Department of Nutrition and Exercise Physiology, Elson S. Floyd College of Medicine, Washington State University, 665 N Riverpoint Blvd, Spokane, WA 99210, USA.
Cells. 2020 Nov 20;9(11):2515. doi: 10.3390/cells9112515.
Obesity and type-2 diabetes trends continue to worsen in the United States. Dietary anthocyanins (typically provided by berries and other fruits) are reported to have protective effects against both conditions using a variety of experimental research models including animal and human feeding studies. This review highlights studies that explore the biochemical pathways in both tissue and rodent models which could explain clinical improvements noted with anthocyanin consumption. First, the primary mode of intestinal absorption of anthocyanins is through both sGLT1 and GLUT2 glucose transporters. Stronger binding affinities may allow anthocyanins to be more inhibitive to glucose absorption compared to the reverse, where GLUT2 expression may also be affected. Genetic or chemical inhibition of sGLT1 or GLUT2 demonstrate their essential function in anthocyanin absorption across the enterocyte, where the former interacts with a greater variety of anthocyanins but the latter is the major transporter for specific anthocyanin-glycosides. Once absorbed, anthocyanins positively modulate GLUT4 density and function in both skeletal muscle and adipose tissues via the upregulation of AMPK and restoration of insulin sensitivity. Antioxidant properties and phosphodiesterase inhibition by anthocyanins promote both mitochondrial function and density which could be novel targets for dietary management of obesity and its complications.
在美国,肥胖和 2 型糖尿病的趋势继续恶化。研究表明,膳食花色苷(通常来源于浆果和其他水果)对这两种疾病具有保护作用,其作用机制是通过多种实验研究模型,包括动物和人体喂养研究来实现的。本综述重点介绍了在组织和啮齿动物模型中探索花色苷代谢的生化途径的研究,这些途径可以解释花色苷摄入后临床改善的原因。首先,花色苷在肠道中的主要吸收方式是通过 SGLT1 和 GLUT2 葡萄糖转运蛋白。花色苷与葡萄糖转运蛋白的结合亲和力较强,可能会比 GLUT2 表达受影响时更能抑制葡萄糖的吸收。SGLT1 或 GLUT2 的遗传或化学抑制作用证明了它们在肠细胞吸收花色苷中的重要功能,前者与更多种类的花色苷相互作用,但后者是特定花色苷糖苷的主要转运蛋白。一旦被吸收,花色苷通过上调 AMPK 和恢复胰岛素敏感性,积极调节骨骼肌和脂肪组织中 GLUT4 的密度和功能。花色苷的抗氧化特性和磷酸二酯酶抑制作用促进了线粒体功能和密度的提高,这可能是肥胖及其并发症饮食管理的新靶点。