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Emerging Insights into the Purinergic Signaling in Renal,
Pulmonary and Microvascular Physiology and Pathophysiology
Sponsored by
APS Renal Section
Sunday, April 29 — 8:00-10:00 AM
Washington, DC Convention Center — Room 147B
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| Chaired: |
Bellamkonda K. Kishore, Univ. of Utah
and VAMC Salt Lake City
Edward W. Inscho, Med. Col. of Georgia |
Pharmacological, electrophysiological, functional and
molecular studies have begun to unravel autocrine and/or paracrine
signaling elicited by extracellular nucleotides in the regulation of
glomerular, tubular and microvascular functions in the kidney. In the
lung and airways, similarly elegant studies are establishing the roles
of extracellular nucleotides in the secretion of electrolytes, mucin and
surfactant phospholipids. In recent years rapid progress has been made
in our understanding of the physiology of purinergic signaling as well
as the pathophysiological implications of dysregulated purinergic
signaling in multiple diseases.
For basic scientists and physiologists, this multidisciplinary
symposium presents physiological roles of purinergic signaling in the
following arenas: (1) renal and airway epithelial ion and/or water
transport; (2) the role of ductal epithelial cell’s apical central cilium in
flow response and purinergic signaling; (3) luminal receptors for locally
released mediators within microenvironments; and (4) interactions of
purinergics with prostanoids and vasopressin in the collecting duct water
and sodium absorption. For clinical scientists interested in pathophysiology,
this symposium presents emerging concepts on the role of purinergic
signaling in diverse disease conditions. These include: (1) alterations that
occur in renal hemodynamics, autoregulatory responses, and microvascular
smooth muscle signaling in hypertension; (2) pathophysiology of polycystic
kidney disease (PKD) and the etiology of severe hypertension in ARPKD; (3)
role of purinergic signaling in water balance disorders and
vasopressin-excess states, and in acquired nephrogenic diabetes insipidus;
and (4) dysregulation of salt and chloride transport in cystic fibrosis.
Concepts and information generated by experimentation at
multiple levels using multiple approaches that address key issues in
purinergic physiology and pathophysiology will be presented. Furthermore,
this symposium will present future directions in purinergic research, such
as development of specific agonists and/or antagonists to receptors,
specific inhibitors of ecto-nucleotidases, or scavengers of extracellular
nucleotides, for therapeutic modulation of purinergic signaling in specific
disease conditions.
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8:00 AM |
Autocrine regulation by locally released
purinergics: physiology, pathophysiology, and translational
implications.
Erik M. Schwiebert, Univ. of Alabama at Birmingham
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8:30 AM |
Modification of renal microvascular purinergic
signaling in hypertension.
Edward W. Inscho, Med. Col. of Georgia
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9:00 AM |
The flow response in the renal tubule: a
purinergic issue.
Helle Prætorius, Univ. of Aarhus
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9:30 AM |
Interaction of purinergics with prostanoids and
vasopressin in the collecting duct: physiology and pathophysiology.
Bellamkonda K. Kishore, Univ. of Utah and VAMC Med. Ctr.,
Salt Lake City
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