Many patients with hypertension are treated with ACE inhibitors. These
drugs block the angiotensin converting enzyme (ACE) that regulates the
salt and water balance of the body and raises blood pressure. Recent
studies by a research team led by Professor Ken Bernstein (Cedars-Sinai
Medical Center, Los Angeles, California, USA) have, however,
significantly broadened the enzyme's known task spectrum: The enzyme
also plays a key role in blood formation, renal development and male
fertility. In addition, the researchers showed that ACE has a hitherto
unexpected influence on the immune response.
At the 1st ECRC "Franz-Volhard" Symposium on Sept. 7, 2012 at the Max
Delbrück Center for Molecular Medicine (MDC) in Berlin-Buch, Professor
Ken Bernstein reported that in mice an excess of ACE led to a much
stronger immune response than usual. In animal experiments, not only
could bacterial infections be combated more effectively, but also the
growth of aggressive skin cancer (melanoma) in mice could be contained
by a stronger response of the immune system. In contrast, if the mice
lacked ACE, the immune cells worked less effectively.
In addition, ACE apparently has an influence on blood formation. It
has been known for many years that, in humans, ACE inhibitors induce a
small reduction of red blood cell levels. To elucidate the exact roles
of ACE, the Bernstein's research team deactivated the genes in mice that
normally provide the blueprint for the enzyme. As a consequence, these
so-called "knock out" mice could no longer produce the enzyme. The
examination of these mice revealed that they in fact had significantly
fewer red blood cells. Also, the white blood cells in these animals were
less functional. According to the researchers' studies, ACE evidently
plays a role in the development of the different blood cells.
Bernstein's team also showed that ACE apparently plays an important
role in the development of the kidneys. In mice that could not produce
the enzyme, the small arteries and the tissue of the kidneys revealed
pathological changes, and the urine flow was impaired.
According to these findings, male fertility is also associated with
ACE. Male mice lacking ACE continued to produce sperm, but they were no
longer able to reproduce. However, if in the mice not the enzyme itself,
but rather a product of ACE -- namely the hormone angiotensin II -- was
suppressed, they could continue to reproduce. Until now it was thought
that ACE mainly exerts its effect through the production of angiotensin
II. These results show, however, that ACE is enzymatically active and
produces other active products apart from angiotensin II, for example in
the testes.
Story Source:
The above story is reprinted from materials provided by Max Delbrück Center for Molecular Medicine.
Courtesy: ScienceDaily
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