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首页> 外文期刊>Brain pathology >Intrauterine exposure to dexamethasone impairs proliferation but not neuronal differentiation in the dentate gyrus of newborn common marmoset monkeys.
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Intrauterine exposure to dexamethasone impairs proliferation but not neuronal differentiation in the dentate gyrus of newborn common marmoset monkeys.

机译:宫内暴露于地塞米松会损害新生common猴的齿状回中的增殖,但不会损害神经元分化。

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摘要

Glucocorticoids applied prenatally alter birth weight and the maturation of the lungs. Moreover, glucocorticoids impair neuronal proliferation and differentiation in the hippocampal dentate gyrus. In the present study proliferation and neuronal differentiation in the dentate gyrus were studied in newborn common marmoset monkeys which were intrauterinely exposed to the synthetic glucocorticoid dexamethasone (DEX). Pregnant marmoset monkeys received DEX (5 mg/kg body weight) daily either during early (days 42-48) or late (days 90-96) pregnancy. In the hippocampi of newborn monkeys immunohistochemistry was performed with markers of proliferation (Ki-67), apoptosis (in situ tailing) as well as early and late neuronal differentiation (calretinin and calbindin). Both after early and late intrauterine exposure to DEX, proliferation of dentate gyrus cells was significantly decreased (P < 0.05). The density of apoptotic neurons was not altered by DEX treatment. Quantification of calretinin- and calbindin-immunoreactive neurons showed no significant differences between DEX-exposed and control animals. In conclusion, the proliferation of putative precursor cells but not the differentiation into mature cells was impaired in the dentate gyrus of newborn marmosets exposed intrauterinely to DEX.
机译:产前应用糖皮质激素会改变出生体重和肺部成熟度。此外,糖皮质激素损害海马齿状回中的神经元增殖和分化。在本研究中,研究了在子宫内暴露于合成糖皮质激素地塞米松(DEX)的新生newborn猴的齿状回中的增殖和神经元分化。怀孕的猴在怀孕的早期(第42-48天)或晚期(第90-96天)每天接受DEX(5 mg / kg体重)。在新生猴子的海马体中,使用增殖(Ki-67),凋亡(原位拖尾)以及早期和晚期神经元分化(钙黄蛋白和钙结合蛋白)的标记物进行免疫组织化学。子宫内早,晚暴露于DEX后,齿状回细胞的增殖均显着降低(P <0.05)。 DEX处理未改变凋亡神经元的密度。 Calretinin和calbindin免疫反应性神经元的定量显示,暴露于DEX的动物与对照动物之间无显着差异。总之,在子宫内暴露于DEX的新生mar猴的齿状回中,假定的前体细胞的增殖而不是向成熟细胞的分化受到损害。

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