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A unique mechanism of beta-blocker action: carvedilol stimulates beta-arrestin signaling.

Publication ,  Journal Article
Wisler, JW; DeWire, SM; Whalen, EJ; Violin, JD; Drake, MT; Ahn, S; Shenoy, SK; Lefkowitz, RJ
Published in: Proc Natl Acad Sci U S A
October 16, 2007

For many years, beta-adrenergic receptor antagonists (beta-blockers or betaAR antagonists) have provided significant morbidity and mortality benefits in patients who have sustained acute myocardial infarction. More recently, beta-adrenergic receptor antagonists have been found to provide survival benefits in patients suffering from heart failure, although the efficacy of different beta-blockers varies widely in this condition. One drug, carvedilol, a nonsubtype-selective betaAR antagonist, has proven particularly effective in the treatment of heart failure, although the mechanism(s) responsible for this are controversial. Here, we report that among 16 clinically relevant betaAR antagonists, carvedilol displays a unique profile of in vitro signaling characteristics. We observed that in beta2 adrenergic receptor (beta2AR)-expressing HEK-293 cells, carvedilol has inverse efficacy for stimulating G(s)-dependent adenylyl cyclase but, nonetheless, stimulates (i) phosphorylation of the receptor's cytoplasmic tail on previously documented G protein-coupled receptor kinase sites; (ii) recruitment of beta-arrestin to the beta2AR; (iii) receptor internalization; and (iv) activation of extracellular regulated kinase 1/2 (ERK 1/2), which is maintained in the G protein-uncoupled mutant beta2AR(T68F,Y132G,Y219A) (beta2AR(TYY)) and abolished by beta-arrestin2 siRNA. Taken together, these data indicate that carvedilol is able to stabilize a receptor conformation which, although uncoupled from G(s), is nonetheless able to stimulate beta-arrestin-mediated signaling. We hypothesize that such signaling may contribute to the special efficacy of carvedilol in the treatment of heart failure and may serve as a prototype for a new generation of therapeutic beta2AR ligands.

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Published In

Proc Natl Acad Sci U S A

DOI

ISSN

0027-8424

Publication Date

October 16, 2007

Volume

104

Issue

42

Start / End Page

16657 / 16662

Location

United States

Related Subject Headings

  • beta-Arrestins
  • Signal Transduction
  • Receptors, Adrenergic, beta-2
  • Propanolamines
  • Phosphorylation
  • Mitogen-Activated Protein Kinase 3
  • Mitogen-Activated Protein Kinase 1
  • Humans
  • Cell Line
  • Carvedilol
 

Citation

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Wisler, J. W., DeWire, S. M., Whalen, E. J., Violin, J. D., Drake, M. T., Ahn, S., … Lefkowitz, R. J. (2007). A unique mechanism of beta-blocker action: carvedilol stimulates beta-arrestin signaling. Proc Natl Acad Sci U S A, 104(42), 16657–16662. https://doi.org/10.1073/pnas.0707936104
Wisler, James W., Scott M. DeWire, Erin J. Whalen, Jonathan D. Violin, Matthew T. Drake, Seungkirl Ahn, Sudha K. Shenoy, and Robert J. Lefkowitz. “A unique mechanism of beta-blocker action: carvedilol stimulates beta-arrestin signaling.Proc Natl Acad Sci U S A 104, no. 42 (October 16, 2007): 16657–62. https://doi.org/10.1073/pnas.0707936104.
Wisler JW, DeWire SM, Whalen EJ, Violin JD, Drake MT, Ahn S, et al. A unique mechanism of beta-blocker action: carvedilol stimulates beta-arrestin signaling. Proc Natl Acad Sci U S A. 2007 Oct 16;104(42):16657–62.
Wisler, James W., et al. “A unique mechanism of beta-blocker action: carvedilol stimulates beta-arrestin signaling.Proc Natl Acad Sci U S A, vol. 104, no. 42, Oct. 2007, pp. 16657–62. Pubmed, doi:10.1073/pnas.0707936104.
Wisler JW, DeWire SM, Whalen EJ, Violin JD, Drake MT, Ahn S, Shenoy SK, Lefkowitz RJ. A unique mechanism of beta-blocker action: carvedilol stimulates beta-arrestin signaling. Proc Natl Acad Sci U S A. 2007 Oct 16;104(42):16657–16662.
Journal cover image

Published In

Proc Natl Acad Sci U S A

DOI

ISSN

0027-8424

Publication Date

October 16, 2007

Volume

104

Issue

42

Start / End Page

16657 / 16662

Location

United States

Related Subject Headings

  • beta-Arrestins
  • Signal Transduction
  • Receptors, Adrenergic, beta-2
  • Propanolamines
  • Phosphorylation
  • Mitogen-Activated Protein Kinase 3
  • Mitogen-Activated Protein Kinase 1
  • Humans
  • Cell Line
  • Carvedilol