Cardioprotective Effect of Licochalcone D against Myocardial Ischemia/Reperfusion Injury in Langendorff-Perfused Rat Hearts.
Cardioprotective Effect of Licochalcone D against Myocardial Ischemia/Reperfusion Injury in Langendorff-Perfused Rat Hearts.
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DOI:
10.1371/journal.pone.0128375
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发表时间:
2015
期刊:
影响因子:
3.7
通讯作者:
Li CG
中科院分区:
文献类型:
--
作者:
Yuan X;Niu HT;Wang PL;Lu J;Zhao H;Liu SH;Zheng QS;Li CG
Flavonoids are important components of ‘functional foods’, with beneficial effects on cardiovascular function. The present study was designed to investigate whether licochalcone D (LD) could be a cardioprotective agent in ischemia/reperfusion (I/R) injury and to shed light on its possible mechanism. Compared with the I/R group, LD treatment enhanced myocardial function (increased LVDP, dp/dt max, dp/dt min, HR and CR) and suppressed cardiac injury (decreased LDH, CK and myocardial infarct size). Moreover, LD treatment reversed the I/R-induced cleavage of caspase-3 and PARP, resulting in a significant decrease in proinflammatory factors and an increase in antioxidant capacity in I/R myocardial tissue. The mechanisms underlying the antiapoptosis, antiinflammation and antioxidant effects were related to the activation of the AKT pathway and to the blockage of the NF-κB/p65 and p38 MAPK pathways in the I/R-injured heart. Additionally, LD treatment markedly activated endothelial nitric oxide synthase (eNOS) and reduced nitric oxide (NO) production. The findings indicated that LD had real cardioprotective potential and provided support for the use of LD in myocardial I/R injury.
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DOI:
10.1016/0306-3623(93)90159-u
发表时间:
1993-07-01
期刊:
GENERAL PHARMACOLOGY-THE VASCULAR SYSTEM
影响因子:
--
作者:
DUARTE, J;VIZCAINO, FP;ZARZUELO, A
通讯作者:
ZARZUELO, A
DOI:
10.1161/01.atv.17.11.2744
发表时间:
1997-11-01
影响因子:
8.7
作者:
Hayek, T;Fuhrman, B;Aviram, M
通讯作者:
Aviram, M
影响因子:
3.1
作者:
Fang, Fang;Li, Dongye;Sun, Hong
通讯作者:
Sun, Hong
DOI:
10.1152/ajpheart.01072.2005
发表时间:
2006-05-01
影响因子:
4.8
作者:
Khan, M;Varadharaj, S;Kuppusamy, P
通讯作者:
Kuppusamy, P
影响因子:
20.1
作者:
Bowden, RA;Ding, ZM;Burns, AR
通讯作者:
Burns, AR