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. 2017 Jun 30;50(6):323–328. doi: 10.5483/BMBRep.2017.50.6.182

Fig. 2.

Fig. 2

Effects of lysophosphatidylcholine (LPC) on intracellular calcium concentration ([Ca2+]i) in human umbilical vein endothelial cells (HUVECs). (A) LPC increased [Ca2+]i dose-dependently in a 1.8 mmol/L Ca2+ bathed-external solution. (B) The effects of LPC on [Ca2+]i depend on the external Ca2+ in HUVECs. LPC induced only an initial transient peak of [Ca2+]i in the absence of external Ca2+ and did not elicit the increase of [Ca2+]i under treatment with endoplasmic reticulum blockers: 50 μmol/L dantrolene and 10 μmol/L U73122. The sustained [Ca2+]i increase represents Ca2+ influx from the extracellular solution. (C) Effects of chlorogenic acid (CGA) on LPC-induced [Ca2+]i in HUVECs. The CGA blocked the LPC-induced sustained [Ca2+]i increase. (D) No effect of CGA without LPC in HUVECs. CGA (300 μmol/L and 1,000 μmol/L) was treated without Ca2+ and with 1.8 mM Ca2+ in HUVECs. Data are the mean values of three independent experiments.