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Enhanced relaxation to the Rho-kinase inhibitor Y-27632 in mesenteric arteries from mineralocorticoid hypertensive rats

  • Davis S. Weber(corresponding author)
    ,
  • R. Clinton Webb
*Corresponding author for this work
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

Increased vasoconstriction is characteristic of hypertension. In this study, we tested the hypothesis that changes in vascular responses during mineralocorticoid hypertension may be due to increased activation of the Rho/Rho-kinase pathway. To test this, relaxation responses to the Rho-kinase inhibitor Y-27632 were determined by measuring isometric force in deendothelialized mesenteric arteries from mineralocorticoid-hypertensive rats and sham-operated controls. Following agonist-induced contraction by serotonin (5-HT, 5-hydroxytryptamine), arteries from hypertensive rats demonstrated a greater relaxation to the Rho-kinase inhibitor Y-27632 (65 ± 5% vs.28 ± 10%). Treatment with an EC50 concentration of Y-27632 following a KCl-induced contraction caused minimal relaxation of arteries in both groups of animals. These findings suggest that augmented Rho-kinase activity in the vasculature of mineralocorticoid hypertensive rats may contribute to the enhanced vascular reactivity of agonist-mediated stimuli characteristic of this model of hypertension.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 129-133 (5 pages)

Journal (Volume, Issue Number)

Pharmacology (Volume 63, Issue 3)

Publication milestones

  • Published - 2001

Publication status

Published - 2001

ISSN

0031-7012

Publication IDs

  • Scopus: 0035742442
  • PubMed: 11598417

Publication metrics

Metrics

SciVal
FWCI
2.20
SciVal
Author count
2
SciVal
citations
45
SciVal
Paper percentile
84
Fractional count
1
Fractional count
0.50
Fractional count
1
Fractional count
0.50
Fractional count
1
Fractional count
1
Scopus
citations

PlumX, opens in new tab

Citation count
45
Captures
10

Funding Details

FunderFunding number
NHLBI
P01HL018575