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자료유형
학술저널
저자정보
Lee, Jin-Hee (College of Pharmacy, Chung-Ang University) Lee, Ji-Yun (College of Pharmacy, Chung-Ang University) Kang, Hyo-Suk (College of Pharmacy, Chung-Ang University) Jeong, Chan-Hun (College of Pharmacy, Chung-Ang University) Moon, Hee (College of Pharmacy, Chung-Ang University) Whang, Wan-Kyunn (College of Pharmacy, Chung-Ang University) Kim, Chang-Jong (College of Pharmacy, Chung-Ang University) Sim, Sang-Soo (College of Pharmacy, Chung-Ang University)
저널정보
대한약학회 Archives of pharmacal research : a publication of the Pharmaceutical Society of Korea Archives of pharmacal research : a publication of the Pharmaceutical Society of Korea 제29권 제6호
발행연도
2006.1
수록면
508 - 513 (6page)

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The effect of acteoside, a phenylpropanoid glycoside isolated from Clerodendron trichotomum Thunberg, on histamine and arachidonic acid release was investigated in RBL 2H3 cells. Histamine was dose-dependently released from RBL 2H3 cells by melittin, arachidonic acid and thapsigargin. In extracellular $Ca^{2+}-free$ solution, basal secretion of histamins increased by two fold. The response of histamine release to melittin and thapsigargin in $Ca^{2+}-free$ solution was significantly decreased, whereas the response to arachidonic acid was significantly increased as compared with those in normal solution. Acteoside inhibited histamine release induced by melittin, arachidonic acid and thapsigargin in a dose-dependent manner in the presence or absence of extracellular $Ca^{2+}$. However, the inhibitory activity of acteoside was more potent in normal solution than that in $Ca^{2+}-free$ solution. These data suggest that inhibitory mechanism of acteoside on histamine release may be related to extracellular $Ca^{2+}$. On the other hand, acteoside significantly inhibited arachidonic acid release and prostaglandin $E_2$ production Induced by $0.5\;{\mu}M$ melittin. It is possible that acteoside may be developed as an anti-inflammatory agent.

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