Literature DB >> 29130132

In vivo assessment of polydatin, a natural polyphenol compound, on arsenic-induced free radical overproduction, gene expression, and genotoxicity.

Damla Arslan-Acaroz1, Fahriye Zemheri2, Hasan Huseyin Demirel3, Ismail Kucukkurt1, Sinan Ince4, Abdullah Eryavuz5.   

Abstract

Arsenic (As) is a well-known contaminant of global groundwater. Its exposure causes several hazardous effects on animals and human via oxidative stress. The present study examined the effect of polydatin (PD) on free radical overproduction in rats exposed to As. Thirty-five male rats randomly allocated into five equal groups. To the control group, physiological saline was given orally and to the second group only 100 mg/L As was given by drinking water for 60 days. The other groups were treated with As (100 mg/L) and PD orally at 50, 100, and 200 mg/kg/day, respectively. Treatment with As enhanced malondialdehyde level but decreased glutathione level in blood, liver, kidney, brain, lung, and heart of rats. Also, As decreased superoxide dismutase and catalase activities of erythrocyte, liver, kidney, brain, lung, and heart in rats. Furthermore, As treatment gave rise to increased DNA damage and gene expressions of interleukin 1 beta (IL-1β), nuclear factor kappa beta (NFκB), p53, and tumor necrosis factor-α (TNF-α) in the lung, brain, kidney, and liver. However, treatment of PD ameliorated As-exposed lipid peroxidation, antioxidant enzymes activities, DNA damage, gene expressions, and histopathological changes in tissues. In conclusion, PD has a dose-dependent protective effect on lipid peroxidation and antioxidant defense mechanism in rats against As exposure.

Entities:  

Keywords:  Arsenic; DNA damage; Gene expression; Oxidative stress; Polydatin; Rat

Mesh:

Substances:

Year:  2017        PMID: 29130132     DOI: 10.1007/s11356-017-0391-6

Source DB:  PubMed          Journal:  Environ Sci Pollut Res Int        ISSN: 0944-1344            Impact factor:   4.223


  33 in total

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4.  Low-level arsenite induced gene expression in HEK293 cells.

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Journal:  Toxicology       Date:  2003-05-01       Impact factor: 4.221

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6.  A simple method for clinical assay of superoxide dismutase.

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Journal:  Clin Chem       Date:  1988-03       Impact factor: 8.327

7.  Dithiothreitol enhances arsenic trioxide-induced apoptosis in NB4 cells.

Authors:  J R Gurr; D T Bau; F Liu; S Lynn; K Y Jan
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8.  Low levels of arsenic trioxide stimulate proliferative signals in primary vascular cells without activating stress effector pathways.

Authors:  A Barchowsky; R R Roussel; L R Klei; P E James; N Ganju; K R Smith; E J Dudek
Journal:  Toxicol Appl Pharmacol       Date:  1999-08-15       Impact factor: 4.219

9.  Subchronic exposure to arsenic through drinking water alters expression of cancer-related genes in rat liver.

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  5 in total

1.  The subchronic exposure to malathion, an organophosphate pesticide, causes lipid peroxidation, oxidative stress, and tissue damage in rats: the protective role of resveratrol.

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2.  Update on Toxic Neuropathies.

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4.  Anxiolytic and anti-inflammatory role of thymoquinone in arsenic-induced hippocampal toxicity in Wistar rats.

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Review 5.  Polydatin: A Critical Promising Natural Agent for Liver Protection via Antioxidative Stress.

Authors:  Dandan Tang; Qing Zhang; Huxinyue Duan; Xun Ye; Jia Liu; Wei Peng; Chunjie Wu
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  5 in total

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