Abstract

The beneficial effects of green tea polyphenols (GTPs) on D-galactose (D-Gal)-induced liver aging in male Kunming mice were investigated. For this purpose, 40 adult male Kunming mice were divided into four groups. All animals, except for the normal control and GTPs control, were intraperitoneally injected with D-galactose (D-Gal; 300 mg/kg/day for 5 days a week) for 12 consecutive weeks, and the D-Gal-treated mice were allowed free access to 0.05% GTPs (w/w) diet or normal diet for 12 consecutive weeks. Results showed that GTP administration improved the liver index and decreased transaminases and total bilirubin levels. Furthermore, GTPs significantly increased hepatic glutathione and total antioxidant levels, and the activities of superoxide dismutase, catalase, and glutathione S-transferase (GST). Furthermore, GTPs downregulated 8-hydroxy-2-deoxyguanosine, advanced glycation end products, and hepatic oxidative stress markers, such as malondialdehyde and nitric oxide. Additionally, GTPs abrogated dysregulation in hepatic Kelch-like ECH-associated protein 1 and nuclear factor erythroid 2-related factor 2 (Nrf2) and its downstream target gene expression [heme oxygenase 1, NAD(P)H:quinone oxidoreductase 1, and GST] and inhibited tumor necrosis factor-α, transforming growth factor-β, and interleukin (IL)-1β and IL-6 in the liver of treated mice. Finally, GTPs effectively attenuated D-Gal-induced edema, vacuole formation, and inflammatory cell infiltration. In conclusion, GTPs showed antioxidant and anti-inflammatory properties in D-Gal-induced aging mice, and may be considered a natural alternative to the effects of hepatic aging.

Highlights

  • Aging is one kind of irreversible and perennial natural biological process that accounts for genetic, internal, and external environmental factors

  • High doses of D-Gal can induce the formation of hydrogen peroxide, which is invariably linked to reactive oxygen species (ROS), leading to hepatic metabolic disorders and, liver aging [23, 24]

  • The hepatic antioxidant system plays an important role in maintaining the normal liver function, and changes in antioxidants in this system impact the endogenous antioxidant capacity [24]

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Summary

Introduction

Aging is one kind of irreversible and perennial natural biological process that accounts for genetic, internal, and external environmental factors. This process is characterized by a progressive loss of physiological integrity, which invariably leads to impairments in the organizational structure and function of organs [1]. Aging-related liver diseases mainly include alterations of hepatic structure and function, where the increase of liver volume and decrease of hepatic blood flow and perfusion occur. These changes increase the liver fibrosis, hepatocarcinoma, and mortality rate of susceptible elderly people and can be considered adverse prognostic factors [3– 5]. Strategies to counteract/alleviate the harmful effects of aging on liver function are desired from the public health perspective

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