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The Effects of Soluble Epoxide Hydrolase Inhibition in Atherogenesis and Atherosclerotic Pro-gression
【机构】 北京大学医学部脂代谢与动脉粥样硬化研究室;
【摘要】 Epoxyeicosatrienoic acids(EETs),metabolites of arachidonic acid(AA),are known to have anti-inflammatory effects and hydrolyzed by soluble epoxide hydrolase(s EH).We aimed to investigate the effect of s EH inhibition on atherosclerotic progression.LDLR-/-mice with or without s EH inhibitor and LDLR and s EH double knockout(DK)mice were fed with western diet for 6 weeks to induce arteriosclerosis,and then half of the mice switched to chow diet supplemented with s EH inhibitor foranother 6 weeks.To further assess the role of s EH in atherosgenesis,we transplanted LDLR-/-or DK bone marrow into LDLR-/-recipients and also fed with 6 weeks western diet.The progression of atherosclerosis was evaluated and AA metabolites were analyzed by LC-MS/MS.The results revealed that s EH inhibition and gene knockout decreased western diet-induced high plasma LDL cholesterol level and the size of the atherosclerotic lesion in the aorta of the mice.Furthermore,mice with DK bone marrow transplantation developed less aortic lesion without diminished the cholesterol level in plasma.After diet switch,the cholesterol level dropped back to control level and the size of arotic lesion became smaller compared to the western diet group.When s EH inhibitor decreased s EH activity in the liver and increased EETs/DHETs ratio in the plasma,the plaque size seemed not being further reduced after diet switch.However,M2 type macrophage marker at protein and m RNA level was increased in the aortic lesions.In cultured macrophage,s EH inhibition and EETs supplements could increase the markers of M2macrophage at m RNA level.Thus,s EH inhibition and depletion in macrophage attenuated atherosclerosis when fed with western diet.Although the role of the s EH inhibitor on atherosclerosis progression and plaque stability need to be further investigated.EETs levels and s EH activity may play a pivotal role in atherogenesis and macrophage differentiation.
【Abstract】 Epoxyeicosatrienoic acids(EETs),metabolites of arachidonic acid(AA),are known to have anti-inflammatory effects and hydrolyzed by soluble epoxide hydrolase(s EH).We aimed to investigate the effect of s EH inhibition on atherosclerotic progression.LDLR-/-mice with or without s EH inhibitor and LDLR and s EH double knockout(DK) mice were fed with western diet for 6 weeks to induce arteriosclerosis,and then half of the mice switched to chow diet supplemented with s EH inhibitor foranother 6 weeks.To further assess the role of s EH in atherosgenesis,we transplanted LDLR-/-or DK bone marrow into LDLR-/-recipients and also fed with 6 weeks western diet.The progression of atherosclerosis was evaluated and AA metabolites were analyzed by LC-MS/MS.The results revealed that s EH inhibition and gene knockout decreased western diet-induced high plasma LDL cholesterol level and the size of the atherosclerotic lesion in the aorta of the mice.Furthermore,mice with DK bone marrow transplantation developed less aortic lesion without diminished the cholesterol level in plasma.After diet switch,the cholesterol level dropped back to control level and the size of arotic lesion became smaller compared to the western diet group.When s EH inhibitor decreased s EH activity in the liver and increased EETs/DHETs ratio in the plasma,the plaque size seemed not being further reduced after diet switch.However,M2 type macrophage marker at protein and m RNA level was increased in the aortic lesions.In cultured macrophage,s EH inhibition and EETs supplements could increase the markers of M2 macrophage at m RNA level.Thus,s EH inhibition and depletion in macrophage attenuated atherosclerosis when fed with western diet.Although the role of the s EH inhibitor on atherosclerosis progression and plaque stability need to be further investigated.EETs levels and s EH activity may play a pivotal role in atherogenesis and macrophage differentiation.
- 【会议录名称】 中国生理学会第24届全国会员代表大会暨生理学学术大会论文汇编
- 【会议名称】中国生理学会第24届全国会员代表大会暨生理学学术大会
- 【会议时间】2014-10-24
- 【会议地点】中国上海
- 【分类号】R543.5
- 【主办单位】中国生理学会