后将仔仔杂交。被杀死幼犬的血浆NIC和可替宁水平为子宫内NIC暴露提供了证据。在断奶时与水坝分离的幼仔在这个时间点表现出运动能力降低的趋势,但成年后再次进行测试时则没有。将成年大鼠处死以进行解剖学研究。脑大小和容量的估计值随NIC治疗而变化。中脑切片进行Nissl染色或酪氨酸羟化酶用免疫过氧化物酶染色,并使用无偏见的立体分析进行分析,结果显示,由于NIC暴露,黑质致密部或腹侧被盖区的体积或细胞数均未发生变化。在腹侧被盖区,电子显微镜的物理解剖学分析显示,在轴突末端的数量或不对称(假定兴奋性)或对称(假定抑制性)突触的数量上没有显着差异。尽管不太经常通过无偏见的立体学进行估计,但在NIC与VEH处理的动物中,胆碱能轴突的比例没有明显差异。这些数据表明,在成年期进行评估时,产前发育过程中烟碱样受体的激活不会引起腹中脑细胞结构的显着改变。

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