Tsuji Ryozo, Fattori Vittorio, Abe Shin-ichi, Costa Lucio G, Kobayashi Kumiko
Environmental Health Science Laboratory, Sumitomo Chemical Co. Ltd., 3-1-98 Kasugade-Naka, Osaka 554-8559, Japan.
Neurotoxicol Teratol. 2008 May-Jun;30(3):228-36. doi: 10.1016/j.ntt.2008.01.004. Epub 2008 Jan 26.
Exposure to ethanol during development induces severe brain damage resulting in a number of CNS dysfunctions including microencephaly and mental retardation in humans and in laboratory animals. The most vulnerable period to ethanol neurotoxicity coincides with the peak of brain growth spurt. Recently, neurotrophic factors and/or their signal transduction pathways have been reported as a potential relevant target for the developmental neurotoxicity of ethanol. The present studies were designed to investigate the effects of ethanol given in various developmental phases during the brain growth spurt in rats. Rat pups were assigned to the three treatment groups and treated with 5 g/kg of ethanol for three days, on postnatal days (PND) 2-4, 6-8 or 13-15. Whole brain weights were reduced only in the PND 6-8 group concurrently with the reduction of GDNF mRNA in cortex in this group. BDNF mRNA expression was reduced in both the PND 6-8 and 13-15 groups, while mRNA expressions of NT-3 and NGF were unchanged in all three groups. Phospho-Akt level was mostly reduced in the PND 6-8 group. Both phospho-MAPK and p-70S6 kinase levels were decreased in all groups whereas no changes were observed in either phospho-PKCzeta or CREB level. The phosphorylation of Akt was immediately inhibited after single administration of ethanol, and its inhibition was correlated with variations in blood ethanol concentration. These findings suggest that GDNF and the phosphorylation of Akt play a possible key role in the ethanol-induced developmental neurotoxicity.
发育过程中接触乙醇会导致严重的脑损伤,在人类和实验动物中引发多种中枢神经系统功能障碍,包括小头畸形和智力迟钝。乙醇神经毒性最易受影响的时期与脑发育快速期的高峰期相吻合。最近,神经营养因子和/或其信号转导通路已被报道为乙醇发育神经毒性的潜在相关靶点。本研究旨在调查在大鼠脑发育快速期的不同发育阶段给予乙醇的影响。将幼鼠分为三个治疗组,在出生后第2 - 4天、6 - 8天或13 - 15天用5 g/kg乙醇处理三天。仅在出生后第6 - 8天的组中全脑重量降低,同时该组皮质中GDNF mRNA减少。出生后第6 - 8天和13 - 15天的组中BDNF mRNA表达均降低,而所有三组中NT - 3和NGF的mRNA表达均未改变。磷酸化Akt水平在出生后第6 - 8天的组中大多降低。所有组中磷酸化MAPK和p - 70S6激酶水平均降低,而磷酸化PKCzeta或CREB水平均未观察到变化。单次给予乙醇后,Akt的磷酸化立即受到抑制,其抑制与血液乙醇浓度的变化相关。这些发现表明GDNF和Akt的磷酸化在乙醇诱导的发育神经毒性中可能起关键作用。