It is known that cognitive processes, such as learning and memory, are affected in depression. Several authors
have described histone deacetylase (HDAC) inhibitors as a class of drugs that improve long-term memory formation. The
current study examined the effects of maternal deprivation (MD) and chronic mild stress (CMS), which have been shown
as animal models of depression, and the effects of sodium butyrate (SB), a HDAC inhibitor, on recognition memory.
Considering that neurotrophic factors have been pointed as a key event involved in cognition and depressive disorder,
levels of neurotrophic factors (BDNF, NGF and GDNF) were investigated. MD and CMS induced depressive-like
behavior in the forced swimming test (FST) and memory impairment in the object recognition (OR) test, without altering
locomotor activity of rats. In addition, SB was able to reverse the stress-induced neurotrophic factors decrease and
reversed memory impairment. The results indicate that stress both at early and later stage of life may induce cognitive
impairment in animals and neurotrophic factors (BDNF, NGF and GDNF) levels decrease. SB treatment improved the
recognition memory and reversed the neurotrophins levels decreased in the hippocampus of rats submitted to the MD and
CMS models. Together, our results reinforce the notion that SB displays a specific antidepressant profile and improves
cognition in MD and CMS rats that may be, at least in part, due to its upregulation of neurotrophic factors.
Keywords: BDNF, chronic mild stress, depression, GDNF, maternal deprivation, NGF, sodium butyrate.
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