ROTTEN EGG GAS HOLDS KEY TO HEALTH CARE THERAPIES
It may smell of flatulence and have a reputation for being highly toxic,
but when used in the right tiny dosage, hydrogen sulfide is now being being
found to offer potential health benefits in a range of issues, from diabetes to
stroke, heart attacks and dementia. A new compound (AP39), designed and made at
the University of Exeter, could hold the key to future therapies, by targeting
delivery of very small amounts of the substance to the right (or key) places
inside cells.
Scientists in Exeter
have already found that the compound protects mitochondria -- the
"powerhouse" of cells, which drive energy production in blood vessel
cells. Preventing or reversing mitochondrial damage is a key strategy for
treatments of a variety of conditions such as stroke, heart failure, diabetes
and arthritis, dementia and aging. Mitochondria determine whether cells live or
die and they regulate inflammation. In the clinic, dysfunctional mitochondria
are strongly linked to disease severity.
Professor Matt
Whiteman, of the University of Exeter Medical School, said: "When cells
become stressed by disease, they draw in enzymes to generate minute quantities
of hydrogen sulfide. This keeps the mitochondria ticking over and allows cells
to live. If this doesn't happen, the cells die and lose the ability to regulate
survival and control inflammation. We have exploited this natural process by
making a compound, called AP39, which slowly delivers very small amounts of
this gas specifically to the mitochondria. Our results indicate that if
stressed cells are treated with AP39, mitochondria are protected and cells stay
alive."
Dr. Mark Wood of
Biosciences, at the University of Exeter, added "Although hydrogen sulfide
is well known as a pungent, foul-smelling gas in rotten eggs and flatulence, it
is naturally produced in the body and could in fact be a healthcare hero with
have significant implications for future therapies for a variety of
diseases."
The research is
being conducted in several models of disease, and pre-clinical results are
promising. For example, in models of cardiovascular disease, research shows
that more than 80 per cent of the powerhouse mitochondria cells survive under
otherwise highly destructive conditions, if the AP39 is administered.
Professors Whiteman and Wood are now working towards advancing the research to
a stage where it can be tested in humans.
The study was
published in the journal Medicinal Chemistry Communications.
A follow-up study, published in The Nitric Oxide Journal with collaborators from the University
of Texas Medical Branch, also found that the compound selectively prevented
mitochondrial DNA in mitochondria. Once damaged, this DNA cannot be repaired,
leaving individuals more vulnerable to disease symptoms.
Early indications in
small-scale studies, presented at this year's 3rd International Conference on
Hydrogen Sulfide in Biology and Medicine in Kyoto, also show that in high blood
pressure, AP39 reversed blood vessel stiffening and lowered blood pressure. It
also dramatically improved chances of survival after a heart attack by slowing
the heartbeat, improving its efficiency.
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