Regular ArticlesQuantitative Analysis of the Expression and Distribution of Calcium Channel α 1 Subunit mRNA in the Atria and Ventricles of the Rat Heart
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MDIMP, a novel cardiac Ca<sup>2+</sup> channel blocker with atrial selectivity
2016, European Journal of PharmacologyCitation Excerpt :Thus, the clinical advantage of MDIMP, if any, might eventually be shown to depend on its possible low levels of toxicity rather than to its potency to inhibit atrial Ca2+channels. It is also important to note that cardiac myocytes primordially express CaV3.1 and CaV1.2 (Larsen et al., 2002). Therefore, further research is needed not only to understand the precise effects of MDIMP on every cloned Ca2+ channel, but also to discover the isoindoline that exhibits the highest specificity for a particular channel.
Direct interaction of Ca<inf>V</inf>β with actin up-regulates l-type calcium currents in HL-1 cardiomyocytes
2015, Journal of Biological ChemistryCitation Excerpt :Nevertheless, inactivation of its gene at adult ages has a moderate effect, suggesting the existence of compensatory mechanisms (3, 16). The association of CaVβ2 with CaV1.2α1, the main LCC in heart (4) increases calcium current density by two different mechanisms: it facilitates the voltage-dependent opening of the channel (15, 17, 18), and it augments the number of channels in the plasma membrane (19). The molecular mechanism by which CaVβ controls the density of channels is the most controversial and least understood (20).
Adenylyl cyclase/cAMP-PKA-mediated phosphorylation of basal L-type Ca<sup>2+</sup> channels in mouse embryonic ventricular myocytes
2011, Cell CalciumCitation Excerpt :Because of the relative paucity of sarcoplasmic reticulum in embryonic cardiocytes, ICa,L contributes proportionally more to the excitation–contraction (EC coupling) in the embryo than in the adult [9,10]. Three different LTCCs, Cav1.1, Cav1.2, and Cav1.3, have been identified in embryonic hearts [11–13]. Among these channels, Cav1.2 is the predominantly expressed isoform in cardiomyocytes [12].
T-type calcium channels in differentiation and proliferation
2006, Cell CalciumRole of T-type Ca<sup>2+</sup> channels in the heart
2006, Cell Calcium
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Please address all correspondence to: Janice Larsen, PhD, University of Illinois, Molecular & Integrative Physiology, 407 South Goodwin Avenue, 524 Burrill Hall, MC-114, Urbana, IL 61801, USA. Tel: 217-244-2940; Fax: 217-333-1133; E-mail: [email protected]