摘要
目的:探讨双环醇(bicyclol)对超氧阴离子(O2)诱导的血管舒张功能损伤的影响。方法:采用离体器官灌流技术,观察bicyclol对离体大鼠胸主动脉环张力的影响。采用焦酚(O2的供体)建立O2损伤模型,观察bicyclol预孵育对氧化应激损伤后血管内皮依赖性舒张功能的改善作用。结果:bicyclol(10-8~10-5mol/L)对由苯肾上腺素预收缩的内皮完整主动脉环产生舒张作用,该作用可被NO合酶抑制剂L-NAME和环氧化酶抑制剂吲哚美辛阻断。500μmol/L焦酚可引起乙酰胆碱诱导的主动脉环内皮依赖性舒张反应减弱,bicyclol(10-5mol/L)预孵育45 min可减轻焦酚的损伤作用。对于吲哚美辛处理的主动脉环,bicyclol(10-5mol/L)可抑制焦酚所致的血管舒张反应降低,但这一效应未见于L-NAME处理的主动脉环。结论:bicyclol具有内皮依赖性舒血管作用,并能对抗O2引起的血管舒张功能损伤,该作用通过NO途径介导。
Objective: To investigate the effect of bicyclol on vascular oxidative stress injury induced by superoxide anion.Methods: Rat thoracic aortic rings were isolated for isometric tension recording using organ bath technique.Superoxide arterial injury was induced by pyrogallol exposure,and the effect of bicyclol on endothelium-dependent relaxation was evaluated.Results: Bicyclol(10-8~10-5 mol/L) relaxed endothelium-intact aortic rings precontracted by phenylephrine.This effect was abolished by L-NAME,an inhibitor of nitric oxide synthase and indomethacin,an inhibitor of cyclooxygenase.Exposure to pyrogallol(500 μmol/L) resulted in decrease of acetylcholine(ACh)-induced endothelium-dependent relaxation in aortic rings,and pre-incubation of bicyclol(10-5 mol/L) for 45 min improved the relaxation attenuated by pyrogallol.In aortic rings pre-treated with indomethacin,bicyclol increased the ACh-induced relaxation that was inhibited by pyrogallol(500 μmol/L).This effect was not found in aortic rings pretreated with L-NAME.Conclusion: Bicyclol has endothelium-dependent vasodilating effect on rat thoracic aorta and improves vascular function by attenuating oxidative stress.Nitric oxide from endothelium is involved in the anti-oxidative effect of bicyclol.
出处
《中国应用生理学杂志》
CAS
CSCD
北大核心
2011年第1期81-85,共5页
Chinese Journal of Applied Physiology
关键词
双环醇
胸主动脉
氧化应激
内皮
舒张
bicyclol
thoracic aorta
oxidative stress
endothelium
relaxation