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  • 标题:Acute and Chronic Effects of T-1032, a Novel Selective Phosphodiesterase Type 5 Inhibitor, on Monocrotaline-Induced Pulmonary Hypertension in Rats
  • 本地全文:下载
  • 作者:Hirotaka Inoue ; Koji Yano ; Tsunehisa Noto
  • 期刊名称:Biological and Pharmaceutical Bulletin
  • 印刷版ISSN:0918-6158
  • 电子版ISSN:1347-5215
  • 出版年度:2002
  • 卷号:25
  • 期号:11
  • 页码:1422-1426
  • DOI:10.1248/bpb.25.1422
  • 出版社:The Pharmaceutical Society of Japan
  • 摘要:We examined the hemodynamic property of T-1032 (methyl 2-(4-aminophenyl)-1,2-dihydro-1-oxo-7-(2-pyridylmethoxy)-4-(3,4,5-trimethoxy-phenyl)-3-isoquinoline carboxylate sulfate), a novel selective phosphodiesterase type 5 (PDE5) inhibitor, and evaluated the chronic effect of T-1032 on cardiac remodeling and its related death in monocrotaline (MCT)-induced pulmonary hypertensive rats. T-1032 (1, 10, 100 μg/kg, i.v.) significantly reduced mean arterial pressure (MAP) and right ventricular systolic pressure (RVSP) without a change in heart rate. The change in RVSP was more potent than that in MAP with 1 μg/kg T-1032 treatment (RVSP: −8.2±1.2%, mean arterial pressure: −5.7±1.2%), and reductions in RVSP and MAP reached a peak at doses of 1 and 10 μg/kg, respectively. In contrast, nitroglycerin (0.1, 1, 10 μg/kg, i.v.) and beraprost (0.1, 1 μg/kg, i.v.) did not cause a selective reduction in RVSP at any dose. When T-1032 (300 ppm in diet) was chronically administered, it delayed the death, and significantly suppressed right ventricular remodeling (T-1032-treated: 0.318±0.021 g, control: 0.401±0.013 g, p <0.05). Our present results suggest that T-1032 selectively reduces RVSP, and resulting in the suppression of right ventricular remodeling with a delay of the death in MCT-induced pulmonary hypertensive rats.
  • 关键词:phosphodiesterase type 5;monocrotaline rat;pulmonary hypertension
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