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Rho-kinase as a potential target for the treatment of erectile dysfunction

  • Kanchan Chitaley(corresponding author)
    ,
  • R. Clinton Webb
    ,
  • Thomas M. Mills
*Corresponding author for this work
  • University of Michigan, Ann Arbor
Scholary Output:
Contribution to journal
Article
Peer-review

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Erectile dysfunction is a condition that is estimated to affect more than 30 million men in the United States alone. The prevalence of erectile dysfunction is increased with age and is often secondary to diseases such as depression, hypertension and diabetes. Causes of erectile dysfunction include physical injury to the cavernosum and abnormal cerebral and peripheral nervous system functioning. However, many cases of erectile dysfunction are the result of dysfunctional signaling in the cavernosal vasculature. This article will detail the important role of a vasoconstrictor mechanism mediated by the small G-protein RhoA and a downstream serine/threonine kinase, Rho-kinase, in the maintenance of penile flaccidity. Recent evidence demonstrates that inhibition of endogenous Rho-kinase initiates an erectile response in an in vivo rat model. These initial findings introduce a novel potential therapeutic approach for the treatment of erectile dysfunction.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 601-606 (6 pages)

Journal (Volume, Issue Number)

Drug News and Perspectives (Volume 14, Issue 10)

Publication milestones

  • Published - 2001

Publication status

Published - 2001

ISSN

0214-0934

Publication IDs

  • Scopus: 0035724390
  • PubMed: 12806426

Publication metrics

Metrics

SciVal
citations
18
Fractional count
1
Fractional count
0.33
Fractional count
2
Fractional count
0.67
Fractional count
1
Fractional count
1
SciVal
FWCI
0.15
SciVal
Author count
3
SciVal
Paper percentile
68
Scopus
citations

PlumX

Citation count
20
Captures
18