Brain Susceptibility to Methyl Donor Deficiency: From Fetal Programming to Aging Outcome in Rats

Int J Mol Sci. 2019 Nov 14;20(22):5692. doi: 10.3390/ijms20225692.

Abstract

Deficiencies in methyl donors, folate, and vitamin B12 are known to lead to brain function defects. Fetal development is the most studied but data are also available for such an impact in elderly rats. To compare the functional consequences of nutritional deficiency in young versus adult rats, we monitored behavioral outcomes of cerebellum and hippocampus circuits in the offspring of deficient mother rats and in adult rats fed a deficient diet from 2 to 8 months-of-age. We present data showing that the main deleterious consequences are found in young ages compared to adult ones, in terms of movement coordination and learning abilities. Moreover, we obtained sex and age differences in the deleterious effects on these functions and on neuronal layer integrity in growing young rats, while deficient adults presented only slight functional alterations without tissue damage. Actually, the cerebellum and the hippocampus develop and maturate according to different time lap windows and we demonstrate that a switch to a normal diet can only rescue circuits that present a long permissive window of time, such as the cerebellum, whereas the hippocampus does not. Thus, we argue, as others have, for supplements or fortifications given over a longer time than the developmental period.

Keywords: brain development; fetal programming; functional deficits; long-term effects; neuroplasticity.

MeSH terms

  • Animals
  • Brain / metabolism*
  • Brain / physiopathology*
  • Cognition
  • Deficiency Diseases / complications*
  • Deficiency Diseases / etiology
  • Deficiency Diseases / metabolism*
  • Diet
  • Disease Models, Animal
  • Female
  • Fetal Development*
  • Folic Acid Deficiency / complications
  • Folic Acid Deficiency / metabolism
  • Hippocampus / metabolism
  • Hippocampus / physiopathology
  • Male
  • Maze Learning
  • Neurodevelopmental Disorders / etiology*
  • Neurodevelopmental Disorders / metabolism*
  • Rats