Copyright
©2014 Baishideng Publishing Group Inc.
World J Cardiol. Jun 26, 2014; 6(6): 367-375
Published online Jun 26, 2014. doi: 10.4330/wjc.v6.i6.367
Published online Jun 26, 2014. doi: 10.4330/wjc.v6.i6.367
Effect | Species | Drug |
Relaxation | Porcine | G-1[36,46] |
ICI182,780[35,36] | ||
Raloxifene[37] | ||
Tamoxifen[73] | ||
Rabbit | Raloxifene[54] | |
Tamoxifen[74] | ||
Endothelial NO production | Porcine | G-1[36] |
Raloxifene[54] | ||
Tamoxifen[74] | ||
CASMC BKCa channel opening | Porcine | G-1[46] |
Raloxifene[37] | ||
Tamoxifen[10] | ||
Human | G-1[46] | |
Inhibition of CASMC proliferation | Porcine | G-1[47] |
Human | G-1[47] | |
Inhibition of CASMC migration | Porcine | G-1[47] |
- Citation: Han G, White RE. G-protein-coupled estrogen receptor as a new therapeutic target for treating coronary artery disease. World J Cardiol 2014; 6(6): 367-375
- URL: https://www.wjgnet.com/1949-8462/full/v6/i6/367.htm
- DOI: https://dx.doi.org/10.4330/wjc.v6.i6.367