Pharmaceutical Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran.
Targeted Drug Delivery Research Center, Department of Pharmacodynamics and Toxicology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran.
Phytother Res. 2019 Mar;33(3):832-844. doi: 10.1002/ptr.6276. Epub 2019 Jan 17.
The mechanisms of bisphenol-A (BPA)-induced metabolic syndrome as well as the protective role of grape seed extract (GSE) and resveratrol were investigated. Rats were treated with BPA (0 and 35 mg·kg ·day , gavage) plus resveratrol (25, 50, and 100 mg·kg ·day , i.p.) or GSE (3, 6, 12 mg·kg ·day , i.p.) or vitamin E (200 IU/kg/every other day, i.p.). After 2 months, mean systolic blood pressure, serum lipid profile, glycaemia, and fat index were examined. By enzyme-linked immunosorbent assay, the serum concentrations of insulin, leptin, adiponectin, and paraoxonase 1, and by real-time polymerase chain reaction as well as western blotting, key liver elements in cholesterol hemostasis (LDLR, CYP7A1, ABCG5 and 8) and insulin signaling (p-Akt/Akt and p-PI3K/PI3K) were measured. BPA increased mean systolic blood pressure, total cholesterol, and low-density lipoprotein cholesterol and reduced paraoxonase1 and the hepatic expression of both ABCG5 and ABCG8. It increased the body fat index, leptin, adiponectin, insulin, and glycaemia level and decreased the hepatic protein expression of p-Akt/Akt and p-PI3K/PI3k. GSE, resveratrol, or vitamin E coadministration along with BPA restored the detrimental effects of BPA in some levels. Herein, the predisposing effects of BPA-induced metabolic syndrome were restored by GSE and resveratrol, linked to the regulation of insulin signaling, ABCG8 expression, and their antioxidant properties.
研究了双酚 A(BPA)诱导的代谢综合征的机制,以及葡萄籽提取物(GSE)和白藜芦醇的保护作用。大鼠用 BPA(0 和 35 mg·kg·day,灌胃)加白藜芦醇(25、50 和 100 mg·kg·day,腹腔注射)或 GSE(3、6、12 mg·kg·day,腹腔注射)或维生素 E(200 IU/kg/隔天,腹腔注射)治疗。2 个月后,检查平均收缩压、血清脂质谱、血糖和脂肪指数。通过酶联免疫吸附试验测定血清胰岛素、瘦素、脂联素和对氧磷酶 1 的浓度,通过实时聚合酶链反应和蛋白质印迹法测定胆固醇稳态(LDLR、CYP7A1、ABCG5 和 8)和胰岛素信号(p-Akt/Akt 和 p-PI3K/PI3K)的关键肝元素。BPA 增加平均收缩压、总胆固醇和低密度脂蛋白胆固醇,降低对氧磷酶 1 和 ABCG5 和 ABCG8 的肝表达。它增加了体脂肪指数、瘦素、脂联素、胰岛素和血糖水平,并降低了肝蛋白表达的 p-Akt/Akt 和 p-PI3K/PI3k。GSE、白藜芦醇或维生素 E 与 BPA 一起给药可在某些水平上恢复 BPA 的有害作用。在此,GSE 和白藜芦醇恢复了 BPA 诱导的代谢综合征的易患作用,与胰岛素信号、ABCG8 表达及其抗氧化特性的调节有关。