Effects of caffeic acid phenethyl ester (CAPE) on membrane potential and intracellular calcium in human endothelial cells
dc.authorwosid | Aydogdu, Nurettin/ABH-9224-2020 | |
dc.contributor.author | Burgazli, M. Kamil | |
dc.contributor.author | Aydogdu, N. | |
dc.contributor.author | Rafiq, A. | |
dc.contributor.author | Mericliler, M. | |
dc.contributor.author | Chasan, R. | |
dc.contributor.author | Erdogan, A. | |
dc.date.accessioned | 2024-06-12T10:55:28Z | |
dc.date.available | 2024-06-12T10:55:28Z | |
dc.date.issued | 2013 | |
dc.department | Trakya Üniversitesi | en_US |
dc.description.abstract | BACKGROUNG AND OBJECTIVES: Caffeic acid phenethyl ester (CAPE) is an active component of the resin propolis obtained from beehives. Propolis has a long history of medicinal use and a number of studies have already reported on some of its pharmaceutical properties. This study aimed to explore the effects of CAPE on the cytosolic Ca2+ concentration, cell proliferation, membrane potential and NO levels in human endothelial cells. MATERIALS AND METHODS: Isolated human umbilical vein endothelial cells (HUVEC) were incubated with CAPE (1-100 mu M) at 37 degrees C for 48 hours. Cell proliferation was estimated by counting cell numbers with use of a Neubauer chamber. The effect of CAPE (1-100 mu M) on the membrane potential was measured with the fluorescence dye DIBAC4(3) whereas its effect on the cytosolic Ca2+ concentration was measured by use of the fluorescence probe Fluo-3 AM (Invitrogen, Leiden, Netherlands). NO production was assayed using the flourophore DAF similar to AM (Invitrogen, Leiden, Netherlands). Changes in fluorescence intensity was determined with the GENios plate reader (Genios, Tecan, Austria). RESULTS: A Dose-dependent hyperpolarization of the endothelial cell membrane was observed with CAPE stimulation. The initial increase in the intracellular Ca2+ concentration showed a subsequent decrease over time. CAPE stimulation also resulted in an increase in NO production; however, at higher doses a decrease in NO levels was observed. HUVEC proliferation was inhibited by CAPE. CONCLUSIONS: Here we report on the effect of CAPE stimulation on the cytosolic Ca2+ concentration, cell proliferation, membrane potential and NO production in HUVEC in a dose-dependent manner. These findings provide important insights into some potential key roles that both calcium and the membrane potential play in the CAPE activation of endothelial cells in a concentration-dependent manner. | en_US |
dc.identifier.endpage | 728 | en_US |
dc.identifier.issn | 1128-3602 | |
dc.identifier.issue | 6 | en_US |
dc.identifier.pmid | 23609354 | en_US |
dc.identifier.scopus | 2-s2.0-84878585529 | en_US |
dc.identifier.scopusquality | Q2 | en_US |
dc.identifier.startpage | 720 | en_US |
dc.identifier.uri | https://hdl.handle.net/20.500.14551/19439 | |
dc.identifier.volume | 17 | en_US |
dc.identifier.wos | WOS:000325207900002 | en_US |
dc.identifier.wosquality | Q4 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.publisher | Verduci Publisher | en_US |
dc.relation.ispartof | European Review For Medical And Pharmacological Sciences | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Caffeic Acid Phenthyl Ester | en_US |
dc.subject | Endothelial Cells | en_US |
dc.subject | Calcium | en_US |
dc.subject | Mebrane Potential | en_US |
dc.subject | Nitric-Oxide Production | en_US |
dc.subject | Heme Oxygenase-1 | en_US |
dc.subject | Apoptosis | en_US |
dc.subject | Proliferation | en_US |
dc.subject | Angiogenesis | en_US |
dc.subject | Conductance | en_US |
dc.subject | Suppression | en_US |
dc.subject | Induction | en_US |
dc.subject | Propolis | en_US |
dc.subject | Channels | en_US |
dc.title | Effects of caffeic acid phenethyl ester (CAPE) on membrane potential and intracellular calcium in human endothelial cells | en_US |
dc.type | Article | en_US |