11-9-2001
Contact:
Karen N. Peart
karen.peart@yale.edu
203-432-1326
Yale University
Yale
researchers have shown for the first time that a component of the medicinal herb
feverfew targets a protein called IkappaB Kinase and halts that protein’s role
in the inflammation process.
"The
results pave the way for the development of novel anti-inflammatory drugs for a
variety of illnesses and symptoms, such as headache, swelling, redness and
inflammation," said Craig Crews, associate professor of molecular, cell and
developmental biology, chemistry and pharmacology at Yale.
Feverfew,
which is commonly used as an alternative medicine for migraine headaches, and
some other anti-inflammatory medicinal herbs, are rich in a group of compounds
thought to mediate the anti-inflammatory nature of these plants. The
anti-inflammatory component in feverfew is called parthenolide.
Led
by Crews, the research team set out to identify the molecular basis of
parthenolide’s anti-inflammatory activity. Through a combination of chemical
and biochemical approaches, the team made a derivative of parthenolide, which
they used to look for proteins that bind to parthenolide. They found that
IkappaB Kinase was one such binding protein, which is responsible for
inflammation.
"We
showed that the binding disrupted the protein’s ability to function, and we
also were able to identify the part of the protein to which the compound
binds," said Crews, whose study results are published in the August issue
of Chemistry and Biology. "Now that we have identified one inhibitor of
this protein, that information can be used to develop additional inhibitors.
This is important because a single inhibitor may not always make a successful
drug due to side effects, so it’s always useful to have a series of
inhibitors."