• Medientyp: E-Book
  • Titel: Voltage-gated Ca2+ Channels: Pharmacology, Modulation and their Role in Human Disease
  • Beteiligte: Striessnig, Jörg [Herausgeber:in]
  • Erschienen: Cham: Springer International Publishing, 2023.
    Cham: Imprint: Springer, 2023.
  • Erschienen in: Handbook of Experimental Pharmacology ; 279
  • Ausgabe: 1st ed. 2023.
  • Umfang: 1 Online-Ressource(XII, 316 p. 100 illus., 30 illus. in color.)
  • Sprache: Englisch
  • DOI: 10.1007/978-3-031-38437-0
  • ISBN: 9783031384370
  • Identifikator:
  • Schlagwörter: Pharmacology. ; Medical genetics. ; Human physiology.
  • Entstehung:
  • Anmerkungen:
  • Beschreibung: Preface -- Part 1 Modulation -- Cav1.1Calcium Channel Signaling Complexes in Excitation–Contraction Coupling: Insights from Channelopathies -- Mechanisms of Vascular CaV1.2 Channel Regulation During Diabetic Hyperglycemia -- Sympathetic Nervous System Regulation of Cardiac Calcium Channels -- Modulation of CaV1.2 Channel Function by Interacting Proteins and Post-Translational Modifications: Implications in Cardiovascular Diseases and COVID-19 -- Part 2 Pharmacological Approaches -- Pathophysiological Roles of Auxiliary Calcium Channel α2δ Subunits -- Design and Applications of Genetically-Encoded Voltage-Dependent Calcium Channel Inhibitors -- Part 3 Disease insight from channelopathies: consequences for pharmacology and therapeutic strategies -- CACNA1C-Related Channelopathies -- CACNA1D-Related Channelopathies: From Hypertension to Autism -- CACNA1A-Related Channelopathies: Clinical Manifestations and Treatment Options -- CaV3.2 (CACNA1H) in Primary Aldosteronism,- CaV3.3 Channelopathies -- Pathophysiological Roles of Auxiliary Calcium Channel α2δ Subunits.

    The aim of this volume is to summarize novel findings on the function, pathophysiology, and regulation of voltage-gated Ca2+ channels and on novel concepts of their pharmacological modulation. Impressive insights into the role of channel function and regulation have come from Ca2+ channelopathies affecting the pore-forming as well as accessory subunits and channel-interacting proteins. Moreover, the long-sought molecular basis for key regulatory pathways have been discovered as well as exciting concepts of their subtype-selective pharmacological modulation.