Guangdong Provincial Key Laboratory of Food, Nutrition and Health, Department of Nutrition, School of Public Health, Sun Yat-sen University, Guangzhou 510080, China.
Guangzhou Key Laboratory of Environmental Pollution and Health Risk Assessment, Department of Occupational and Environmental Health, School of Public Health, Sun Yat-sen University, Guangzhou 510080, China.
Nutrients. 2022 Apr 27;14(9):1828. doi: 10.3390/nu14091828.
Curcumin is a polyphenol that has been shown to have prebiotic and cholesterol-lowering properties. This study aimed to investigate the impact of curcumin on bile cholesterol supersaturation and the potential mechanistic role of intestinal microbiota and cholesterol absorption. Male hamsters (n = 8) were fed a high-fat diet (HFD) supplemented with or without curcumin for 12 weeks. Results showed that curcumin significantly decreased cholesterol levels in the serum (from 5.10 to 4.10 mmol/L) and liver (from 64.60 to 47.72 nmol/mg protein) in HFD-fed hamsters and reduced the bile cholesterol saturation index (CSI) from 1.64 to 1.08 due to the beneficial modifications in the concentration of total bile acids (BAs), phospholipids and cholesterol (p < 0.05). Gut microbiota analysis via 16S rRNA sequencing revealed that curcumin modulated gut microbiota, predominantly increasing microbiota associated with BA metabolism and short-chain fatty acid production, which subsequently up-regulated the expression of hepatic cholesterol 7-alpha hydroxylase and increased the synthesis of bile acids (p < 0.05). Furthermore, curcumin significantly down-regulated the expression of intestinal Niemann−Pick C1-like protein 1(NPC1L1) in hamsters and reduced cholesterol absorption in Caco-2 cells (p < 0.05). Our results demonstrate that dietary curcumin has the potential to prevent bile cholesterol supersaturation through modulating the gut microbiota and inhibiting intestinal cholesterol absorption.
姜黄素是一种多酚,已被证明具有益生元和降低胆固醇的特性。本研究旨在探讨姜黄素对胆汁胆固醇过饱和度的影响,以及肠道微生物群和胆固醇吸收的潜在机制作用。雄性仓鼠(n = 8)喂食高脂肪饮食(HFD),并补充或不补充姜黄素,共 12 周。结果表明,姜黄素可显著降低 HFD 喂养仓鼠血清(从 5.10 降至 4.10mmol/L)和肝脏(从 64.60 降至 47.72nmol/mg 蛋白)中的胆固醇水平,并降低胆汁胆固醇饱和度指数(CSI),从 1.64 降至 1.08,这归因于总胆汁酸(BAs)、磷脂和胆固醇浓度的有益变化(p < 0.05)。通过 16S rRNA 测序进行的肠道微生物组分析表明,姜黄素调节了肠道微生物群,主要增加了与 BA 代谢和短链脂肪酸生成相关的微生物群,进而上调了肝脏胆固醇 7-α羟化酶的表达,增加了胆汁酸的合成(p < 0.05)。此外,姜黄素可显著下调仓鼠肠道 Niemann−Pick C1 样蛋白 1(NPC1L1)的表达,并降低 Caco-2 细胞中的胆固醇吸收(p < 0.05)。我们的研究结果表明,膳食姜黄素通过调节肠道微生物群和抑制肠道胆固醇吸收,具有预防胆汁胆固醇过饱和度的潜力。