Fattori Vittorio, Abe Shin-ichi, Kobayashi Kumiko, Costa Lucio G, Tsuji Ryozo
Environmental Health Science Laboratory, Sumitomo Chemical Co. Ltd., 3-1-98 Kasugade-Naka, Konohana-Ku, Osaka 554-8558, Japan.
J Appl Toxicol. 2008 Apr;28(3):370-6. doi: 10.1002/jat.1288.
Exposure to ethanol during development induces severe brain damage, resulting in a number of CNS dysfunctions including microencephaly and mental retardation. Potential targets of ethanol-induced neurotoxicity include neurotrophic factors and their signal transduction pathways. In the present study, rat pups were given ethanol at the dose of 5 g kg(-1) via gavage from postnatal day (PND) 5 to 8, and mRNA expression of nerve growth-factor (NGF), brain-derived neurotrophic factor (BDNF), and neurotrophic factor-3 (NT-3) in the cerebral cortex was examined, with attention to signal transduction, on PND 8. The mRNA level of BDNF was decreased by ethanol while those of NGF or NT-3 were not changed. Brain weights were decreased and the levels of phospho-MAPK, phospho-p70S6K and phospho Akt were decreased while phosphor-PKCzeta and phospho-CREB remained unchanged. These results suggest that BDNF and its related signal pathways involving Akt, MAPK and p70S6K are potential targets of ethanol-induced developmental neurotoxicity.
发育过程中接触乙醇会导致严重的脑损伤,引发包括小头畸形和智力迟钝在内的多种中枢神经系统功能障碍。乙醇诱导的神经毒性的潜在靶点包括神经营养因子及其信号转导途径。在本研究中,从出生后第5天(PND)至第8天,通过灌胃给幼鼠施用剂量为5 g kg(-1)的乙醇,并在PND 8时检测大脑皮层中神经生长因子(NGF)、脑源性神经营养因子(BDNF)和神经营养因子-3(NT-3)的mRNA表达,并关注信号转导情况。乙醇使BDNF的mRNA水平降低,而NGF或NT-3的mRNA水平未发生变化。脑重量减轻,磷酸化MAPK、磷酸化p70S6K和磷酸化Akt的水平降低,而磷酸化PKCzeta和磷酸化CREB保持不变。这些结果表明,BDNF及其涉及Akt、MAPK和p70S6K的相关信号通路是乙醇诱导的发育性神经毒性的潜在靶点。