Tanshinone IIA Attenuates H2O2-Induced Injury in Human Umbilical Vein Endothelial Cells

Author:

Chan Paul12,Chen Yen-Cheng32,Lin Li-Jen4,Cheng Tzu-Hurng5,Anzai Kazunori6,Chen Yin-Han7,Liu Zhong-Min8,Lin Jaung-Geng4,Hong Hong-Jye4

Affiliation:

1. Division of Cardiovascular Medicine, Department of Internal Medicine, Taipei Medical University, Taipei, Taiwan, R.O.C.

2. Department of Cardiology, St. Mary's Hospital, Lotung, Yi-Lan County, Taiwan, R.O.C.

3. Division of Nephrology, Wan Fang Hospital, Taipei Medical University, Taipei, Taiwan, R.O.C.

4. School of Chinese Medicine, College of Chinese Medicine, China Medical University, Taichung, Taiwan, R.O.C.

5. Department of Biological Science and Technology, College of Life Sciences, China Medical University, Taichung, Taiwan, R.O.C.

6. Faculty of Pharmaceutical Sciences, Nihon Pharmaceutical University, Saitama, Japan

7. Department of Cardiology, Tongji University, Shanghai, China

8. Department of Cardiac Surgery, Shanghai East Hospital, Tongji University, Shanghai, China

Abstract

The injury of endothelial cell is the critical event of vascular disease. In endothelial cell, oxidative stress is regarded as critical to pathogenic factors in endothelial cell injury and apoptosis. Tanshinone IIA is the main effective component of Salvia miltiorrhiza known as "Danshen" in traditional Chinese medicine for treating cardiovascular disorders, but the mechanism by which it exerts the protective effect is not well established. The present study was designed to test the hypothesis that tanshinone IIA can inhibit hydrogen peroxide ( H2O2 )-induced injury and unravel its intracellular mechanism in human umbilical vein endothelial cells (HUVECs). In this study, HUVECs were treated with tanshinone IIA in the presence/absence of H2O2 . The protective effects of tanshinone IIA against H2O2 were evaluated. Our results show that HUVECs incubated with 200 μM H2O2 had significantly decreased the viability of endothelial cells, which was accompanied with apparent cell apoptosis, the activation of caspase-3 and the upregulation of p53 expression, which was known to play a key role in H2O2 -induced cell apoptosis. However, pretreatment with tanshinone IIA (3–10 μM) resulted in a significant resistance to H2O2 -induced apoptosis. In addition, pretreatment with tanshinone IIA decreased the activity of caspase-3 and p53 expression. Tanshinone IIA also induced activating transcription factor (ATF) 3 expression; while knockdown of ATF-3 with ATF-3 siRNAsignificantly reduced tanshinone IIA's protective effect. In conclusion, the present study shows that tanshinone IIA can protect endothelial cells against oxidative injury induced by H2O2 , suggesting that this compound may constitute a promising intervention against cardiovascular disorders and ATF-3 may play an important role in this process.

Publisher

World Scientific Pub Co Pte Lt

Subject

Complementary and alternative medicine,General Medicine

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