Renal Physiology Unit, Department of Physiology, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.
Nutrition and Exercise Unit, Department of Physiology, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.
Biomolecules. 2021 Aug 17;11(8):1224. doi: 10.3390/biom11081224.
Diabetic nephropathy (DN) is the primary cause of end-stage renal disease worldwide. Oxidative stress and mitochondrial dysfunction are central to its pathogenesis. Rice husk, the leftover from the milling process, is a good source of phytochemicals with antioxidant activity. This study evaluated the possible protection of purple rice husk extract (PRHE) against diabetic kidney injury. Type 2 diabetic rats were given vehicle, PRHE, metformin, and PRHE+metformin, respectively, while nondiabetic rats received vehicle. After 12 weeks, diabetic rats developed nephropathy as proven by metabolic alterations (increased blood glucose, insulin, HOMA-IR, triglycerides, cholesterol) and renal abnormalities (podocyte injury, microalbuminuria, increased serum creatinine, decreased creatinine clearance). Treatment with PRHE, metformin, or combination diminished these changes, improved mitochondrial function (decreased mitochondrial swelling, reactive oxygen species production, membrane potential changes), and reduced renal oxidative damage (decreased lipid peroxidation and increased antioxidants). Increased expression of PGC-1α, SIRT3, and SOD2 and decreased expression of Ac-SOD2 correlated with the beneficial outcomes. HPLC revealed protocatechuic acid and cyanidin-3-glucoside as the key components of PRHE. The findings indicate that PRHE effectively protects against the development of DN by retaining mitochondrial redox equilibrium via the regulation of PGC-1α-SIRT3-SOD2 signaling. This study creates an opportunity to develop this agricultural waste into a useful health product for diabetes.
糖尿病肾病(DN)是全球终末期肾病的主要原因。氧化应激和线粒体功能障碍是其发病机制的核心。稻壳是碾米过程中的剩余物,是具有抗氧化活性的植物化学物质的良好来源。本研究评估了紫稻壳提取物(PRHE)对糖尿病肾病损伤的可能保护作用。2 型糖尿病大鼠分别给予载体、PRHE、二甲双胍和 PRHE+二甲双胍,而非糖尿病大鼠给予载体。12 周后,糖尿病大鼠发生了肾病,代谢改变(血糖、胰岛素、HOMA-IR、甘油三酯、胆固醇升高)和肾脏异常(足细胞损伤、微量白蛋白尿、血清肌酐升高、肌酐清除率降低)证明了这一点。PRHE、二甲双胍或联合治疗可减轻这些变化,改善线粒体功能(减少线粒体肿胀、活性氧产生、膜电位变化),减少肾脏氧化损伤(减少脂质过氧化和增加抗氧化剂)。PGC-1α、SIRT3 和 SOD2 的表达增加,Ac-SOD2 的表达减少与有益结果相关。HPLC 显示原儿茶酸和矢车菊素-3-葡萄糖苷是 PRHE 的关键成分。研究结果表明,PRHE 通过调节 PGC-1α-SIRT3-SOD2 信号通路,有效保护糖尿病大鼠免受 DN 的发展,维持线粒体氧化还原平衡。这项研究为开发这种农业废物成为糖尿病的有用保健品创造了机会。