Abstract
The biosynthesis of leukotrienes (LTs) is initiated by the transformation of free
arachidonic acid to LTA4 by 5-lipoxygenase (5-LO). Subsequent enzymatic conversion of LTA4 yields LTB4 and the cysteinyl-LTs C4, D4 and E4. LTs have prominent functions in pathophysiology and are connected to numerous disorders
including bronchial asthma, allergic rhinitis, inflammatory bowel and skin diseases,
rheumatoid arthritis, cancer, osteoporosis and cardiovascular diseases. Pharmacological
and genetic interruption of the 5-LO pathway or blockade of LT receptors, serving
as means for intervention with LTs, may be of therapeutic value for certain related
disorders. Natural or plant-derived substances were among the first 5-LO inhibitors
identified in the early 1980 s. To date, a huge number of diverse plant-derived compounds
have been reported to interfere with 5-LO product synthesis. However, many investigations
have addressed the efficacy of a given compound solely in cellular test systems and
analysis of direct interference with 5-LO has been neglected. In the first part of
this review, the biology and molecular pharmacology of the 5-LO pathway is summarized
in order to understand its overall regulation and complexity as well as to comprehend
the possible points of attack of compounds that eventually lead to inhibition of 5-LO
product formation in intact cells. In the second part, natural compounds that interfere
with 5-LO product formation are compiled and grouped into structural classes, and
the underlying molecular mechanisms and structure-activity relationships are discussed.
Abbreviations
AA:arachidonic acid
CLP:coactosine-like potein
COX:cyclooxygenase
GPCR:G protein-coupled receptor
GPX:glutathione peroxidase
GSH:glutathione
FLAP:5-lipoxygenase-activating protein
H(P)ETE:hydro(pero)xyeicosatetraenoic acid
iNOS:inducible nitric oxide synthase
LO:lipoxygenase
LOOH:lipid hydroperoxide
LT:leukotriene
MAPEG:membrane-associated proteins in eicosanoid and
glutathione metabolism
MAPK:mitogen-activated protein kinase
NDGA:nordihydroguaiaretic acid
NFκB:nuclear factor κB
PAF:platelet-activating factor
fMLP:N-formyl-methionyl-leucyl-phenylalanine
PC:phosphatidylcholine
PL:phospholipase
PK:protein kinase
PMNL:polymorphonuclear leukocytes
PT:pentacylic triterpene
SAR:structure-activity relationships
Key words
5-Lipoxygenase - arachidonic acid - leukotrienes - leukocytes - inflammation - plants
- natural compounds - inhibitors
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Prof. Dr. Oliver Werz
Department of Pharmaceutical Analytics
Pharmaceutical Institute
Eberhard-Karls-University Tuebingen
Auf der Morgenstelle 8
72076 Tuebingen
Germany
Phone: +49-7071-297-8793
Fax: +49-7071-294-565
Email: oliver.werz@uni-tuebingen.de