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Ginsenoside Rg1 reduces toxicity of fine particulate matter on human alveolar epithelial cells: A preliminary observation.

Authors :
ZHI-GUO ZHANG
XU-YAN NIU
XIAO-JUAN HE
JUN SHU
Source :
Molecular Medicine Reports; 2014, Vol. 9 Issue 3, p989-992, 4p
Publication Year :
2014

Abstract

Fine particulate matter (PM<subscript>2.5</subscript>) is a significant environmental pollutant responsible for a number of human diseases. Ginsenoside Rg1 (Rg1) is likely to have the potential to relieve PM<subscript>2.5</subscript>-induced cell injury. The present study is designed to preliminarily observe the harmful effect of PM<subscript>2.5</subscript> and the protective effect of Rg1 against PM<subscript>2.5</subscript> on human A549 lung epithelial cells in vitro. The cytotoxic effects of the PM<subscript>2.5</subscript> or Rg1 on A549 cells were measured by means of cell viability, and then exposure concentration of PM<subscript>2.5</subscript> and pretreatment concentration of Rg1 used in the following assays were established. The A549 cells were pretreated with Rg1 for 1 h and then exposed to PM<subscript>2.5</subscript> for 24 h. The levels of lactate dehydrogenase (LDH) in the cell culture supernatant and malondialdehyde (MDA) within the cells were assayed. The present results revealed that 200-1,200 μg/ml of PM<subscript>2.5</subscript> decreased the viability of A549 cells significantly in a concentration-dependent manner; however, 50-400 μg/ml of Rg1 had no significant effect. Pretreatment with 100, 200 or 400 μg/ml Rg1 significantly diminished the 200 μg/ml PM<subscript>2.5</subscript>-induced A549 cell viability and decreased LDH leakage and MDA generation in a concentration-dependent manner. These results indicated that PM<subscript>2.5</subscript> induced cell injury and Rg1, antagonized PM<subscript>2.5</subscript>-induced cell injury to a certain extent. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17912997
Volume :
9
Issue :
3
Database :
Complementary Index
Journal :
Molecular Medicine Reports
Publication Type :
Academic Journal
Accession number :
95982326
Full Text :
https://doi.org/10.3892/mmr.2013.1870