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母体暴露于3,3'-亚氨基二丙腈会靶向海马颗粒细胞谱系的晚期分化,从而影响大鼠后代的脑源性神经营养因子信号传导和中间神经元亚群。

Maternal exposure to 3,3'-iminodipropionitrile targets late-stage differentiation of hippocampal granule cell lineages to affect brain-derived neurotrophic factor signaling and interneuron subpopulations in rat offspring.

作者信息

Itahashi Megu, Abe Hajime, Tanaka Takeshi, Mizukami Sayaka, Kikuchihara Yoh, Yoshida Toshinori, Shibutani Makoto

机构信息

Laboratory of Veterinary Pathology, Tokyo University of Agriculture and Technology, 3-5-8 Saiwai-cho, Fuchu-shi, Tokyo, 183-8509, Japan.

Pathogenetic Veterinary Science, United Graduate School of Veterinary Sciences, Gifu University, 1-1 Yanagido, Gifu-shi, Gifu, 501-1193, Japan.

出版信息

J Appl Toxicol. 2015 Aug;35(8):884-94. doi: 10.1002/jat.3086. Epub 2014 Nov 25.

Abstract

3,3'-Iminodipropionitrile (IDPN) causes neurofilament (NF)-filled swellings in the proximal segments of many large-caliber myelinated axons. This study investigated the effect of maternal exposure to IDPN on hippocampal neurogenesis in rat offspring using pregnant rats supplemented with 0 (controls), 67 or 200 ppm IDPN in drinking water from gestational day 6 to day 21 after delivery. On postnatal day (PND) 21, female offspring subjected to analysis had decreased parvalbumin(+), reelin(+) and phospho-TrkB(+) interneurons in the dentate hilus at 200 ppm and increased granule cell populations expressing immediate-early gene products, Arc or c-Fos, at ≥  67 ppm. mRNA expression in the dentate gyrus examined at 200 ppm decreased with brain-derived neurotrophic factor (Bdnf) and very low density lipoprotein receptor. Immunoreactivity for phosphorylated NF heavy polypeptide decreased in the molecular layer of the dentate gyrus and the stratum radiatum of the cornu ammonis (CA) 3, portions showing axonal projections from mossy cells and pyramidal neurons, at 200 ppm on PND 21, whereas immunoreactivity for synaptophysin was unchanged in the dentate gyrus. Observed changes all disappeared on PND 77. There were no fluctuations in the numbers of apoptotic cells, proliferating cells and subpopulations of granule cell lineage in the subgranular zone on PND 21 and PND 77. Thus, maternal IDPN exposure may reversibly affect late-stage differentiation of granule cell lineages involving neuronal plasticity as evident by immediate-early gene responses to cause BDNF downregulation resulting in a reduction in parvalbumin(+) or reelin(+) interneurons and suppression of axonal plasticity in the mossy cells and CA3 pyramidal neurons.

摘要

3,3'-亚氨基二丙腈(IDPN)会在许多大口径有髓轴突的近端段引发充满神经丝(NF)的肿胀。本研究利用在妊娠第6天至产后第21天给怀孕大鼠饮用添加0(对照组)、67或200 ppm IDPN的饮用水,来探究母体接触IDPN对大鼠后代海马神经发生的影响。在出生后第21天(PND 21),接受分析的雌性后代在200 ppm时齿状回门区的小白蛋白(+)、Reelin(+)和磷酸化TrkB(+)中间神经元减少,在≥67 ppm时表达即刻早期基因产物Arc或c-Fos的颗粒细胞群体增加。在200 ppm时检测到齿状回中的mRNA表达随脑源性神经营养因子(Bdnf)和极低密度脂蛋白受体而降低。在PND 21时,200 ppm下齿状回分子层和海马体(CA)3的辐射层中磷酸化NF重多肽的免疫反应性降低,这些部位显示有来自苔藓细胞和锥体神经元的轴突投射,而齿状回中突触素的免疫反应性未改变。观察到的变化在PND 77时全部消失。在PND 21和PND 77时,颗粒细胞谱系的凋亡细胞、增殖细胞数量以及颗粒下区亚群均无波动。因此,母体接触IDPN可能会可逆地影响颗粒细胞谱系的晚期分化,这涉及神经元可塑性,如通过即刻早期基因反应导致BDNF下调,从而导致小白蛋白(+)或Reelin(+)中间神经元减少以及苔藓细胞和CA3锥体神经元的轴突可塑性受到抑制。

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