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Aim:
To investigate the effects of salvianolate, a water-soluble active compound from
Salvia miltiorrhiza
Bunge, on reactive oxygen species (ROS) production in mouse cardiomyocytes
in vitro
.
Methods:
Primary ventricular cardiomyocytes were prepared from neonatal mouse. The cell viability was determined using MTT assay. Culture medium for each treatment was collected for measuring the levels of NO, iNOS, total antioxidant capacity (TAOC) and transforming growth factor β1 (TGFβ1). TGFβ1 and Smad2/3 expression in the cells was detected with Western blotting.
Results:
H
2
O
2
(1.25 mmol/L) did not significantly affect the cell viability, whereas the high concentration of salvianolate (5 g/L) alone dramatically suppressed the cell viability. Treatment of the cells with H
2
O
2
(1.25 mmol/L) markedly increased ROS and iNOS production, and decreased the levels of NO, TAOC and TGFβ1 in the culture medium. Furthermore, the H
2
O
2
treatment significantly increased TGFβ1 and Smad2/3 expression in the cells. Addition of salvianolate (0.05, 0.1, and 0.5 g/L) concentration-dependently reversed the H
2
O
2
-induced alterations in the culture medium; addition of salvianolate (0.05 g/L) reversed the H
2
O
2
-induced increases of TGFβ1 and Smad2/3 expression in the cells. Blockage of TGFβ1 with its antibody (1 mg/L) abolished the above mentioned effects of salvianolate.
Conclusion:
Salvianolate inhibits ROS and iNOS production and increases TAOC and NO levels in H
2
O
2
-treated cardiomyocytes
in vitro
via downregulation of Smad2/3 and TGFβ1 expression. High concentration of salvianolate causes cytotoxicity in mouse cardiomyocytes.