Protective effects of nicaraven, a new hydroxyl radical scavenger, on the endothelial dysfunction after exposure of pig coronary artery to hydroxyl radicals
Protective effects of nicaraven, a new hydroxyl radical scavenger, on the endothelial dysfunction after exposure of pig coronary artery to hydroxyl radicals
复制标题
新型羟自由基清除剂尼卡芬对猪冠状动脉羟自由基暴露后内皮功能障碍的保护作用
DOI:
--
复制
发表时间:
2004
影响因子:
4.3
通讯作者:
K. Tamura
中科院分区:
文献类型:
--
作者:
Mohammed Shah Alam;K. Ku;M. Yamauchi;M. Hashimoto;S. Nosaka;M. S. Hossain;S. Masumura;K. Nakayama;K. Tamura
Recently, we have reported that a new synthetic compound, 1,2bis(nicotinamido)-propane (nicaraven), improved cardiac function following preservation and reperfusion. In this study, we investigated the efficacy of nicaraven as a radical scavenger by using an in vitro model of oxidative stress, to clarify mechanisms of the protective effect of this new compound on reperfusion injury in rat heart. Ring segments of epicardial right coronary arteries (RCA) of pig were suspended in organ chambers and exposed to hydroxyl radicals (·OH), generated (by two different systems ) by 0.28 mM FeSO4/0.28 mM H2O2 and DHF/Fe3+-ADP (2.4 mM, 43 nM, and 1.56 uM, respectively) to the bathing solution for 60 min. Prior exposure of the coronary arteries to ·OH significantly produced right-ward shift of the dose-response curves of the bradykinin-induced endothelium-dependent relaxations (an increase in the ED50 value for bradykinin by 4.37 and 1.98 times than control in two different ·OH generating systems, respectively), but did not affect the maximum relaxation responses. The presence of nicaraven (10-4 and 10-5 M) in the ·OH generating system, shifted the dose-response curves to bradykinin to the control level, suggesting a significant hydroxyl radical scavenging effect of the drug. These results indicate that nicaraven, a new hydroxyl radical scavenger, exhibits a protective effect on hydroxyl radicalinduced endothelial dysfunctions of pig coronary artery.
DOI:
10.1152/ajpheart.1993.265.1.h299
发表时间:
1993
期刊:
The American journal of physiology
影响因子:
--
作者:
Hashimoto,M;Close,LA;Ishida,Y;Paul,RJ
通讯作者:
Paul,RJ
影响因子:
37.8
作者:
Pearson,PJ;Schaff,HV;Vanhoutte,PM
通讯作者:
Vanhoutte,PM
DOI:
10.1073/pnas.85.11.4046
发表时间:
1988-06-01
影响因子:
11.1
作者:
ZWEIER, JL;KUPPUSAMY, P;LUTTY, GA
通讯作者:
LUTTY, GA