Food Bioactive HDAC Inhibitors in the Epigenetic Regulation of Heart Failure

Approximately 5.7 million U.S. adults have been diagnosed with heart failure (HF). More concerning is that one in nine U.S. deaths included HF as a contributing cause. Current HF drugs (e.g., β-blockers, ACEi) target intracellular signaling cascades downstream of cell surface receptors to p...

Full description

Bibliographic Details
Main Authors: Levi W. Evans, Bradley S. Ferguson
Format: Article
Language:English
Published: MDPI AG 2018-08-01
Series:Nutrients
Subjects:
Online Access:http://www.mdpi.com/2072-6643/10/8/1120
id doaj-6a62357b07e04e5fb5b3a12324b0baca
record_format Article
spelling doaj-6a62357b07e04e5fb5b3a12324b0baca2020-11-25T01:03:13ZengMDPI AGNutrients2072-66432018-08-01108112010.3390/nu10081120nu10081120Food Bioactive HDAC Inhibitors in the Epigenetic Regulation of Heart FailureLevi W. Evans0Bradley S. Ferguson1Department of Agriculture, Nutrition, & Veterinary Sciences, University of Nevada, Reno, NV 89557, USADepartment of Agriculture, Nutrition, & Veterinary Sciences, University of Nevada, Reno, NV 89557, USAApproximately 5.7 million U.S. adults have been diagnosed with heart failure (HF). More concerning is that one in nine U.S. deaths included HF as a contributing cause. Current HF drugs (e.g., β-blockers, ACEi) target intracellular signaling cascades downstream of cell surface receptors to prevent cardiac pump dysfunction. However, these drugs fail to target other redundant intracellular signaling pathways and, therefore, limit drug efficacy. As such, it has been postulated that compounds designed to target shared downstream mediators of these signaling pathways would be more efficacious for the treatment of HF. Histone deacetylation has been linked as a key pathogenetic element for the development of HF. Lysine residues undergo diverse and reversible post-translational modifications that include acetylation and have historically been studied as epigenetic modifiers of histone tails within chromatin that provide an important mechanism for regulating gene expression. Of recent, bioactive compounds within our diet have been linked to the regulation of gene expression, in part, through regulation of the epi-genome. It has been reported that food bioactives regulate histone acetylation via direct regulation of writer (histone acetyl transferases, HATs) and eraser (histone deacetylases, HDACs) proteins. Therefore, bioactive food compounds offer unique therapeutic strategies as epigenetic modifiers of heart failure. This review will highlight food bio-actives as modifiers of histone deacetylase activity in the heart.http://www.mdpi.com/2072-6643/10/8/1120heart failurehistone deacetylaseHDACHDAC inhibitorsfood bio-activesphytochemicals
collection DOAJ
language English
format Article
sources DOAJ
author Levi W. Evans
Bradley S. Ferguson
spellingShingle Levi W. Evans
Bradley S. Ferguson
Food Bioactive HDAC Inhibitors in the Epigenetic Regulation of Heart Failure
Nutrients
heart failure
histone deacetylase
HDAC
HDAC inhibitors
food bio-actives
phytochemicals
author_facet Levi W. Evans
Bradley S. Ferguson
author_sort Levi W. Evans
title Food Bioactive HDAC Inhibitors in the Epigenetic Regulation of Heart Failure
title_short Food Bioactive HDAC Inhibitors in the Epigenetic Regulation of Heart Failure
title_full Food Bioactive HDAC Inhibitors in the Epigenetic Regulation of Heart Failure
title_fullStr Food Bioactive HDAC Inhibitors in the Epigenetic Regulation of Heart Failure
title_full_unstemmed Food Bioactive HDAC Inhibitors in the Epigenetic Regulation of Heart Failure
title_sort food bioactive hdac inhibitors in the epigenetic regulation of heart failure
publisher MDPI AG
series Nutrients
issn 2072-6643
publishDate 2018-08-01
description Approximately 5.7 million U.S. adults have been diagnosed with heart failure (HF). More concerning is that one in nine U.S. deaths included HF as a contributing cause. Current HF drugs (e.g., β-blockers, ACEi) target intracellular signaling cascades downstream of cell surface receptors to prevent cardiac pump dysfunction. However, these drugs fail to target other redundant intracellular signaling pathways and, therefore, limit drug efficacy. As such, it has been postulated that compounds designed to target shared downstream mediators of these signaling pathways would be more efficacious for the treatment of HF. Histone deacetylation has been linked as a key pathogenetic element for the development of HF. Lysine residues undergo diverse and reversible post-translational modifications that include acetylation and have historically been studied as epigenetic modifiers of histone tails within chromatin that provide an important mechanism for regulating gene expression. Of recent, bioactive compounds within our diet have been linked to the regulation of gene expression, in part, through regulation of the epi-genome. It has been reported that food bioactives regulate histone acetylation via direct regulation of writer (histone acetyl transferases, HATs) and eraser (histone deacetylases, HDACs) proteins. Therefore, bioactive food compounds offer unique therapeutic strategies as epigenetic modifiers of heart failure. This review will highlight food bio-actives as modifiers of histone deacetylase activity in the heart.
topic heart failure
histone deacetylase
HDAC
HDAC inhibitors
food bio-actives
phytochemicals
url http://www.mdpi.com/2072-6643/10/8/1120
work_keys_str_mv AT leviwevans foodbioactivehdacinhibitorsintheepigeneticregulationofheartfailure
AT bradleysferguson foodbioactivehdacinhibitorsintheepigeneticregulationofheartfailure
_version_ 1725201712249044992