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作 者:任冰稳[1] 叶平[1] 刘永学[2] 高志清[2]
机构地区:[1]解放军总医院老年心血管二科,北京100853 [2]军事医学科学院放射医学研究所药理毒理室
出 处:《西南国防医药》2010年第1期10-12,共3页Medical Journal of National Defending Forces in Southwest China
摘 要:目的观察束缚应激对雄性Wistar大鼠心肌过氧化体增殖物激活型受体α(PPARα)、PPARβ和肌型肉碱棕榈酰转移酶-I(M-CPT-I)mRNA表达的影响。方法健康雄性Wistar大鼠,采用束缚应激模型,实验组大鼠每天给予束缚应激2次,每次3h。按照有无应激和应激时间长短分为正常对照组(C)、束缚1w(R1)、束缚2w(R2)和束缚4w组(R4)。采用逆转录酶多聚酶链反应(RT-PCR)检测各组心肌PPARα、PPARβ和M-CPT-I的mRNA表达水平。结果束缚应激1、2、4w大鼠心肌PPARαmRNA和M-CPT-I mRNA水平较正常对照组明显升高(P<0.01或P<0.05);心肌PPARβmRNA水平较正常对照组变化不明显(P>0.05)。结论束缚应激上调心肌PPARα和M-CPT-I mRNA表达,对PPARβ无明显影响,PPARα可能促进束缚应激大鼠脂肪酸氧化增加。Objective To explore the effects of restraint stress on the expressions of peroxisome proliferator - activated receptor - α ( PPARα ), peroxisome proliferator - activated receptor - β ( PPARβ ) and muscle carnitine palmitoyl transferase - I ( M - CPT - I) mRNA in the myocardium of rat. Methods According to the duration of restraint stress,healthy Wistar rats were divided into four groups : control group ( no restraint), R1 group ( 1 - week restraint), R2 group (2 -week restraint) and R4 group(4 - week restraint). In three experimental groups, animals were under restraint stress twice a day and 3 hours per stress. After the the restraint stress experiment ended,the expressions of PPARα,PPARβ and M - CPT - I mRNA in the myocardium were evaluated by reverse transcription polymerase chain reaction( RT - PCR). Results The expressions of myocardial PPARα mRNA and M - CPT - I mRNA in three groups under restraint stress were all significantly higher than those in control group ( P 〈 0.01 or P 〈 0.05 ), while the expression of PPARβ mRNA had no significant change compared with control group( P 〉 0.05 ). Conclusion Restraint stress can up - regulate the expressions of PPARα and M - CPT - I mRNA, but it had no effect on the expression of PPARβ mRNA. PPARoL may increase the myocardial fatty oxidation in rats under restraint stress. [
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