Jiangxi Provincial Key Laboratory of Drug Design and Evaluation, Jiangxi Key Laboratory of Organic Chemistry, Jiangxi Science and Technology Normal University, No. 605, Fenglin Road, Jingkai District, Nanchang 330013, P.R. China.
Exp Anim. 2023 Feb 21;72(1):123-131. doi: 10.1538/expanim.22-0115. Epub 2022 Oct 31.
A comparative study was conducted to determine whether hesperetin and pectolinarigenin could lower total cholesterol (TC), triglycerides (TG), low-density lipoprotein cholesterol (LDL), and high-density lipoprotein cholesterol (HDL) in a high-fat diet (HFD)-induced high lipid model in Golden Syrian hamsters. 48 Golden Syrian hamsters (8 weeks old) were fed with a HFD for 15 days. HFD induced significant increases in plasma TC, TG, LDL, and HDL. Then, these high lipid hamsters were divided into four groups and were administered with 0.5% sodium carboxymethyl cellulose (CMC-Na), hesperetin (100 mg/kg/day), pectolinarigenin (100 mg/kg/day) or atorvastatin (1.0 mg/kg/day), for 7 weeks. It was found that pectolinarigenin treatment resulted in significant reductions in body weight, adiposity index, serum levels of TC, TG and hepatic TC, TG and free fatty acid compared to those in control hamsters with hyperlipidemia (P<0.05). However, hesperetin treatment only caused reductions in plasma TC and hepatic TG levels. Besides, the hamsters treated with pectolinarigenin showed a relatively normal hepatic architecture compared to the hepatic steatosis shown in the control group. Moreover, the expressions of fatty-acid synthase (Fasn) and solute carrier family 27 member 1 (Slc27a1) involved in lipid biosynthesis, were suppressed in the pectolinarigenin-treated groups, and the expression of carnitine palmitoyltransferase 1A (Cpt1a) involved in fatty acid oxidation was increased in the pectolinarigenin-treated group. Taken together, these results suggest pectolinarigenin exerts stronger protective effects against hyperlipidemia and hepatic steatosis than hesperetin, which may involve the inhibition of lipid uptake and biosynthesis.
一项对比研究旨在探究橙皮素和川陈皮素是否能降低高脂肪饮食(HFD)诱导的高脂模型中金黄地鼠的总胆固醇(TC)、甘油三酯(TG)、低密度脂蛋白胆固醇(LDL)和高密度脂蛋白胆固醇(HDL)。48 只 8 周龄金黄地鼠喂食 HFD 15 天,HFD 诱导的血浆 TC、TG、LDL 和 HDL 显著增加。然后,将这些高脂血症金黄地鼠分为四组,分别给予 0.5%羧甲基纤维素钠(CMC-Na)、橙皮素(100mg/kg/天)、川陈皮素(100mg/kg/天)或阿托伐他汀(1.0mg/kg/天),治疗 7 周。结果表明,与高脂血症对照组相比,川陈皮素治疗组体重、肥胖指数、血清 TC、TG 和肝 TC、TG 和游离脂肪酸显著降低(P<0.05)。然而,橙皮素治疗仅导致血浆 TC 和肝 TG 水平降低。此外,川陈皮素治疗组的肝脏结构相对正常,而对照组则显示出肝脂肪变性。此外,参与脂质生物合成的脂肪酸合成酶(Fasn)和溶质载体家族 27 成员 1(Slc27a1)的表达在川陈皮素治疗组中受到抑制,而参与脂肪酸氧化的肉碱棕榈酰转移酶 1A(Cpt1a)的表达在川陈皮素治疗组中增加。综上所述,这些结果表明川陈皮素对高脂血症和肝脂肪变性的保护作用强于橙皮素,这可能涉及脂质摄取和生物合成的抑制。