Although the atrial natriuretic polypeptide (ANP) hormone
secreted by atria plays a major role in the medically important
function of fluid, electrolyte, and blood pressure homeostasis, the
cellular mechanisms by which stretching atria stimulates hormone
secretion are unknown. The long-term goal of this proposal is to
investigate the mechanisms of stretch-secretion coupling in atria
and its interaction with atrial contraction by studying in detail
the Ca2+-sensitive mechanotransducer relationship between
stretch-activated atrial ion transport and ANP secretion
demonstrable in intact rat atria. The relationship will be
examined (a) by in vitro studies on intact atria stretched by a
physiological range of distending pressures in which stretch-
activated cellular net Na efflux, Ca influx, depolarization, and
ANP secretion can be measured together during variations of
passive stretch and contraction frequency while conditions
determining Ca2+ influx across the plasma membrane or Ca2+
release from sarcoplasmic reticulum (SR) can be separately
varied; (b) by single channel patch-clamp studies on cultured and
freshly dissociated cardiac myocytes to identify and characterize
stretch-activated channels and/or second messenger systems; (c)
by applying fura-2 fluorescence microscopy interfaced with
digital computer-aided image analysis to single atrial myocytes
(both cultured myocytes and freshly dissociated myocytes) to
investigate the time course and subcellular localization of the
changes in cytoplasmic Ca2+ associated with changes in ANP
secretion due to variations in ionic environment, membrane
stretch, contraction rate, activation or inhibition of second
messenger systems, and other variables; (d) by correlating
stretch-activated ANP secretion with stretch-activated changes
in tension and in plasmalemmal Na-Ca exchange using
measurements of tension and intracellular Na+ activity in
quiescent and contracting rat atrial trabeculae; and (e) by
correlating ANP secretion rates of atrial myocytes cultured from
adult rats with observations of microtubule-associated
cytoplasmic translocation of atrial granules from the Golgi to the
plasma membrane using electron microscopy and double
immunofluorescence microscopy while stretch, Ca influx, and SR
Ca release can be separately varied and second messenger
systems can be stimulated or blocked in different ways.
No Sub Projects information available for 5R37HL010503-25
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
No Publications available for 5R37HL010503-25
Patents
No Patents information available for 5R37HL010503-25
Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
No Outcomes available for 5R37HL010503-25
Clinical Studies
No Clinical Studies information available for 5R37HL010503-25
News and More
Related News Releases
No news release information available for 5R37HL010503-25
History
No Historical information available for 5R37HL010503-25
Similar Projects
No Similar Projects information available for 5R37HL010503-25