Control of cardiac contraction by sodium: Promises, reckonings, and new beginnings. (January 2020)

• Record Type: Journal Article
• Authors: Hilgemann, Donald W.
• Is Part Of: Cell calcium. Volume 85(2020)
• Publication Date: 2020-01
• Subjects: Sodium potassium pump -- Sodium calcium exchange -- Local sodium gradient -- Glutathionylation -- Ischemia -- Cardiac excitation contraction coupling -- Simulation -- Sodium gradient -- TRP channels; Calcium -- Metabolism -- Periodicals; Vertebrates -- Physiology -- Periodicals; Calcium -- Physiological effect -- Periodicals; Cell physiology -- Periodicals; Calcium in the body -- Periodicals; 572.516
• DOI: 10.1016/j.ceca.2019.102129
• Languages: English
• ISSNs: 0143-4160

Abstract

Graphical abstract: Highlights: Cardiac contraction is highly dependent on the Na gradient, but it remains enigimatic how the Na gradient is physiologically regulated. Cardiac Na/K pumps may be regulated by small diffusible molecules that remain to be identified. Ca appears to regulate cardiac Na/K pumps via lipid signaling. The existence of local Na gradients in cardiac myocytes is questionable. Abstract: Several generations of cardiac physiologists have verified that basal cardiac contractility depends strongly on the transsarcolemmal Na gradient, and the underlying molecular mechanisms that link cardiac excitation-contraction coupling (ECC) to the Na gradient have been elucidated in good detail for more than 30 years. In brief, small increases of cytoplasmic Na push cardiac (NCX1) Na/Ca exchangers to increase contractility by increasing the myocyte Ca load. Accordingly, basal cardiac contractility is expected to be physiologically regulated by pathways that modify the cardiac Na gradient and the function of Na transporters. Assuming that this expectation is correct, it remains to be elucidated how in detail signaling pathways affecting the cardiac Na gradient are controlled in response to changing cardiac output requirements. Some puzzle pieces that may facilitate progress are outlined in this short review. Key open issues include (1) whether the concept of local Na gradients is viable, (2) how in detail Na channels, Na transporters and Na/K pumps are regulated by lipids and metabolic processes, (3) the physiological roles of Na/K pump inactivation, and (4) the possibility that key diffusible signaling molecules remain to be discovered.