In:
Circulation Research, Ovid Technologies (Wolters Kluwer Health), Vol. 105, No. 2 ( 2009-07-17), p. 194-200
Abstract:
Protein kinase (PK)Cα, PKCβ, and PKCγ comprise the conventional PKC isoform subfamily, which is thought to regulate cardiac disease responsiveness. Indeed, mice lacking the gene for PKC α show enhanced cardiac contractility and reduced susceptibility to heart failure. Recent data also suggest that inhibition of conventional PKC isoforms with Ro-32-0432 or Ro-31-8220 enhances heart function and antagonizes failure, although the isoform responsible for these effects is unknown. Here, we investigated mice lacking PKC α, PKC β, and PKC γ for effects on cardiac contractility and heart failure susceptibility. PKC α −/− mice, but not PKC βγ −/− mice, showed increased cardiac contractility, myocyte cellular contractility, Ca 2+ transients, and sarcoplasmic reticulum Ca 2+ load. PKCα −/− mice were less susceptible to heart failure following long-term pressure-overload stimulation or 4 weeks after myocardial infarction injury, whereas PKC βγ −/− mice showed more severe failure. Infusion of ruboxistaurin (LY333531), an orally available PKCα/β/γ inhibitor, increased cardiac contractility in wild-type and PKC βγ −/− mice, but not in PKC α −/− mice. More importantly, ruboxistaurin prevented death in wild-type mice throughout 10 weeks of pressure-overload stimulation, reduced ventricular dilation, enhanced ventricular performance, reduced fibrosis, and reduced pulmonary edema comparable to or better than metoprolol treatment. Ruboxistaurin was also administered to PKC βγ −/− mice subjected to pressure overload, resulting in less death and heart failure, implicating PKCα as the primary target of this drug in mitigating heart disease. As an aside, PKC αβγ triple-null mice showed no defect in cardiac hypertrophy following pressure-overload stimulation. In conclusion, PKCα functions distinctly from PKCβ and PKCγ in regulating cardiac contractility and heart failure, and broad-acting PKC inhibitors such as ruboxistaurin could represent a novel therapeutic approach in treating human heart failure.
Type of Medium:
Online Resource
ISSN:
0009-7330
,
1524-4571
DOI:
10.1161/CIRCRESAHA.109.195313
Language:
English
Publisher:
Ovid Technologies (Wolters Kluwer Health)
Publication Date:
2009
detail.hit.zdb_id:
1467838-X
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