Roh Hui-Yul, Jung In-Sang, Park Jung-Woo, Yun Yeo-Pyo, Yi Kyu-Yang, Yoo Sung-Eun, Kwon Suk-Hyung, Chung Hun-Jong, Shin Hwa-Sup
Department of Applied Biochemistry, Division of Life Science, College of Biomedical and Health Science, Konkuk University, Chungju, Korea.
Pharmacology. 2005 Dec;75(1):37-44. doi: 10.1159/000086192. Epub 2005 Jun 2.
The effects of a novel sodium/hydrogen exchanger-1 (NHE-1) inhibitor, KR-32568, were studied in an anesthetized rat model of 30 min ischemia/2.5 h reperfusion heart injury. KR-32568 dose-dependently inhibited NHE-1-mediated rabbit platelet swelling induced by intracellular acidification. In our anesthetized rat model, KR-32568 reduced infarct size from 67 (control) to 43 and 24% at 0.1 and 1.0 mg/kg (i.v. bolus, given 10 min before ischemia), respectively. KR-32568 at the same doses also significantly reduced the total number of ventricular premature beats during ischemia/reperfusion from 530 (control) to 266 and 115 beats, ventricular tachycardia (VT) incidence from 51 (control) to 21 and 8, VT duration from 238 s (control) to 63 and 33 s, ventricular fibrillation (VF) incidence from 17 (control) to 8 and 0, and VF duration from 85 s to 18 and 1 s. These results indicate that KR-32568 may exert potent cardioprotective effects in rats via inhibition of sodium/hydrogen exchanger-1.
在30分钟缺血/2.5小时再灌注心脏损伤的麻醉大鼠模型中,研究了新型钠/氢交换体-1(NHE-1)抑制剂KR-32568的作用。KR-32568呈剂量依赖性地抑制细胞内酸化诱导的NHE-1介导的兔血小板肿胀。在我们的麻醉大鼠模型中,KR-32568在0.1和1.0mg/kg(静脉推注,在缺血前10分钟给予)时,分别将梗死面积从67%(对照组)降至43%和24%。相同剂量的KR-32568还显著减少了缺血/再灌注期间室性早搏的总数,从530次(对照组)降至266次和115次,室性心动过速(VT)发生率从51%(对照组)降至21%和8%,VT持续时间从238秒(对照组)降至63秒和33秒,心室颤动(VF)发生率从17%(对照组)降至8%和0%,VF持续时间从85秒降至18秒和1秒。这些结果表明,KR-32568可能通过抑制钠/氢交换体-1在大鼠中发挥强大的心脏保护作用。