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Inhibitory mechanism of Aloe single component(Alprogen) on the mediator release in the guinea pig lung mast cell activated with specific antigen-antibody reactions.

Authors
 Jai Youl Ro  ;  Byung Chul Lee  ;  Ji Young Kim  ;  Yean Jun Chung  ;  Myung Hee Chung  ;  Seung Kee Lee  ;  Tae Hyung Jo  ;  Kyung Hwan Kim  ;  Young In park 
Citation
 Journal of Pharmacology and Experimental Therapeutics, Vol.292(1) : 114-121, 2000 
Journal Title
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS
ISSN
 0022-3565 
Issue Date
2000
MeSH
Aloe/chemistry ; Animals ; Antigen-Antibody Reactions/physiology* ; Calcium/metabolism ; Cells, Cultured ; Cricetinae ; Diglycerides/metabolism ; Dose-Response Relationship, Drug ; Electrophoresis, Polyacrylamide Gel ; Female ; Fluorescence ; Histamine Release/drug effects ; Immunoglobulin G/pharmacology ; Inflammation Mediators/metabolism* ; Leukotrienes/secretion ; Lung/drug effects* ; Mast Cells/drug effects* ; Mast Cells/metabolism ; Microscopy, Confocal ; Ovalbumin/pharmacology ; Phospholipase D/metabolism ; Phospholipases A/metabolism ; Plant Extracts/isolation & purification ; Plant Extracts/pharmacology* ; Plants, Medicinal ; Protein Kinases/metabolism ; Radioimmunoassay ; Time Factors
Abstract
We previously reported that the glycoprotein extracted from aloe strongly inhibited the mediator releases caused by the activation of guinea pig lung mast cells. Therefore, this study aimed to purify a single component that has an antiallergic effect from crude aloe extract and then to assess the effects of aloe single component (alprogen) on the mechanism of mediator releases caused by the mast cell activation. We purified aloe extracts by using various columns. We also purified mast cells from guinea pig lung tissues by using enzyme digestion, rough and discontinuous density Percoll gradient. Mast cells were sensitized with IgG(1) (anti-ovalbumin) and challenged with ovalbumin. Histamine was assayed by using a fluorometric analyzer and leukotrienes by radioimmunoassay. [Ca(2+)](i) level was analyzed by using a confocal laser scanning microscope. Protein kinase activity was determined by the protein phosphorylated with [gamma-(32)P]ATP. The phospholipase D activity was assessed by the labeled phosphatidylalcohol. The amount of mass 1,2-diacylglycerol (DAG) was measured by the [(3)H]DAG produced when prelabeled with [(3)H]myristic acid. Phospholipase A(2) activity was determined by measuring the lyso-phosphatidylcholine released from the labeled phospholipids. Alprogen significantly decreased histamine and leukotriene releases and blocked completely Ca(2+) influx during mast cell activation. The protein kinase C and phospholipase D activities were decreased by alprogen in dose-dependent manner. Alprogen inhibited mass DAG formation and the phospholipase A(2) activity during mast cell activation. The data suggest that alprogen purified from aloe inhibits multiple signals as well as blocking Ca(2+) influx caused by mast cells activated with specific antigen-antibody reactions and that then the inhibition of histamine and leukotriene release follows.
Full Text
http://jpet.aspetjournals.org/content/292/1/114.long
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pharmacology (약리학교실) > 1. Journal Papers
Yonsei Authors
Kim, Kyung Hwan(김경환)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/171736
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