IUPS/APS Newsroom March 29-April 6
San Diego Convention Center
Hall E Registration Area/Flex Unit
Telephone: 619.525.6228
Contact: Donna Krupa
(703) 967-2751 (cell)
(301) 634-7209 (office, outside IUPS dates)
Alcoholism Reduces Male
Heart Muscle’s Ability To Synthesize Protein
Altered
protein factor phosphorylation may point to therapy target
San Diego (April 3, 2005) – The fact that men and women
react differently to alcohol consumption and addiction, health and behavior
risks, disease and death is well known and accepted. Women get drunker
faster on less alcohol than men, but fewer women drink either occasionally
or heavily, and men are more likely to become dependent on alcohol.
However the theories on the cause of those differences
vary widely. Research studies and surveys often yield conflicting results.
The National Institute on Alcohol Abuse and Alcoholism (NIAAA) strategic
plan on health disparities notes that “Chronic alcohol abuse can result in
alcoholic cardiomyopathy (ACM), and there, too disparities appear to exist”
in terms of causes or propensity among different populations.
*Paper presentation: “Gender modulates the
response to chronic alcohol intoxication in the heart,” 12:30 p.m.-3 p.m.
Tuesday April 5, Physiology 909.5 /board #A130. On view 7:30 a.m. - 4 p.m.
Thomas C. Vary is presenting the research at the 35th Congress of
the International Union of Physiological Sciences in San Diego, March 31 -
April 5, 2005.
Alcoholism: Scope of death and overall cost in the
U.S.
ACM is an important cause of mortality among people
suffering from alcoholism. It’s estimated that least 500,000 deaths per year
can be attributed to alcohol abuse in the United States, while as much as
20% of total U.S. health care expenditures in the US may be related to
excessive ethanol consumption in one form or another.
According to a report in the journal “Chest” in the
U.S., “in both sexes and all races, long-term heavy alcohol consumption (of
any beverage type) is the leading cause of a nonischemic, dilated
cardiomyopathy” or ACM. A study in an NIAAA publication reports that the
amount of alcohol necessary to produce the kind of structural and functional
heart abnormalities seen in ACM is “eight or more drinks per day over a
period of 20 years.”
It adds that “the prevalence of ACM is lower in women
than men, yet women may be more vulnerable to ACM,” since some reports say
that ACM develops in women with a lower total lifetime exposure to alcohol.”
Penn State physiologists test role of protein
metabolism, synthesis
Researchers at Pennsylvania State University College of
Medicine’s Cellular and Molecular Physiology Department decided to examine
the metabolic basis of ACM, also called alcoholic heart muscle disease. They
thought “defects in myocardial protein metabolism were probably a
contributing factor for the precipitation and progress of the disease,”
according to Thomas C. Vary, the lead researcher, working with Joseph M.
Leese, an undergraduate summer research fellow and Scot R. Kimball. Changes
in protein metabolism would be expected to influence the expression of
proteins that are needed for normal structure and function in the heart.
Changes in protein expression could lead to structural and/or functional
defects in the heart.
The Penn State researchers decided to compare the
effects of prolonged alcohol consumption on protein metabolism between males
and females in a model of alcoholism. Chronic alcohol consumption was
mimicked by supplying the equivalent of a liter of wine a day in both food
and drinking water. “What we observed was that there were gender
differences in how the heart is able to synthesize proteins both in controls
and alcoholism,” Vary said. “In controls, the ability of the heart muscle
to synthesize proteins was lower in females than in males. Females also had
smaller hearts.”
Male heart muscle protein synthesis declines after
26 weeks of high alcohol use
Moreover “with prolonged alcohol consumption over 26
weeks, the ability of the heart muscle to synthesize proteins was
compromised in males, but not in females,” Vary noted. Going a step further,
they examined “the metabolic pathways involved in protein synthesis.
“We found that one particular step in the process of
protein synthesis was affected in males but not females following prolonged
ethanol consumption,” Vary said. “Furthermore it appeared that the defect
resulted from altered phosphorylation of a particular protein factor
involved in protein synthesis, and the alterations in protein metabolism
mirrored alcohol-induced defects in ventricular function.”
Next steps: Vary said: “Future research will be
directed at developing potential therapeutic modalities that prevent the
alcohol-induced defects in protein synthesis.”
Funding. Research was supported by the National
Institute on Alcohol Abuse & Alcoholism.
***
The 35th Congress of the International Union of
Physiological Sciences is in San Diego, March 31 - April 5, 2005. The
Congress (http://www.iups2005.org/)
is organized by the six member societies of the U.S. National Committee of
the IUPS,
the American Physiological Society,
the Society for Neuroscience,
the Microcirculatory Society,
the Society of General Physiologists,
the Biomedical Engineering Society, and
the Society for Integrative and Comparative Biology, under the auspices
of the U.S. National Academy of Sciences.
The IUPS conference, held every four years, runs
concurrently this year with Experimental Biology 2005 at the San Diego
Convention Center.
The American Physiological Society (APS), which is
hosting IUPS, was founded in 1887 to foster basic and applied science, much
of it relating to human health. The Bethesda, MD-based Society has more than
10,000 members and publishes nearly 4,000 articles every year in its 14
peer-reviewed journals. In May, APS received the Presidential Award
for Excellence in Science, Mathematics and Engineering Mentoring (PAESMEM).
***
Editor’s Note: For further information or to
schedule an interview with a member of the research team, please contact
Donna Krupa at the IUPS/APS newsroom @ 619.525.6228 (March 31-April
6), or (703) 967-2751 (cell) or (301) 634-7209 (office), or Stacy Brooks at
240.432.9697 (cell) or 301.634.7253 (office).
A searchable online program for IUPS and EB is at
http://www.faseb.org/meetings/eb2005/call/default.htm