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New Treatment Strategies to Combat Heart Failure
Sponsored by the APS Cardiovascular Section
Supported by the William Townsend Porter
Foundation
Tues. April 4 — 10:30 AM-12:30 PM
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| Chaired: |
David J. Lefer, LSU Hlth. Sci. Ctr.,
Shreveport
Rong Tian, Brigham & Women’s Hosp, Harvard Med. Sch. |
Heart failure is a devastating disease characterized by
left ventricular dysfunction that is associated with a complex of symptoms
that ultimately result in inadequate perfusion of tissues and pulmonary
congestion. Despite the development of novel therapies for the treatment
and prevention of cardiovascular disease the incidence of heart failure is
increasing and each year there are over 1 million hospitalizations for
decompensated heart failure in the United States alone. Clearly, novel
therapeutics are required to treat persons with a number of forms of heart
failure. One major hurdle in our understanding of the pathophysiology of
heart failure is the present lack of precise molecular and cellular
insights into this complex disease process. The advent of gene-targeted
and mutant mouse strains has greatly aided in the elucidation of a number
of cardiovascular disease states. Gene-targeted mice provide an excellent
research tool to investigate the physiological impact of a single gene
mutation in the setting of heart failure. This symposium will focus on
recent physiological research performed using gene-targeted mice in
various models of heart failure. Speakers will present novel information
in murine models of heart failure induced by aortic banding and cardiac
hypertrophy as well as acute myocardial infarction. Speakers will address
important aspects of nitric oxide (NO) derived by eNOS and iNOS and heart
failure. Speakers will address the role of oxidant species in the
pathophysiology of heart failure. Speakers will present highly novel new
data on PDE-5 inhibition and cardiac hypertrophy in heart failure.
Furthermore, speakers will also address the importance of the beta
adrenergic system and heart failure with an emphasis on cell signaling.
This symposium will provide important insights into murine models of heart
failure and also provide new and important information regarding the
molecular and cellular pathophysiology of heart failure. This symposium
is likely to benefit cardiovascular researchers of all backgrounds and
experience levels.
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10:30 AM |
Role of Phosphoinositide 3-kinase and
β-receptor signaling in cardiac function and heart failure.
Howard A. Rockman,
Duke Univ. Sch. of Med.
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11:00 AM |
Phosphodiesterase-5 (PDE-5) inhibition attenuates cardiac hypertrophy and
improves cardiac function in heart failure time.
David A. Kass, Johns Hopkins Univ.
Hosp.
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11:30 AM |
Nitroxyl anion for the treatment of heart
failure.
Nazareno Paolocci, Johns Hopkins Univ.
Sch. of Med.
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12:00 Noon |
Glucose treatment for heart failure?
Rong Tian, Brigham & Women’s Hosp,
Harvard Med. Sch.
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