rdf:type |
|
lifeskim:mentions |
umls-concept:C0001613,
umls-concept:C0007776,
umls-concept:C0022655,
umls-concept:C0027882,
umls-concept:C0178696,
umls-concept:C0205245,
umls-concept:C0205345,
umls-concept:C0598958,
umls-concept:C1512474,
umls-concept:C1655731,
umls-concept:C1705241,
umls-concept:C1705242,
umls-concept:C2266853,
umls-concept:C2603343
|
pubmed:issue |
13
|
pubmed:dateCreated |
2007-6-21
|
pubmed:abstractText |
We compare the ability of two structurally different classes of epigenetic modulators, namely, histone deacetylase (HDAC) inhibitors containing either a hydroxamate or a mercaptoacetamide as the zinc binding group, to protect cortical neurons in culture from oxidative stress-induced death. This study reveals that some of the mercaptoacetamide-based HDAC inhibitors are fully protective, whereas the hydroxamates show toxicity at higher concentrations. Our present results appear to be consistent with the possibility that the mercaptoacetamide-based HDAC inhibitors interact with a different subset of the HDAC isozymes [less activity at HDAC1 and 2 correlates with less inhibitor toxicity], or alternatively, are interacting selectively with only the cytoplasmic HDACs that are crucial for protection from oxidative stress.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jun
|
pubmed:issn |
0022-2623
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:day |
28
|
pubmed:volume |
50
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
3054-61
|
pubmed:dateRevised |
2009-11-19
|
pubmed:meshHeading |
pubmed-meshheading:17539623-Acetamides,
pubmed-meshheading:17539623-Acetylation,
pubmed-meshheading:17539623-Animals,
pubmed-meshheading:17539623-Cell Survival,
pubmed-meshheading:17539623-Cells, Cultured,
pubmed-meshheading:17539623-Cerebral Cortex,
pubmed-meshheading:17539623-Epigenesis, Genetic,
pubmed-meshheading:17539623-Histone Deacetylase Inhibitors,
pubmed-meshheading:17539623-Histone Deacetylases,
pubmed-meshheading:17539623-Histones,
pubmed-meshheading:17539623-Hydroxamic Acids,
pubmed-meshheading:17539623-Isoenzymes,
pubmed-meshheading:17539623-Neurons,
pubmed-meshheading:17539623-Neuroprotective Agents,
pubmed-meshheading:17539623-Oxidative Stress,
pubmed-meshheading:17539623-Rats,
pubmed-meshheading:17539623-Rats, Sprague-Dawley,
pubmed-meshheading:17539623-Structure-Activity Relationship,
pubmed-meshheading:17539623-Sulfhydryl Compounds
|
pubmed:year |
2007
|
pubmed:articleTitle |
Functional differences in epigenetic modulators-superiority of mercaptoacetamide-based histone deacetylase inhibitors relative to hydroxamates in cortical neuron neuroprotection studies.
|
pubmed:affiliation |
Drug Discovery Program, Department of Medicinal Chemistry and Pharmacognosy, University of Illinois at Chicago, 833 South Wood Street, Chicago, Illinois 60612, USA. kozikowa@uic.edu
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|