Background: Emerging evidence suggests that epigenetic mechanisms are involved in different brain
functions such as the development of the nervous system and normal neuronal function. At the same time, it has
been proposed that several neurological diseases are in part, caused by aberrant epigenetic modifications. Nevertheless,
the mechanisms underlying pathological alterations in the brain genome are not completely understood.
Methods and Results: Post-transcriptional histone acetylation is a major mechanism of chromatin remodeling,
contributing to epigenetic regulation of gene transcription. Histone deacetylases (HDACs) are a family of proteins
involved in both physiological and pathological conditions by regulating the status of chromatin histone acetylation.
It is now becoming clear that epigenetic regulatory mechanisms may also play a major role in epilepsy;
modulation of chromatin structure through histone modifications has emerged as an important regulator of gene
transcription in the brain and altered histone acetylation seems to contribute to changes in gene expression associated
with epilepsy and the epileptogenic process. Histone modification is crucial for regulating neurobiological
processes such as neural network function, synaptic plasticity, and synaptogenesis which also contribute to the
pathophysiology of epilepsy.
Conclusions: The role of epigenetics in epilepsy development is a new and emerging research area; the present
article reviews the recent findings on the role played by HDACs and the possible function of different histone
modifications in epilepsy and epileptogenesis. Inhibitors of HDACs (HDACIs) have been tested in different experimental
models of epilepsy with some success. We also review the results from these studies, which indicate
HDACIs as potential new therapeutic agents for the treatment of human epilepsy.