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Vol. 60, Issue 2, 267-273, August 2001
Department of Pharmacology, Institute of Pharmaceutical Sciences,
University of Tübingen, Tübingen, Germany
Commercially available extracts from Boswellia
serrata resin used as anti-inflammatory drugs or
phytonutrients show paradoxical concentration-dependent potentiating
and inhibitory actions on 5-lipoxygenase (5-LO) product synthesis in
stimulated PMNs. In our attempt to characterize the stimulating
constituents, we identified the tetracyclic triterpene 3-oxo-tirucallic
acid (3-oxo-TA), which, in the range from 2.5 to 15 µM, enhanced 5-LO
product formation in ionophore-challenged polymorphonuclear cells
(PMNs) (e.g., from 1981 ± 177 to 3042 ± 208 pmol at 10 µM
3-oxo-TA), and initiated Ca2+ mobilization, MEK-1/2
phosphorylation, 5-LO translocation, and 5-LO product formation in
resting cells (534 ± 394 pmol/5 × 106 PMNs). In
cell-free 5-LO assays, 3-oxo-TA acted only inhibitory (IC50
value of about 3 µM), demonstrating the pivotal role of intact cell
structure for its activating property. In 3-oxo-TA-challenged PMNs, the
mitogen-activated protein kinase kinase (MEK)-1/2 inhibitor PD098059
abolished 5-LO product formation, along with inhibition of MEK-1/2
phosphorylation and 5-LO translocation. The 3-acetoxy derivative of
3-oxo-TA acted like 3-oxo-TA in intact PMNs, whereas 3-hydroxy-TA
barely stimulated MEK phosphorylation in resting cells and showed only
inhibition on ionophore-induced 5-LO product synthesis. Steroid-type
tetracycles neither induced 5-LO activation nor had enhancing or
inhibitory effects. In summary, defined natural tetracyclic
triterpenes, which act as inhibitors of the 5-LO in the cell-free
assay, initiate 5-LO activation by a MEK-inhibitor sensitive mechanism
and potentiate stimulated product synthesis in intact cells. Because
TAs contribute significantly to the overall biological effects of
B. serrata resin extracts, special precaution for
standardization is recommended when using B. serrata
preparations as drugs or dietary supplements.