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菠萝叶对小鼠的降血脂机制:不同于贝特类药物,但类似于他汀类药物。

Hypolipidemic mechanisms of Ananas comosus L. leaves in mice: different from fibrates but similar to statins.

作者信息

Xie Weidong, Wang Wei, Su Hui, Xing Dongming, Cai Guoping, Du Lijun

机构信息

Laboratory of Life Sciences & Marine Biology, Life Sciences Division, Graduate School at Shenzhen, Tsinghua University, Shenzhen, China.

出版信息

J Pharmacol Sci. 2007 Mar;103(3):267-74. doi: 10.1254/jphs.fp0061244.

Abstract

In this study, we investigated hypolipidemic mechanisms of the ethanolic extract of Ananas comosus L. leaves (AC) in mice and then determined its activities in related enzymes. The results showed that AC (0.40 g/kg) significantly inhibited the increase in serum triglycerides by 40% in fructose-fed mice. In mice induced by alloxan and high-fat diets, serum total cholesterol remained at a high level (180 - 220 mg/dl) within 7 days of removing high-fat diets but reached normal level (120 - 140 mg/dl) after AC (0.40 g/kg per day) treatment. Also, AC (0.40 and 0.80 g/kg) significantly inhibited serum lipids from the increase in Triton WR-1339-induced hyperlipidemic mice. AC (0.01 - 100 microg/ml) selectively activated lipoprotein lipase (LPL) activity by 200% - 400% and significantly inhibited 3-hydroxyl-methyl glutaryl coenzyme A (HMGCoA) reductase activity by 20% - 49% in vitro. Furthermore, 2 months of fenofibrate (0.20 g/kg) administration particularly increased mice liver weights (0.0760 +/- 0.0110 g/g) while AC (0.40 g/kg) had no effect (0.0403 +/- 0.0047). Taken together, these results suggest that AC will be a new potential natural product for the treatment of hyperlipidemia that exerts its actions through mechanisms of inhibiting HMGCoA reductase and activating LPL activities. Its action mechanisms differentiate from those with fibrates but may be partly similar to those with statins. It is hopeful that AC may serve as the adjuvant for fibrates.

摘要

在本研究中,我们调查了菠萝叶乙醇提取物(AC)对小鼠的降血脂机制,然后测定了其对相关酶的活性。结果表明,AC(0.40 g/kg)显著抑制了果糖喂养小鼠血清甘油三酯40%的升高。在由四氧嘧啶和高脂饮食诱导的小鼠中,高脂饮食去除后7天内血清总胆固醇保持在高水平(180 - 220 mg/dl),但在AC(0.40 g/kg/天)治疗后达到正常水平(120 - 140 mg/dl)。此外,AC(0.40和0.80 g/kg)显著抑制了Triton WR - 1339诱导的高脂血症小鼠血清脂质的升高。AC(0.01 - 100 μg/ml)在体外选择性激活脂蛋白脂肪酶(LPL)活性200% - 400%,并显著抑制3 - 羟基 - 3 - 甲基戊二酰辅酶A(HMGCoA)还原酶活性20% - 49%。此外,非诺贝特(0.20 g/kg)给药2个月特别增加了小鼠肝脏重量(0.0760 +/- 0.0110 g/g),而AC(0.40 g/kg)则无影响(0.0403 +/- 0.0047)。综上所述,这些结果表明,AC将是一种治疗高脂血症的新的潜在天然产物,其通过抑制HMGCoA还原酶和激活LPL活性的机制发挥作用。其作用机制与贝特类药物不同,但可能部分类似于他汀类药物。有望AC可作为贝特类药物的辅助药物。

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