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机构地区:[1]天津体育学院运动医学研究所,天津300381
出 处:《中国运动医学杂志》2001年第3期232-235,255,共5页Chinese Journal of Sports Medicine
基 金:天津市自然科学基金资助(项目号983608011;003606211)
摘 要:目的:以RT-PCR技术测定和分析高脂高胆固醇膳食和有氧运动干预对高胆固醇血症大鼠肝脏卵磷脂胆固醇酯酰转移酶(LCAT)和载脂蛋白 AI(apoAI)基因表达的影响,探讨有氧运动对胆固醇逆向转运(RCT)通路影响的分子机理。方法:雄性SD大鼠40只,随机分为:1)8周普通膳食对照组(NS,n=10),2) 8周高脂膳食对照组(HS,n=10),3)8周普通膳食+运动组(NE,n=10)和4)8周高脂膳食+运动组(HE,n=10)。建立高脂高胆固醇膳食诱导SD大鼠高脂血症的实验动物模型和有氧运动训练模型,用 RT-PCR方法测定肝脏LCAT mRNA和apoAI mRNA表达量。结果:(1)NE组大鼠肝脏LCAT mRNA的表达较NS组显著增高(P<0.05);(2)HS组LCAT和apoAI mRNA表达较NS组均显著降低(P<0.01);(3)HE组LCAT和apoAI mRNA较 HS组显著升高(P<0.01),且 LCAT mRNA与 NS组相比无显著差异,但是apoAI mRNA的表达仍显著低于NS组(P<0.01);(4)肝脏apoAI mRNA的表达量与血清HDL-C的水平无显著相关;在NE、HS和HE组中肝?Objective: In order to explore the molecular mechanism of the effect of exercise on reverse cholesterol transport (RCT, we observed the effect of exercise on hepatic expression of lecithin cholesterol acyltransferase (LCAT) and apoAI mRNA by RT-PCR. Methods: SD rats were divided into four groups: 1) normal diet for 8 weeks (NS); 2) high -fat-high-cholesterol (HFC) diet for 8weeks (HS); 3) normal diet and aerobic exercise for 8weeks(NE); 4) HFC diet and aerobic exercise for 8weeks. Our study used RT-PCR determining the effect of aerobic swimming exercise on hepatic levels Of LCAT and apoA I mRNA in hyperlipidemic rats. Results: The hepatic levels of LCAT mRNA in NE group are higher than NS group (P<0.05); The LCAT and apoAI mRNA in HS group are lower than NS group (P<0.01); The hepatic mRNA levels of LCAT and apoAI of HE group were higher than HS group (P<0.01). At the same time, it was discovered that there was relationship between the expression of hepatic LCAT mRNA in NE, HS and HE group. Conclusions: HFC diet can down-regulate the hepatic transcription of LCAT and apoAI gene in rats. Swimming training might protect against the atherogenic effects of HFC diet by up-regulate the hepatic transcription of LCAT and apoAI gene, and the expression of LCAT are closely related with the serum levels of HDL-C during the exercise treatment. Thus, these molecular regulating might be responsible for the availability of reverse cholesterol transport in hyperlipidemia.
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