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Research ArticleCARDIOVASCULAR

A Novel Chymase Inhibitor, 2-(5-Formylamino-6-oxo-2-phenyl-1,6-dihydropyrimidine-1-yl)-N-[{3,4-dioxo-1-phenyl-7-(2-pyridyloxy)}-2-heptyl]acetamide (NK3201), Suppressed Intimal Hyperplasia after Balloon Injury

Shinji Takai, Hiroshi Sakonjo, Kohzo Fukuda, Denan Jin, Masato Sakaguchi, Keiichi Kamoshita, Koichi Ishida, Yoshikazu Sukenaga and Mizuo Miyazaki
Journal of Pharmacology and Experimental Therapeutics February 2003, 304 (2) 841-844; DOI: https://doi.org/10.1124/jpet.102.042580
Shinji Takai
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Hiroshi Sakonjo
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Kohzo Fukuda
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Denan Jin
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Masato Sakaguchi
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Keiichi Kamoshita
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Koichi Ishida
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Yoshikazu Sukenaga
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Mizuo Miyazaki
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Abstract

In this study, we investigated whether an orally active chymase inhibitor, 2-(5-formylamino-6-oxo-2-phenyl-1,6-dihydropyrimidine-1-yl)-N-[{3,4-dioxo-1-phenyl-7-(2-pyridyloxy)}-2-heptyl]acetamide (NK3201), prevents intimal hyperplasia in carotid arteries injured by a balloon catheter in dog. Each dog was administered NK3201 (1 mg/kg per day, p.o.) or placebo beginning 5 days before balloon injury and continuing through the experiments. Four weeks after balloon injury, NK3201 did not affect the plasma renin and angiotensin-converting enzyme activities. The chymase activity was significantly increased in the injured arteries, whereas the angiotensin-converting enzyme activity was not. NK3201 significantly reduced the chymase activity in the injured arteries. The intimal area in the placebo- and NK3201-treated group and was 0.46 ± 0.06 and 0.24 ± 0.04 mm2, respectively, and this difference was significant. In this study, we demonstrated for the first time that a chymase inhibitor prevented the development of intimal hyperplasia in the balloon-injured arteries.

Footnotes

  • Supported by Grant-in-Aid 12770048 for Encouragement of Young Scientists from the Japanese Ministry of Education, Science, Sports, and Culture.

  • DOI: 10.1124/jpet.102.042580

  • Abbreviations:
    ACE
    angiotensin-converting enzyme
    AT1 receptor
    angiotensin II type 1 receptor
    NK3201
    2-(5-formylamino-6-oxo-2-phenyl-1,6-dihydropyrimidine-1-yl)-N-[{3,4-dioxo-1-phenyl-7-(2-pyridyloxy)}-2-heptyl]acetamide
    • Received August 1, 2002.
    • Accepted October 4, 2002.
  • The American Society for Pharmacology and Experimental Therapeutics
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Journal of Pharmacology and Experimental Therapeutics: 304 (2)
Journal of Pharmacology and Experimental Therapeutics
Vol. 304, Issue 2
1 Feb 2003
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Research ArticleCARDIOVASCULAR

A Novel Chymase Inhibitor, 2-(5-Formylamino-6-oxo-2-phenyl-1,6-dihydropyrimidine-1-yl)-N-[{3,4-dioxo-1-phenyl-7-(2-pyridyloxy)}-2-heptyl]acetamide (NK3201), Suppressed Intimal Hyperplasia after Balloon Injury

Shinji Takai, Hiroshi Sakonjo, Kohzo Fukuda, Denan Jin, Masato Sakaguchi, Keiichi Kamoshita, Koichi Ishida, Yoshikazu Sukenaga and Mizuo Miyazaki
Journal of Pharmacology and Experimental Therapeutics February 1, 2003, 304 (2) 841-844; DOI: https://doi.org/10.1124/jpet.102.042580

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Research ArticleCARDIOVASCULAR

A Novel Chymase Inhibitor, 2-(5-Formylamino-6-oxo-2-phenyl-1,6-dihydropyrimidine-1-yl)-N-[{3,4-dioxo-1-phenyl-7-(2-pyridyloxy)}-2-heptyl]acetamide (NK3201), Suppressed Intimal Hyperplasia after Balloon Injury

Shinji Takai, Hiroshi Sakonjo, Kohzo Fukuda, Denan Jin, Masato Sakaguchi, Keiichi Kamoshita, Koichi Ishida, Yoshikazu Sukenaga and Mizuo Miyazaki
Journal of Pharmacology and Experimental Therapeutics February 1, 2003, 304 (2) 841-844; DOI: https://doi.org/10.1124/jpet.102.042580
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