Abstract
Hexamethylenebisacetamide (HMBA) selectively and reversibly inhibited proliferation of human and rat vascular smooth-muscle cells (VSMCs) compared with endothelial cells, fibroblasts or lymphocytes. Half-maximal inhibition of VSMC proliferation occurred at 2-5 mM-HMBA, and at 30- greater than 50 mM for other cell types. HMBA also prevented de-differentiation, defined by the loss of smooth-muscle-specific myosin heavy chain, of primary rat VSMCs and caused partial re-differentiation of subcultured cells. Other inhibitors of ADP-ribosyltransferase were also selective inhibitors of VSMC proliferation.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Acetamides / pharmacology*
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Animals
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Cell Division / drug effects
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Cells, Cultured
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Coumarins / pharmacology
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DNA Replication / drug effects
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Endothelium, Vascular / cytology
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Endothelium, Vascular / drug effects
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Fibroblasts / cytology
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Fibroblasts / drug effects
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Hematinics / pharmacology*
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Humans
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Kinetics
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Muscle, Smooth, Vascular / cytology*
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Muscle, Smooth, Vascular / drug effects
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Quinazolines / pharmacology
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Quinazolinones
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Rats
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Thymidine / metabolism
Substances
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Acetamides
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Coumarins
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Hematinics
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Quinazolines
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Quinazolinones
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4-hydroxyquinazoline
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coumarin
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hexamethylene bisacetamide
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Thymidine