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红参酸性多糖的降脂作用。

Anti-hyperlipidemic effects of red ginseng acidic polysaccharide from Korean red ginseng.

机构信息

Korea Ginseng Corporation Central Research Institute, Daejon 305-805, Korea.

出版信息

Biol Pharm Bull. 2010;33(3):468-72. doi: 10.1248/bpb.33.468.

Abstract

It has been reported that red ginseng acidic polysaccharide (RGAP), isolated from Korean red ginseng, displays immunostimulatory and anti-tumor activities. In a follow-up study, we have carried out a study on the anti-hyperlipidemic effects of RGAP using hyperlipidemic rats acutely induced by Triton WR1339 or corn oil intravenously injected. Oral administration of RGAP (100 to 1000 mg/kg) dose-dependently reduced the serum levels of triglyceride (TG) up-regulated by Triton WR1339, an inducer of endogenous model hyperlipidemia. Moreover, RGAP treatment was shown to significantly decrease the levels of non-esterified fatty acid (NEFA) concomitant with TG reduction. However, such reduction effects were not observed in cases of total cholesterol (TC) and phospholipid levels increased under the same conditions, although there was an inhibitory tendency. Similar suppressive patterns were also seen in hepatic parameters (total lipids and TG) under the same conditions. The exogenous hyperlipidemic rat condition triggered by corn oil also supported the anti-hyperlipidemic activity of RGAP in serum and hepatic parameters of TG and NEFA. Interestingly, RGAP significantly enhanced the serum activity of lipoprotein lipase, a key hydrolytic enzyme of lipid molecules in lipoprotein, in a dose-dependent manner up to 80%, implying potential involvement of this enzyme in lowering TG and NEFA by RGAP. Therefore, our data suggest that RGAP may play an additional role in reducing hyperlipidemic conditions, which can be used as a valuable neutraceutical application for the treatment of hyperlipidemia.

摘要

据报道,从韩国红参中分离得到的红参酸性多糖(RGAP)具有免疫刺激和抗肿瘤活性。在后续研究中,我们使用静脉注射 Triton WR1339 或玉米油急性诱导的高脂血症大鼠研究了 RGAP 的抗高脂血症作用。RGAP(100 至 1000mg/kg)口服给药可剂量依赖性降低 Triton WR1339 上调的血清甘油三酯(TG)水平,Triton WR1339 是内源性模型高脂血症的诱导剂。此外,RGAP 治疗可显著降低与 TG 降低同时发生的非酯化脂肪酸(NEFA)水平。然而,在相同条件下,TC 和磷脂水平升高的情况下,并未观察到这种降低作用,尽管存在抑制趋势。在相同条件下,肝参数(总脂质和 TG)也表现出类似的抑制模式。玉米油引发的外源性高脂血症大鼠模型也支持 RGAP 在血清和肝参数 TG 和 NEFA 中的抗高脂血症活性。有趣的是,RGAP 可显著增强脂蛋白脂肪酶的血清活性,脂蛋白脂肪酶是脂蛋白中脂质分子的关键水解酶,高达 80%,这表明该酶可能参与了 RGAP 降低 TG 和 NEFA 的作用。因此,我们的数据表明,RGAP 可能在降低高脂血症方面发挥额外作用,可作为治疗高脂血症的有价值的营养保健品应用。

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