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Jerusalem Post (Israel), 2006-06-14 (Wed) Israeli Researcher Lowers Blood Pressure with Cannabis Component by Judy Siegel
A new method for lowering blood pressure with a compound that
synthesizes a cannabis (hashish or marijuana) plant component has
been developed by a Hebrew University doctoral student in pharmacology.
For his work on the cardiovascular activity of cannabinoids
(chemical compounds derived from cannabis), Yehoshua Maor has been
named one of the winners of this year's Kaye Innovation Awards, to
be presented on Tuesday during the university's 69th annual board of
governors meetings.
The Kaye Innovation Awards, established by British pharmaceutical
industrialist Isaac Kaye, have been given annually since 1994 to
encourage HU faculty, staff and students to develop innovative
methods and inventions with good commercial potential to benefit the
university and society.
Not all patients respond well to conventional hypertension drugs.
But the cannabis plant, through its chemical compounds, has been
shown to have a beneficial, hypotensive effect.
But a drawback in the therapeutic use of cannabinoids has been the
undesirable psychotropic properties such as hallucinatory effects.
Attempts to separate the hypotensive action from their psychotropic
properties have been only partially successful until now.
Working under the supervision of Prof. Raphael Mechoulam at the HU
School of Pharmacy, Maor - a native of Brazil who immigrated to
Israel in 1998 - has created a synthetic version of a minor cannabis
constituent named cannabigerol, which is devoid of psychotropic
activity. In laboratory experiments with rats, in collaboration with
Prof. Michal Horowitz, it was found that this novel compound reduced
blood pressure when administered in relatively low doses.
Additional testing also showed that the compound also brought about
another beneficial effect - relaxation of the blood vessels.
A further beneficial property observed in work carried out with
Prof. Ruth Gallily was that the compounds produced an
anti-inflammatory response.
Maor says these qualities could be combined to create a valuable new
clinical drug with major market potential, especially for diabetic
patients suffering from hypertension, since reductions in blood
pressure can decrease the risk of diabetes complications and in
others with metabolic irregularities.
Meanwhile, former Russian immigrant Elena Khazanov, 34, will also
receive a Kaye Prize for developing a novel method for combining two
anti-cancer drugs into a single delivery system, thereby
dramatically improving treatment efficacy.
Khazanov, who arrived here 12 years ago, developed her drug delivery
system as a PhD student under the tutelage of Prof. Yechezkel
Barenholz of the Hebrew University-Hadassah Medical School's
biochemistry department.
Khazanov used an approach called combination therapy, in which two
or more agents are introduced within a single delivery unit, with
the result that the combination has a better beneficial
chemotherapeutic effect than otherwise would be possible.
Her work was based on the previous success of HU scientists with the
delivery system for an anti-cancer drug, doxorubicin (DXR), which
resulted in development of DXR delivery through sterically
stabilized liposomes (SSL), which are ball-like fatty molecules.
A highly successful medication based on that research has been
manufactured by SEQUUS Pharmaceuticals and is marketed as Doxil.
Khazanov aimed to combine DXR with ceramides, a family of fatty
molecules found in high concentrations within cell membranes.
These act as signaling molecules, triggering programmed cell death
in many types of cancer cells.
However, the physical and chemical properties of ceramides make them
unusable by themselves for therapeutic application in vivo. Her
efforts ultimately proved successful in formulating a novel drug
delivery system consisting of SSL that contained both DXR and ceramides.
In laboratory tests on mice, the synergism between the two drugs
resulted in an improved therapeutic benefit over Doxil alone.
The fact that both were delivered by one tiny SSL liposome enables
long plasma circulation time and liposome-selective delivery to the
tumor site by their introduction into the tumor through pores
present in the tumor blood vessels.
Additional trials, including therapeutic efficacy studies in mice
bearing different tumors, plus toxicology studies of this new
liposome formulation, are continuing to ultimately enable human
clinical trials. Patents have been secured through Yissum, HU's
technology transfer company, to enable further development of the
delivery system. New, non-invasive therapies for treating diseases
such as basal cell carcinoma, viral and microbial deep skin
infections and erectile dysfunction are being developed by Prof.
Elka Touitou, another Kaye Prize recipient from the pharmacy school.
The new approach uses a specially designed, patented topical
delivery system known as Ethosome for targeting drugs directly to
the disease site. Touitou invented the system with a group of her
students and postdoctoral fellows.
Ethosome provides a dermal delivery system that overcomes the
natural skin barrier that has prevented anti-cancer drugs applied on
the skin from reaching their targets.
Drugs encased in Ethosome are able to penetrate even into the deep
skin layers where basal carcinoma cells occur, thereby providing a
non-invasive alternative to surgical intervention. A number of
clinical studies, including a recent one on the use of
Ethosomalprostaglandin for treatment of impotence, have shown their
efficiency, and the delivery system can be used in cosmetic compounds.
v
New and safer compounds for treatment of epilepsy patients and those
suffering from other neural disorders have been developed by Prof.
Meir Bialer and Prof. Boris Yagen. Their work at the pharmaceutics,
medicinal chemistry and natural products department at the pharmacy
school is also being recognized by a Kaye Prize they will share.
They developed a potential alternative for valproic acid (VPA), one
of the leading anti-epileptic drugs, which has been used as a
central nervous system treatment since 1967, but which also has
serious safety drawbacks. Its side effects can cause damage
especially to children or women of child-bearing age. Patents have
been obtained by Yissum.
The Barenholz Prize for Creativity and Originality in Applied
Research will be presented to a 29-year-old HU doctoral student at
the pharmacy school, for her work in discovering a way to prevent
restenosis - recurrent blocking of coronary arteries after
angioplasty (balloon therapy).
The award, named for its donor, cancer researcher Prof. Yehezkel
Barenholz, will be presented during the board meetings to Hila
Epstein-Barash. In her research, she and her colleagues hypothesized
that if the macrophages that accumulate in the area of the
angioplastic treatment could be inactivated, the problem could be solved.
The problem was how to deliver a cell-specific drug that could
achieve this. In their research they found that this could be
accomplished through the use of bisphosphonates - bone-seeking
agents used clinically to treat osteoporosis - which have high
affinity to calcium and are assimilated into bone tissue by
osteoclasts - which are closely related to macrophages. The problem
before them was how to reach the targeted area of macrophages in the
blood vessels, since the drug alone, due to its chemical makeup, is
not able to cross cell membranes.
The researchers subsequently found that by encapsulating the
bisphosphonates in liposomes, the drug could be delivered to the
macrophages in the blood vessels that had been opened by
angioplasty. The scientists found that a single injection of
liposomes containing bisphosphonates, soon after angioplasty,
significantly prevented restenosis in rat and rabbit models,
markedly reducing the thickness of the inner wall of the affected
arteries and leaving enough room for the blood to circulate.
Pre-clinical trials are now proceeding in Australia, using this
procedure which is non-toxic and presents no side effects.
Pubdate: Wed., June 14, 2006 © 2006 Jerusalem Post |
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