001     283125
005     20260105095153.0
024 7 _ |a 10.1161/CIRCRESAHA.125.327497
|2 doi
024 7 _ |a pmid:41342134
|2 pmid
024 7 _ |a pmc:PMC12757128
|2 pmc
024 7 _ |a 0009-7330
|2 ISSN
024 7 _ |a 1524-4571
|2 ISSN
037 _ _ |a DZNE-2026-00021
041 _ _ |a English
082 _ _ |a 610
100 1 _ |a Torre, Eleonora
|0 0000-0003-1822-8495
|b 0
245 _ _ |a L-Type Cav1.3 and HCN Channels Mediate Heart Rate Acceleration by Catecholamines.
260 _ _ |a New York, NY
|c 2026
|b Assoc.
336 7 _ |a article
|2 DRIVER
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|b journal
|m journal
|0 PUB:(DE-HGF)16
|s 1767603009_32745
|2 PUB:(DE-HGF)
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a Journal Article
|0 0
|2 EndNote
520 _ _ |a The ionic mechanism by which catecholamines increase the heart rate is incompletely understood. In this study, we have assessed the roles of sinoatrial node L-type Cav1.3 (α1D) Ca2+ channels, phosphorylation of L-type channel regulatory partner protein Rad (Ras-related RGK GTP-binding protein), and cAMP-dependent regulation of hyperpolarization-activated HCN (hyperpolarization-activated cyclic nucleotide-gated) channels.We studied β-adrenergic regulation of heart rate and sinoatrial pacemaker activity in mice lacking Cav1.3 channels and in mice expressing dihydropyridine-insensitive L-type Cav1.2 channels alone or concomitantly expressing cAMP-insensitive HCN4 subunits in a heart-specific and time-controlled manner. We also studied the chronotropic response to sympathomimetics of sinoatrial pacemaker myocytes under conditions of specific inhibition of cAMP-dependent regulation of HCN4 by the cyclic dinucleotide cyclic di-(3',5')-GMP and ablation of PKA (protein kinase A)-dependent phosphorylation of Rad.Mutant mice with knockout of Cav1.3 and cAMP-insensitive HCN4 subunits in the heart lacked diurnal variation in heart rate and failed to increase their heart rate after administration of catecholamines or during physical activity. Selective pharmacological inhibition of Cav1.3 prevented the enhancement of pacemaker activity by sympathomimetics or by direct activation of adenylate cyclase, as well as by phosphodiesterase inhibitors, when cAMP-dependent regulation of HCN was simultaneously silenced. Upregulation of Cav1.3 and HCN-mediated funny current (If) accounted for the total change in diastolic current on activation of β-adrenoceptors, explaining the loss of chronotropic effect of catecholamines. Preventing PKA phosphorylation of Rad abrogated the chronotropic response to sympathomimetics of intact hearts under HCN blockade, or in pacemaker myocytes on preventing cAMP-dependent regulation of HCN4, respectively.PKA phosphorylation of Rad, which disinhibits Cav1.3 channels and cAMP-dependent activation of HCN channels, are key effectors in β-adrenergic regulation of cardiac pacemaker activity and can sustain positive chronotropic effects independently. These findings on Rad-mediated regulation of Cav1.3 and HCN channels unravel the ionic mechanisms underlying the catecholaminergic acceleration of the heart rate.
536 _ _ |a 351 - Brain Function (POF4-351)
|0 G:(DE-HGF)POF4-351
|c POF4-351
|f POF IV
|x 0
588 _ _ |a Dataset connected to CrossRef, PubMed, , Journals: pub.dzne.de
650 _ 7 |a catecholamines
|2 Other
650 _ 7 |a heart rate
|2 Other
650 _ 7 |a phosphorylation
|2 Other
650 _ 7 |a sinoatrial node
|2 Other
650 _ 7 |a sympathomimetics
|2 Other
650 _ 7 |a Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels
|2 NLM Chemicals
650 _ 7 |a Calcium Channels, L-Type
|2 NLM Chemicals
650 _ 7 |a Catecholamines
|2 NLM Chemicals
650 _ 7 |a Cyclic AMP-Dependent Protein Kinases
|0 EC 2.7.11.11
|2 NLM Chemicals
650 _ 7 |a Cyclic AMP
|0 E0399OZS9N
|2 NLM Chemicals
650 _ 7 |a Hcn4 protein, mouse
|2 NLM Chemicals
650 _ 7 |a Rrad protein, mouse
|2 NLM Chemicals
650 _ 7 |a Muscle Proteins
|2 NLM Chemicals
650 _ 7 |a Adrenergic beta-Agonists
|2 NLM Chemicals
650 _ 7 |a ras Proteins
|0 EC 3.6.5.2
|2 NLM Chemicals
650 _ 2 |a Animals
|2 MeSH
650 _ 2 |a Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels: metabolism
|2 MeSH
650 _ 2 |a Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels: genetics
|2 MeSH
650 _ 2 |a Heart Rate: drug effects
|2 MeSH
650 _ 2 |a Heart Rate: physiology
|2 MeSH
650 _ 2 |a Mice
|2 MeSH
650 _ 2 |a Calcium Channels, L-Type: genetics
|2 MeSH
650 _ 2 |a Calcium Channels, L-Type: metabolism
|2 MeSH
650 _ 2 |a Calcium Channels, L-Type: deficiency
|2 MeSH
650 _ 2 |a Calcium Channels, L-Type: physiology
|2 MeSH
650 _ 2 |a Phosphorylation
|2 MeSH
650 _ 2 |a Catecholamines: pharmacology
|2 MeSH
650 _ 2 |a Catecholamines: metabolism
|2 MeSH
650 _ 2 |a Sinoatrial Node: drug effects
|2 MeSH
650 _ 2 |a Sinoatrial Node: metabolism
|2 MeSH
650 _ 2 |a Sinoatrial Node: physiology
|2 MeSH
650 _ 2 |a Sinoatrial Node: cytology
|2 MeSH
650 _ 2 |a Mice, Knockout
|2 MeSH
650 _ 2 |a Cyclic AMP-Dependent Protein Kinases: metabolism
|2 MeSH
650 _ 2 |a Cyclic AMP: metabolism
|2 MeSH
650 _ 2 |a Myocytes, Cardiac: drug effects
|2 MeSH
650 _ 2 |a Myocytes, Cardiac: metabolism
|2 MeSH
650 _ 2 |a Mice, Inbred C57BL
|2 MeSH
650 _ 2 |a Male
|2 MeSH
650 _ 2 |a Muscle Proteins: metabolism
|2 MeSH
650 _ 2 |a Adrenergic beta-Agonists: pharmacology
|2 MeSH
650 _ 2 |a ras Proteins
|2 MeSH
700 1 _ |a Faure, Mélanie
|b 1
700 1 _ |a Bidaud, Isabelle
|0 0000-0002-1812-1447
|b 2
700 1 _ |a Baudot, Matthias
|0 0000-0002-8725-3048
|b 3
700 1 _ |a Gaillardon, Marvin
|b 4
700 1 _ |a Pereira de Vasconcelos, Walma
|0 0009-0000-2471-8445
|b 5
700 1 _ |a Laarioui, Sihame
|0 0009-0009-4852-371X
|b 6
700 1 _ |a Talssi, Leïla
|b 7
700 1 _ |a Engeland, Birgit
|0 P:(DE-2719)2810970
|b 8
700 1 _ |a Reiken, Steven
|0 0000-0002-5807-3574
|b 9
700 1 _ |a Saponaro, Andrea
|0 0000-0001-5035-5174
|b 10
700 1 _ |a Chen, Bi-Xing
|b 11
700 1 _ |a Moroni, Anna
|0 0000-0002-1860-406X
|b 12
700 1 _ |a D'Souza, Alicia
|0 0000-0002-9700-5523
|b 13
700 1 _ |a Isbrandt, Dirk
|0 P:(DE-2719)2810976
|b 14
700 1 _ |a Marks, Andrew R
|0 0000-0002-8057-1502
|b 15
700 1 _ |a Marx, Steven O
|0 0000-0002-0577-6030
|b 16
700 1 _ |a Mesirca, Pietro
|0 0000-0002-9538-3096
|b 17
700 1 _ |a Mangoni, Matteo E
|0 0000-0002-8892-3373
|b 18
773 _ _ |a 10.1161/CIRCRESAHA.125.327497
|g Vol. 138, no. 1
|0 PERI:(DE-600)1467838-X
|n 1
|p e327497
|t Circulation research
|v 138
|y 2026
|x 0009-7330
856 4 _ |u https://pub.dzne.de/record/283125/files/DZNE-2026-00021.pdf
|y Restricted
856 4 _ |u https://pub.dzne.de/record/283125/files/DZNE-2026-00021.pdf?subformat=pdfa
|x pdfa
|y Restricted
910 1 _ |a Deutsches Zentrum für Neurodegenerative Erkrankungen
|0 I:(DE-588)1065079516
|k DZNE
|b 8
|6 P:(DE-2719)2810970
910 1 _ |a Deutsches Zentrum für Neurodegenerative Erkrankungen
|0 I:(DE-588)1065079516
|k DZNE
|b 14
|6 P:(DE-2719)2810976
913 1 _ |a DE-HGF
|b Gesundheit
|l Neurodegenerative Diseases
|1 G:(DE-HGF)POF4-350
|0 G:(DE-HGF)POF4-351
|3 G:(DE-HGF)POF4
|2 G:(DE-HGF)POF4-300
|4 G:(DE-HGF)POF
|v Brain Function
|x 0
915 _ _ |a Allianz-Lizenz
|0 StatID:(DE-HGF)0410
|2 StatID
|d 2024-12-13
|w ger
915 _ _ |a JCR
|0 StatID:(DE-HGF)0100
|2 StatID
|b CIRC RES : 2022
|d 2024-12-13
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0200
|2 StatID
|b SCOPUS
|d 2024-12-13
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0300
|2 StatID
|b Medline
|d 2024-12-13
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0199
|2 StatID
|b Clarivate Analytics Master Journal List
|d 2024-12-13
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1050
|2 StatID
|b BIOSIS Previews
|d 2024-12-13
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0160
|2 StatID
|b Essential Science Indicators
|d 2024-12-13
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1030
|2 StatID
|b Current Contents - Life Sciences
|d 2024-12-13
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1190
|2 StatID
|b Biological Abstracts
|d 2024-12-13
915 _ _ |a WoS
|0 StatID:(DE-HGF)0113
|2 StatID
|b Science Citation Index Expanded
|d 2024-12-13
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0150
|2 StatID
|b Web of Science Core Collection
|d 2024-12-13
915 _ _ |a IF >= 20
|0 StatID:(DE-HGF)9920
|2 StatID
|b CIRC RES : 2022
|d 2024-12-13
920 1 _ |0 I:(DE-2719)1011003
|k AG Isbrandt
|l Experimental Neurophysiology
|x 0
980 _ _ |a journal
980 _ _ |a EDITORS
980 _ _ |a VDBINPRINT
980 _ _ |a I:(DE-2719)1011003
980 _ _ |a UNRESTRICTED


LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21