Abstract
Year 2007 is the golden anniversary for the discovery of the sodium- and potassium adenosine triphosphatase, i.e., Na+, K+-ATPase, or Na+-pump by Jens Skou who shared the 1997 Nobel Prize in Chemistry for his discovery. Prior to identification of the enzymatic basis of Na+ and K+ active transport by Skou, the physiological and pharmacological manifestations of such a system had long been evident. Since 1957, there has been a dramatic increase in the knowledge of the physical, chemical, and kinetic properties of the pump and recognition of its basis for a wide range of physiological, pathological, and pharmacological aspects of the cardiovascular system. The Na+-pump has recently been identified as a key partner in a wide array of cell signaling pathways related to hypertrophy and expression of its marker genes. Taken together, these facts make it evident that the pump is a prime target for pharmacological interventions of cardiovascular diseases such as hypertrophy, hypertension, congestive heart failure (CHF), and preeclampsia. This review couples basic attributes of the Na+-pump with pathophysiological etiologies and clinical management of cardiovascular related maladies, and also discusses related patents.
Keywords: Cardiac glycosides, ouabain, marinobufagenin, Na+, K+-ATPase, sodium pump, signal transduction
Recent Patents on Endocrine, Metabolic & Immune Drug Discovery (Discontinued)
Title: The Sodium Pump: Bridging the Basic and Clinical Cardiovascular Sciences
Volume: 1 Issue: 3
Author(s): Donald M. Foster, Suresh K. Verma, Hind Lal, John C. Reneau, Manuela Smith and David E. Dostal
Affiliation:
Keywords: Cardiac glycosides, ouabain, marinobufagenin, Na+, K+-ATPase, sodium pump, signal transduction
Abstract: Year 2007 is the golden anniversary for the discovery of the sodium- and potassium adenosine triphosphatase, i.e., Na+, K+-ATPase, or Na+-pump by Jens Skou who shared the 1997 Nobel Prize in Chemistry for his discovery. Prior to identification of the enzymatic basis of Na+ and K+ active transport by Skou, the physiological and pharmacological manifestations of such a system had long been evident. Since 1957, there has been a dramatic increase in the knowledge of the physical, chemical, and kinetic properties of the pump and recognition of its basis for a wide range of physiological, pathological, and pharmacological aspects of the cardiovascular system. The Na+-pump has recently been identified as a key partner in a wide array of cell signaling pathways related to hypertrophy and expression of its marker genes. Taken together, these facts make it evident that the pump is a prime target for pharmacological interventions of cardiovascular diseases such as hypertrophy, hypertension, congestive heart failure (CHF), and preeclampsia. This review couples basic attributes of the Na+-pump with pathophysiological etiologies and clinical management of cardiovascular related maladies, and also discusses related patents.
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Cite this article as:
Foster M. Donald, Verma K. Suresh, Lal Hind, Reneau C. John, Smith Manuela and Dostal E. David, The Sodium Pump: Bridging the Basic and Clinical Cardiovascular Sciences, Recent Patents on Endocrine, Metabolic & Immune Drug Discovery (Discontinued) 2007; 1 (3) . https://dx.doi.org/10.2174/187221407782409099
DOI https://dx.doi.org/10.2174/187221407782409099 |
Print ISSN 1872-2148 |
Publisher Name Bentham Science Publisher |
Online ISSN 2212-3334 |
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