Xu Y C, Yeung D K Y, Man R Y K, Leung S W S
Department of Pharmacology, Faculty of Medicine, The University of Hong Kong, Hong Kong, SAR, China.
Mol Cell Biochem. 2006 Jul;287(1-2):61-7. doi: 10.1007/s11010-005-9061-y. Epub 2006 May 12.
The vascular effects of kaempferol were investigated in isolated porcine coronary artery rings. U46619 (9,11-dideoxy-9alpha, 11alpha-methanoepoxy prostaglandin F2alpha, 30 nM) was used to contract porcine coronary arterial rings. Concentration relaxation curve of kaempferol (1 nM - 100 microM) was constructed and kaempferol demonstrated significant relaxation at high concentrations. At low concentration with no significant effect on relaxation, kaempferol (10 microM) enhanced relaxation produced by bradykinin, the calcium ionophore A23187, isoproterenol and sodium nitroprusside in endothelium-intact porcine coronary arteries. In endothelium-disrupt rings, kaempferol (10 microM) also enhanced the relaxation caused by isoproterenol, sodium nitroprusside, levcromakalim and nifedipine. On the other hand, antioxidant agents did not affect bradykinin-induced relaxation or the enhancement effect of kaempferol. In summary, a low concentration of kaempferol (10 microM), devoid of significant vascular effect, has the ability to enhance endothelium-dependent and endothelium-independent relaxations. This action of kaempferol is unrelated to its antioxidant property.
在离体猪冠状动脉环中研究了山奈酚的血管效应。使用U46619(9,11-二脱氧-9α,11α-甲撑环氧前列腺素F2α,30 nM)使猪冠状动脉环收缩。构建了山奈酚(1 nM - 100 μM)的浓度-舒张曲线,山奈酚在高浓度时表现出显著的舒张作用。在低浓度时对舒张无显著影响,山奈酚(10 μM)增强了缓激肽、钙离子载体A23187、异丙肾上腺素和硝普钠在完整内皮猪冠状动脉中产生的舒张作用。在去内皮环中,山奈酚(10 μM)也增强了异丙肾上腺素、硝普钠、左旋克罗卡林和硝苯地平引起的舒张作用。另一方面,抗氧化剂不影响缓激肽诱导的舒张或山奈酚的增强作用。总之,低浓度的山奈酚(10 μM)无显著血管效应,但具有增强内皮依赖性和非内皮依赖性舒张的能力。山奈酚的这一作用与其抗氧化特性无关。