Department of Primary Child Health Care, Children's Hospital of Chongqing Medical University, Chongqing, P.R. China; Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing, P.R. China; China International Science and Technology Cooperation base of Child development and Critical Disorders, Chongqing Key Laboratory of Pediatrics, Chongqing, P.R. China.
Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing, P.R. China; China International Science and Technology Cooperation base of Child development and Critical Disorders, Chongqing Key Laboratory of Pediatrics, Chongqing, P.R. China.
J Nutr Biochem. 2017 Sep;47:75-85. doi: 10.1016/j.jnutbio.2017.05.007. Epub 2017 May 25.
This study investigated the prenatal marginal vitamin A deficiency (mVAD)-related impairment in learning and memory and the interactions between RARα, Src and NR1. Learning and memory were assessed in adult rats that were exposed to prenatal mVAD with Morris water maze. The average escape time was longer in mVAD rats, and they passed the hidden platform fewer times during the memory retention test than normal vitamin A intake (VAN) rats. The mRNA and protein levels of RARα, Src and NR1 in mVAD rats were significantly lower than those in VAN rats. RARα and Src, but not NR1, were in the same protein complex. RA treatment-induced increase in RARα, Src and NR1 expressions in mVAD neurons was much lower than that in VAN neurons. Overexpression of RARα gene in VAN neurons induced an increase in RARα, Src and NR1 expressions, while silencing of RARα gene induced a decrease in expressions of RARα and Src, but not that of of NR1. In mVAD neurons, however, overexpression of RARα did not induce an increase in NR1 expression, while silencing of RARα gene had no effect on Src and NR1 expressions. Furthermore, inhibition of Src was associated with a decrease in NR1 expression but not that of RARα. Prenatal mVAD was associated with impaired learning and memory in adult rats. It is possible that mVAD-related decrease in RARα led to a decrease in Src expression, which in turn down-regulated NR1 expression and Ca influx and eventually caused learning and memory deficits.
本研究探讨了产前边缘维生素 A 缺乏症 (mVAD) 对学习和记忆的损害,以及 RARα、Src 和 NR1 之间的相互作用。采用 Morris 水迷宫对暴露于产前 mVAD 的成年大鼠进行学习和记忆评估。mVAD 大鼠的平均逃逸时间较长,在记忆保留测试中通过隐藏平台的次数少于正常维生素 A 摄入 (VAN) 大鼠。mVAD 大鼠的 RARα、Src 和 NR1 的 mRNA 和蛋白水平明显低于 VAN 大鼠。RARα 和 Src,但不是 NR1,位于同一蛋白质复合物中。RA 处理诱导 mVAD 神经元中 RARα、Src 和 NR1 表达的增加远低于 VAN 神经元。VAN 神经元中 RARα 基因的过表达诱导 RARα、Src 和 NR1 表达的增加,而 RARα 基因的沉默诱导 RARα 和 Src 的表达减少,但 NR1 的表达没有减少。然而,在 mVAD 神经元中,过表达 RARα 不会诱导 NR1 表达增加,而沉默 RARα 基因对 Src 和 NR1 表达没有影响。此外,Src 的抑制与 NR1 表达的减少有关,但与 RARα 的减少无关。产前 mVAD 与成年大鼠学习和记忆受损有关。可能是 mVAD 相关的 RARα 减少导致 Src 表达减少,进而下调 NR1 表达和 Ca 内流,最终导致学习和记忆缺陷。