Korean J Physiol Pharmacol.
1998 Apr;2(2):251-260.
Cromakalim blocks membrane phosphoinositide activated signals in the guinea pig lung mast cells stimulated with antigen-antibody reactions
- Affiliations
-
- 1Department of Pharmacology, Yonsei University College of Medicine, CPO Box 8044, Seoul 120-752, Korea.
Abstract
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Cromakalim (BRL 34915), known as an airway smooth muscle relaxant,
inhibited the releases of mediators in the antigen-induced mast cell
activation. It has been suggested that cromakalim, in part, inhibited
mediator releases by inhibiting the initial increase of
1,2-diacylglycerol (DAG) produced by the activation of the other
phospholipase system which is different from
phosphatidylcholine-phospholipase D pathway. The aim of this study is
to further examine the inhibitory mechanism of cromakalim on the
mediator release in the mast cell activation. Guinea pig lung mast
cells were purified by using enzyme digestion and percoll density
gradient. In purified mast cells prelabeled with (3H)PIP2,
phospholipase C (PLC) activity was assessed by the production of
(3H)insitol phosphates. Protein kinase C (PKC) activity was assessed by
measuring the protein phosphorylated from mast cells prelabeled with
(gamma-32P)ATP, and Phospholipase A2 (PLA2) activity by measuring the
lyso-phosphatidylcholine produced from mast cell prelabeled with
1-palmitoyl-2-arachidonyl phosphatidyl-(14C)choline. Histamine was
assayed by fluorometric analyzer, and leukotrienes by radioimmunoassay.
The PLC activity was increased by activation of the passively
sensitized mast cells. This increased PLC activity was decreased by
cromakalim pretreatment. The PKC activity increased by the activation
of the passively sensitized mast cells was decreased by calphostin C,
staurosporine and cromakalim, respectively. The PLA2 activity was
increased in the activated mast cells. The pretreatment of cromakalim
did not significantly decrease PLA2 activity. These data show that
cromakalim inhibits histamine release by continuously inhibiting signal
transduction processes which is mediated via PLC pathway during mast
cell activation, but that cromakalim does not affect PLA2 activity
related to leukotriene release.