Xiaoyu Wang
Medical School of Lishui University, No.1 Xueyuan Road, Lishui, 323000, Zhejiang, China,
Neurol Sci. 2015 Feb;36(2):289-95. doi: 10.1007/s10072-014-1934-y. Epub 2014 Oct 15.
In the current study effect of nicotine on expression of neurotrophins, brain-derived neurotrophic factor (BDNF) and nerve growth factor (NGF) has been studied in hippocampus and frontal cortex during development of brain in rats. Neurotrophins are factors that help in development of brain among which BDNF and NGF are very important, expressed at different stages during the developmental process. Different sedatives are reported to alter the expression of these factors. In this study, three groups of neonate rats (1-5, 5-10 and 10-15 days age) were used each having 20 rats. Ten were subjected to a dose of 66 μg of nicotine while other ten received the same amount of saline at the same time interval. Then expression of the BDNF and NGF was observed in hippocampus and frontal cortex tissue using immunoassay. Western blotting was used to observe the presence of BDNF in hippocampus as well as frontal cortex. In all groups there was a significant decrease in concentration of neurotrophic factors where nicotine was applied as compared to control. The highest expression of BDNF and NGF in hippocampus and frontal cortex was observed in 10-15 days group (G3) and in 5-10 group (G2) as compared to the control, P < 0.01. It was concluded that exposure of neonate rats to nicotine causes a decrease in the expression of NGF and BDNF and it effects the development of brain in neonates that can further impair brain functions.
在当前研究中,已对尼古丁对大鼠脑发育过程中海马体和额叶皮质中神经营养因子、脑源性神经营养因子(BDNF)和神经生长因子(NGF)表达的影响进行了研究。神经营养因子是有助于脑发育的因子,其中BDNF和NGF非常重要,在发育过程的不同阶段表达。据报道,不同的镇静剂会改变这些因子的表达。在本研究中,使用了三组新生大鼠(1 - 5日龄、5 - 10日龄和10 - 15日龄),每组20只。其中10只给予66μg尼古丁剂量,而另外10只在相同时间间隔接受等量的生理盐水。然后使用免疫测定法观察海马体和额叶皮质组织中BDNF和NGF的表达。使用蛋白质印迹法观察海马体以及额叶皮质中BDNF的存在情况。与对照组相比,在所有应用尼古丁的组中,神经营养因子的浓度均显著降低。与对照组相比,在10 - 15日龄组(G3)的海马体和额叶皮质以及5 - 10日龄组(G2)中观察到BDNF和NGF的最高表达,P < 0.01。得出的结论是,新生大鼠暴露于尼古丁会导致NGF和BDNF表达降低,并影响新生大鼠的脑发育,这可能会进一步损害脑功能。