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Activation of ATP-sensitive K+ channels by epoxyeicosatrienoic acids in rat cardiac ventricular myocytes

  • Tong Lu
    ,
  • Toshinori Hoshi
    ,
  • ,
  • Arthur A. Spector
    ,
  • Hon Chi Lee(corresponding author)
*Corresponding author for this work
  • University of Iowa
    ,
  • Departments of Molecular Physiology and Biophysics
    ,
  • ,
  • VA Medical Center
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

1. We examined the effects of epoxyeicosatrienoic acids (EETs), which are cytochrome P450 metabolites of arachidonic acid (AA), on the activities of the ATP-sensitive K+ (KATP) channels of rat cardiac myocytes, using the inside-out patch-clamp technique. 2. In the presence of 100 μM cytoplasmic ATP, the KATP channel open probability (Po) was increased by 240 ± 60% with 0.1 μM 11,12-EET and by 400 ± 54% with 5 μM 11,12-EET (n = 5-10, P < 0.05 vs. control), whereas neither 5 μM 11,12-dihydroxyeicosatrienoic acid (DHET), which is the epoxide hydrolysis product of 11,12-EET, had any effect on Po. 3. The half-maximal activating concentration (EC50) was 18.9 ± 2.6 nM for 11,12-EET (n = 5) and 19.1 ± 4.8 nM for 8,9-EET (n = 5, P = n.s. vs. 11,12-EET). Furthermore, 11,12-EET failed to alter the inhibition of KATP channels by glyburide. 4. Application of 11,12-EET markedly decreased the channel sensitivity to cytoplasmic ATP. The half-maximal inhibitory concentration of ATP (IC50) was increased from 21.2 ± 2.0 μM at baseline to 240 ± 60 μM with 0.1 μM 11,12-EET (n = 5, P < 0.05 vs. control) and to 780 ± 30 μM with 5 μM 11,12-EET (n = 11, P < 0.05 vs. control). 5. Increasing the ATP concentration increased the number of kinetically distinguishable closed states, promoting prolonged closure durations. 11,12-EET antagonized the effects of ATP on the kinetics of the KATP channels in a dose- and voltage-dependent manner. 11,12-EET (1 μM) reduced the apparent association rate constant of ATP to the channel by 135-fold. 6. Application of 5 μM 11,12-EET resulted in hyperpolarization of the resting membrane potential in isolated cardiac myocytes, which could be blocked by glyburide. 7. These results suggest that EETs are potent activators of the cardiac KATP channels, modulating channel behaviour by reducing the channel sensitivity to ATP. Thus, EETs could be important endogenous regulators of cardiac electrical excitability.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 811-827 (17 pages)

Journal (Volume, Issue Number)

Journal of Physiology (Volume 537, Issue 3)

Publication milestones

  • Published - 12/15/2001

Publication status

Published - 12/15/2001

ISSN

0022-3751

Publication IDs

  • Scopus: 0035893696
  • PubMed: 11744757

Publication metrics

Metrics

SciVal
citations
67
Scopus
citations
Fractional count
1
Fractional count
0.20
Fractional count
4
Fractional count
0.80
Fractional count
1
Fractional count
1
SciVal
FWCI
1.31
SciVal
Author count
5
SciVal
Paper percentile
89

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Funding Details

FunderFunding number
NHLBI
R01HL063754