药理学_调血脂药和抗动脉粥样硬化药课件.ppt
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1、调血脂药和抗动脉粥样硬化药,Lipid-modulating drugs and Antiatherosclerotic drugs,Pathophysiology,损伤,血脂异常高血压吸烟,等,单核细胞,巨噬细胞,泡沫细胞,血管平滑肌细胞,脂质,Scavenger receptor,脂质,Atherosclerosis,Vascular endothelium modification in atherosclerosis,Plaque formation:The fatty streak,Pathophysiology,Atherosclerosis,泡沫细胞,脂质条纹,斑块前期,粥样斑块
2、,纤维粥样斑块,复合病变,十年,三十年,四十年,内皮功能障碍,From plaque to thrombosis,key event:plaque rupture,第一节 调血脂药,胆固醇(Ch)三酰甘油(TG)磷脂(PL)游离脂肪酸(FFA),血脂,脂蛋白,1.20,1.10,1.06,1.02,1.006,0.95,5,10,20,40,60,80,1000,Diameter(nm),Density(g/ml),Lipoprotein(Sub)Classes,高脂血症的分型,表型 血浆4 TC TG CM VLDL LDL 备注 过夜外观 I 奶油上层,下层清 易发胰腺炎IIa 透明 易发
3、冠心病IIb 透明 易发冠心病III 奶油上层 易发冠心病 下层混浊 IV 混浊 易发冠心病V 奶油上层 易发胰腺炎 下层混浊 注:示浓度升高;示浓度正常;示浓度降低,一.降低TC和LDL的药物二.降低TG及VLDL的药物三.降低Lp(a)的药物,(一)HMG-CoA还原酶抑制药 洛伐他汀;辛伐他汀 普伐他汀;氟伐他汀(二)胆汁酸结合树脂 考来烯胺,考来替泊(三)ACAT抑制药 甲亚油酰胺,(一)贝特类 吉非贝齐;非诺贝特(二)烟酸 烟酸;阿莫替司,Treatment of Hyperlipidemia,Expert Panel on Detection,Evaluation,and Trea
4、tment of High Blood Cholesterol in Adults.JAMA 2001;285:2486-2497.,High LDL-C,Therapeutic Lifestyle Change,Drug Therapy,Therapy of Choice:Statin,Alternative:Resin or niacin,Statins:Mechanism of Action,LDL receptormediated hepatic uptake of LDL and VLDL remnants,Serum VLDL remnants,Serum LDL-C,Choles
5、terol synthesis,LDL receptor(BE receptor)synthesis,Intracellular Cholesterol,Apo B,Apo E,Apo B,Systemic Circulation,Hepatocyte,Reduce hepatic cholesterol synthesis,lowering intracellular cholesterol,which stimulates upregulation of LDL receptor and increases the uptake of non-HDL particles from the
6、systemic circulation.,Serum IDL,VLDL,Potential Time Course of Statin Effects,*Time course established,Days,Years,LDL-C lowered*,Inflammationreduced,Vulnerableplaquesstabilized,Endothelialfunctionrestored,Ischemicepisodesreduced,Cardiaceventsreduced*,调血脂,改善血管内皮细胞功能,减轻炎性反应,减少缺血发作,稳定斑块,减少心血管事件,调血脂作用非调脂
7、作用 改善血管内皮;促进血管平滑肌细胞凋亡;稳定斑块;减轻血管炎性反应;抑制血小板聚集等,他汀类药理作用,他汀类临床应用,调血脂肾病综合征血管形成术后再狭窄预防心脑血管急性事件器官移植术后的排斥反应和骨质疏松症,Law MR et al.BMJ.2003;326:1423-1427.,*Standardized to LDL-C 186 mg/dL(mean concentration in trials)before treatment.Independent of pretreatment LDL-C.Maximum dose of 80 mg/d administered as two
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