In vivo Evaluation of Berberine-loaded Liposomes in the Exogenous Hyperlipidemia Animal Model

Duong Thi Thuan, Nguyen Thi Quynh Trang, Nguyen Thuy Duong, Nguyen Thi Thanh Hai, Pham Thi Minh Hue
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Abstract

Berberine (BBR) is an alkaloid presenting exogenous cholesterol lowering and anti-hyperlipidemia therapeutic effects in the literature. In this study, the exogenous lipid-lowering effects of oral BBR-loaded liposomes were investigated in rats compared with free BBR within four weeks. The BBR-loaded liposomes at the daily oral dose of 25 mg BBR/kg of body weight in rats reduced total cholesterol (TC) and low-density lipoprotein cholesterol (LDL-C) by 22.34% (p>0.05), 43.93% (p<0.05), respectively. These values (TC and LDL-C) when rats were given BBR-loaded liposomes at the daily oral dose of 50 mg BBR/kg were 30.72% (p<0.05) and 42.77% (p<0.05) compared with those values of the untreated control group, respectively. Both doses of BBR-loaded liposomes have no signals in decreasing triglycerides. Keywords: Berberine, berberine-loaded liposomes, anti-hyperlipidemia, animal model.
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小檗碱脂质体在外源性高脂血症动物模型中的体内评估
小檗碱(BBR)是一种生物碱,在文献中具有外源性降低胆固醇和抗高脂血症的疗效。本研究对大鼠口服小檗碱脂质体与游离小檗碱脂质体在四周内的外源性降脂效果进行了比较。大鼠每天口服 25 毫克 BBR/千克体重的 BBR 脂质体后,总胆固醇(TC)和低密度脂蛋白胆固醇(LDL-C)分别降低了 22.34%(p>0.05)和 43.93%(p<0.05)。当大鼠每天口服 50 毫克 BBR/kg 剂量的 BBR 脂质体时,这些值(TC 和 LDL-C)与未处理的对照组相比分别降低了 30.72% (p<0.05) 和 42.77% (p<0.05)。两种剂量的BBR脂质体都没有降低甘油三酯的信号。 关键词小檗碱 小檗碱脂质体 抗高脂血症 动物模型
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