机构地区:[1]潍坊医学院基础医学院,山东省潍坊261053 [2]山东大学医学院 [3]潍坊医学院公共卫生学院 [4]潍坊医学院临床学院
出 处:《中国慢性病预防与控制》2013年第1期12-14,共3页Chinese Journal of Prevention and Control of Chronic Diseases
基 金:山东省科技厅资助课题(2006GG2302015);山东省中医药管理局资助课题(2005236)
摘 要:目的探讨马齿苋脂肪油有效成分对肝脏卵磷脂胆固醇酯酰转移酶(LCAT)、载脂蛋白AI(apoAI)和高密度脂蛋白受体(SR-BI)基因表达的干预作用,分析马齿苋调节胆固醇逆向转运(RCT)通路的分子机制。方法健康雄性SD大鼠24只,随机分为模型组、多烯康组、马齿苋组、正常组,每组6只。应用高脂高胆固醇膳食诱导建立动脉粥样硬化(AS)大鼠模型,用定量反转录聚合酶链式反应(RT-PCR)技术测定LCAT、apoAI及SR-BI mRNA表达量,以免疫比浊法、沉淀法测定血清apoAI、高密度脂蛋白胆固醇(HDL-C)含量。结果模型组大鼠肝脏LCAT mRNA和apoAI mRNA的表达量明显下降,分别为0.43±0.20、2.33±0.35,与正常组(分别为1.49±0.32、6.30±0.82)、多烯康组(分别为1.15±0.16、4.32±0.69)、马齿苋组(分别为1.12±0.12、4.21±0.76)比较,差异均有统计学意义(P<0.05)。模型组大鼠血清apoAI([0.15±0.03)g/L]和HDL-C水平([0.53±0.25)mmol/L]明显下降,与马齿苋组([0.39±0.09)g/L、(0.86±0.04)mmol/L]比较,差异有统计学意义(P<0.05)。除正常组外,多烯康组、马齿苋组、模型组肝脏LCAT mRNA表达量与HDL-C水平均呈明显的正相关(r值分别为0.935、0.927、0.892,P<0.01)。模型组大鼠肝脏SR-BI mRNA水平(1.33±0.57)下降,马齿苋组(3.20±0.41)高于模型组,差异有统计学意义(P<0.01)。结论在转录水平阻抗高脂高胆固醇负荷下调大鼠肝脏LCAT和apoAI mRNA以及SR-BI mRNA表达的作用,促进RCT过程是马齿苋改善高脂血症、抗动脉粥样硬化的重要分子机制。Objective To explore the effects of portulaca oleracea fatty oil active ingredients on hepatic lecithin cholesterol acyl transferase (LCAT), apolipoproteinAI (apoAI) and high density lipoprotein receptor(SR-BI) gene expression and to analyze the molecular mechanism of regulating reverse cholesterol transportation(RCT) pathway by purslane. Methods Twenty four healthy male SD rats were randomly divided into four groups: model group, duoxikang group, portulaca group and the control group (6 rats each group). Animal model of atherosclerosis (AS) was prepared with high-fat and high-cholesterol diet. RT-PCR was used to detect the expression levels of hepatic LCAT, apoAI and SR-BI mRNA. The serum apoAI and HDL-C levels were measured with immune turbidimetry and precipitation methods. Results The expression levels of hepatic LCAT mRNA and apoAI mRNA in model group were 0.43±0.20 and 2.33±0.35 respectively, which were significantly lower than those ( 1.49±0.32 and 6.30±0.82) in control group, those (1.15±0.16 and 4.32±0.69) in duoxikang group and those ( 1.12±0.12 and 4.21±0.76) in portulaca group (P〈0.05). The serum apoAI and HDL-C levels in model group were (0.15±0.03) g/L and (0.53±0.25) mmol/L respectively, which were significantly lower than those [(0.39±0.09) g/L and (0.86±0.04) retool/L] in portulaca group (P〈0.05). There were positive correlation between hepatic expression levels and serum HDL-C levels in duoxikang group, portulaca group and model group (r=0.935, 0.927 and 0.892,P〈0.01 ). The hepatic SR-BI mRNA expression level (1.33±0.57) in model group was obviously lower than that (3.20±0.41) in portulaca group (P〈0.05). Conclusion The molecular mechanisms of purslane anti-AS effects may be due to own-regulating hepatic LCAT, apoAI and SR-BI mRNA expression and improving RCT.
关 键 词:动脉粥样硬化 马齿苋 载脂蛋白 基因表达 卵磷脂胆固醇酯酰转移酶 高密度脂蛋白受体 胆固醇逆向转运
分 类 号:R543.5[医药卫生—心血管疾病]
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