E
Edward G. Lakatta
Researcher at National Institutes of Health
Publications - 902
Citations - 95504
Edward G. Lakatta is an academic researcher from National Institutes of Health. The author has contributed to research in topics: Blood pressure & Population. The author has an hindex of 146, co-authored 858 publications receiving 88637 citations. Previous affiliations of Edward G. Lakatta include University of Pittsburgh & University College London.
Papers
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Journal ArticleDOI
β-Adrenergic signaling accelerates and synchronizes cardiac ryanodine receptor response to a single L-type Ca2+ channel
Peng Zhou,Yan-Ting Zhao,Yun Bo Guo,Shi Ming Xu,Shu Hua Bai,Edward G. Lakatta,Heping Cheng,Xue Mei Hao,Shi-Qiang Wang +8 more
TL;DR: Results demonstrate unequivocally that RyR activation by a single LCC is accelerated and synchronized during βAR stimulation, and this molecular mechanism of sympathetic regulation will permit more fundamental studies of altered βAR effects in cardiovascular diseases.
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Effects of amiloride on metabolism and contractility during reoxygenation in perfused rat hearts.
TL;DR: To determine whether this dose of amiloride inhibits the manifestations of sodium-mediated calcium gain in the same model during normoxia, the metabolic and functional sequelae of lithium-substituted low sodium (50 mM) perfusion were studied.
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Cytosolic pH measurements in single cardiac myocytes using carboxy-seminaphthorhodafluor-1.
Paul S. Blank,H. S. Silverman,O. Y. Chung,Barbara A. Hogue,Michael D. Stern,Richard G. Hansford,Edward G. Lakatta,Maurizio C. Capogrossi +7 more
TL;DR: C-SNARF-1 can be calibrated in situ using a technique that abolishes all transsarcolemmal pH gradients and the contribution of cellular autofluorescence to the total signal can be made negligible.
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Synchronized Cardiac Impulses Emerge From Heterogeneous Local Calcium Signals Within and Among Cells of Pacemaker Tissue.
Rostislav Bychkov,Magdalena Juhaszova,Kenta Tsutsui,Christopher E. Coletta,Michael D. Stern,Victor A. Maltsev,Edward G. Lakatta +6 more
TL;DR: The study has discovered a novel, microscopic Ca2+ signaling paradigm of SAN operation that has escaped detection using low-resolution, macroscopic tissue isochrones employed in prior studies: synchronized APs emerge from heterogeneous subcellular subthreshold Ca2- signals, resembling multiscale complex processes of impulse generation within clusters of neurons in neuronal networks.