Effects of Resveratrol on the Renin-Angiotensin System in the Aging Kidney.
In-Ae JangEun Nim KimJi Hee LimMin Young KimTae Hyun BanHye Eun YoonCheol Whee ParkYoon Sik ChangBum Soon ChoiPublished in: Nutrients (2018)
The renin-angiotensin system (RAS), especially the angiotensin II (Ang II)/angiotensin II type 1 receptor (AT1R) axis, plays an important role in the aging process of the kidney, through increased tissue reactive oxygen species production and progressively increased oxidative stress. In contrast, the angiotensin 1-7 (Ang 1-7)/Mas receptor (MasR) axis, which counteracts the effects of Ang II, is protective for end-organ damage. To evaluate the ability of resveratrol (RSV) to modulate the RAS in aging kidneys, eighteen-month-old male C57BL/6 mice were divided into two groups that received either normal mouse chow or chow containing resveratrol, for six months. Renal expressions of RAS components, as well as pro- and antioxidant enzymes, were measured and mouse kidneys were isolated for histopathology. Resveratrol-treated mice demonstrated better renal function and reduced albuminuria, with improved renal histologic findings. Resveratrol suppressed the Ang II/AT1R axis and enhanced the AT2R/Ang 1-7/MasR axis. Additionally, the expression of nicotinamide adenine dinucleotide phosphate oxidase 4, 8-hydroxy-2'-deoxyguanosine, 3-nitrotyrosine, collagen IV, and fibronectin was decreased, while the expression of endothelial nitric oxide synthase and superoxide dismutase 2 was increased by resveratrol treatment. These findings demonstrate that resveratrol exerts protective effects on aging kidneys by reducing oxidative stress, inflammation, and fibrosis, through Ang II suppression and MasR activation.
Keyphrases
- angiotensin ii
- oxidative stress
- angiotensin converting enzyme
- vascular smooth muscle cells
- wild type
- poor prognosis
- nitric oxide synthase
- reactive oxygen species
- dna damage
- binding protein
- nitric oxide
- diabetic rats
- endothelial cells
- anti inflammatory
- type diabetes
- hydrogen peroxide
- induced apoptosis
- adipose tissue
- metabolic syndrome
- endoplasmic reticulum stress
- newly diagnosed
- respiratory tract