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Inhibitory effect of acteoside on melittin-induced catecholamine exocytosis through inhibition of Ca2+-dependent phospholipase A(2) and extracellular Ca2+ influx in PC12 cells

Authors
Song, Ho SunKo, Myung SooJo, Young SooWhang, Wan KyunnSim, Sang Soo
Issue Date
Oct-2015
Publisher
PHARMACEUTICAL SOC KOREA
Keywords
Acteoside; Arachidonic acid; Catecholamine; Ca2+ mobilization; Chromogranin A; Phospholipase A(2)
Citation
ARCHIVES OF PHARMACAL RESEARCH, v.38, no.10, pp 1913 - 1920
Pages
8
Journal Title
ARCHIVES OF PHARMACAL RESEARCH
Volume
38
Number
10
Start Page
1913
End Page
1920
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/9048
DOI
10.1007/s12272-015-0601-z
ISSN
0253-6269
1976-3786
Abstract
To investigate the inhibitory effect of acteoside on the process of exocytosis induced by melittin, we measured Ca2+ mobilization, arachidonic acid (AA) release and catecholamine exocytosis in PC12 chromaffin cells. Melittin significantly increased the intracellular Ca2+ mobilization via receptor-operated calcium channel but not the intracellular Ca2+ release. It caused AA release via activation of Ca2+-dependent phospholipase A(2) (PLA(2)) and catecholamine secretion in a dose-dependent manner. Acteoside dose-dependently inhibited the release of AA and intracellular Ca2+ mobilization induced by melittin. Acteoside reduced the catecholamine release and raised the amount of intracellular chromogranin A which is co-released with catecholamine from melittin-stimulated PC12 cells. Taken together, our results suggest that acteoside could suppress the exocytosis via inhibition of Ca2+-dependent PLA(2) and extracellular Ca2+ influx in PC12 cells stimulated by melittin.
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