Iizuka Toru, Nagai Masahiro
The Faculty of Pharmaceutical Sciences, Hoshi University, Tokyo 142-8501, Japan.
Yakugaku Zasshi. 2005 Feb;125(2):219-24. doi: 10.1248/yakushi.125.219.
The vasorelaxant effects of forsythiaside (compound 1) from the fruits of Forsythia suspensa on isolated rat aortic rings were studied. Compound 1 showed a slow relaxation activity against norepinephrine (NE)-induced contractions of rat aorta with/without endothelium. This compound did not affect contractions induced by a high concentration of potassium (K(+) 60 mM), while it inhibited NE-induced vasocontraction in the presence of nicardipine. These results show that the inhibition by compound 1 of NE-induced vasocontraction is due to a decrease in calcium influx from the extracellular space caused by NE.