Literature DB >> 2558173

Low-voltage-activated calcium current in rat aorta smooth muscle cells in primary culture.

N Akaike1, H Kanaide, T Kuga, M Nakamura, J Sadoshima, H Tomoike.   

Abstract

1. Electrical and pharmacological properties of the low-voltage-activated Ca2+ current (ICa, LVA) in rat aorta smooth muscle cells (SMC) in primary culture were examined, particularly in comparison with the high-voltage-activated Ca2+ current (ICa, HVA). Both types of Ca2+ currents were recorded in external solution containing 20 mM-Ca2+, using the whole-cell voltage-clamp technique. 2. ICa, LVA was evoked by step depolarizations to potentials more positive than -60 mV from a holding potential of -100 mV, and reached a peak in the current-voltage (I-V) relationship around -30 mV. ICa, HVA was activated at -20 mV, and reached a peak at +20 mV. 3. The intracellular dialysis of 5 mM-F- irreversibly suppressed ICa, HVA, with time, while it has little effect on the ICa, LVA. The ICa, LVA could be separated from the ICa, HVA by either selecting the holding and test potential levels or by perfusing intracellularly with F-. 4. The ratio of peak amplitude of Ba2+, Sr2+ and Ca2+ currents in the respective I-V relationship was 1.6:1.2:1.0 for high-voltage-activated Ca2+ channels and was 1.0:1.4:1.0 for low-voltage-activated ones. 5. The inactivation phase of ICa, HVA was fitted by a sum of double-exponential functions, the time constants of which were larger when the current was carried by Ba2+ than by Ca2+. The inactivation time course of ICa, LVA was fitted by a single-exponential function, and the time constant was practically the same when the current was carried by Ba2+ or by Ca2+. Activation and inactivation processes of ICa, LVA were potential-dependent. 6. The steady-state inactivation curve of ICa, LVA was fitted by the Boltzmann equation, having a mid-potential of -80 mV and a slope factor of 5.0. The recovery time course from steady-state inactivation was fitted by a sum of two exponential functions. The time constants of the faster phase were 230 and 380 ms, and those of slower phase were 2.8 and 1.8 s at the repolarization potentials of -120 and -100 mV, respectively. 7. The amplitude of ICa, LVA depended on the external Ca2+ concentration ([Ca2+]o), approaching saturation at 95 mM [Ca2+]o. 8. Various polyvalent cations blocked both types of Ca2+ current reversibly in the order (IC50 in M): La3+ (8 x 10(-8)) greater than Cd2+ (6 x 10(-6)) greater than Ni2+ (1 x 10(-5)) greater than Zn2+ (2 x 10(-5)) for ICa, HVA, and La3+ (6 x 10(-7)) greater than Zn2+ (3 x 10(-5)) greater than Cd2+ (4 x 10(-4)) greater than Ni2+ (6 x 10(-4)) for ICa, LVA.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1989        PMID: 2558173      PMCID: PMC1189208          DOI: 10.1113/jphysiol.1989.sp017754

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  34 in total

1.  A low threshold calcium current recorded at physiological Ca concentrations in single frog atrial cells.

Authors:  R Bonvallet
Journal:  Pflugers Arch       Date:  1987-05       Impact factor: 3.657

2.  Whole-cell and single-channel calcium currents of isolated smooth muscle cells from saphenous vein.

Authors:  A Yatani; C L Seidel; J Allen; A M Brown
Journal:  Circ Res       Date:  1987-04       Impact factor: 17.367

3.  Evidence for two distinct calcium channels in rat vascular smooth muscle cells in short-term primary culture.

Authors:  G Loirand; P Pacaud; C Mironneau; J Mironneau
Journal:  Pflugers Arch       Date:  1986-11       Impact factor: 3.657

4.  Single nisoldipine-sensitive calcium channels in smooth muscle cells isolated from rabbit mesenteric artery.

Authors:  J F Worley; J W Deitmer; M T Nelson
Journal:  Proc Natl Acad Sci U S A       Date:  1986-08       Impact factor: 11.205

5.  Calcium and sodium channels in spontaneously contracting vascular muscle cells.

Authors:  M Sturek; K Hermsmeyer
Journal:  Science       Date:  1986-07-25       Impact factor: 47.728

6.  Calcium channels in muscle cells isolated from rat mesenteric arteries: modulation by dihydropyridine drugs.

Authors:  B P Bean; M Sturek; A Puga; K Hermsmeyer
Journal:  Circ Res       Date:  1986-08       Impact factor: 17.367

7.  Actions of flunarizine, a Ca++ antagonist, on ionic currents in fragmented smooth muscle cells of the rabbit small intestine.

Authors:  K Terada; Y Ohya; K Kitamura; H Kuriyama
Journal:  J Pharmacol Exp Ther       Date:  1987-03       Impact factor: 4.030

8.  Calcium current-dependent and voltage-dependent inactivation of calcium channels in Helix aspersa.

Authors:  A M Brown; K Morimoto; Y Tsuda; D L wilson
Journal:  J Physiol       Date:  1981-11       Impact factor: 5.182

9.  Mechanism of calcium channel blockade by verapamil, D600, diltiazem and nitrendipine in single dialysed heart cells.

Authors:  K S Lee; R W Tsien
Journal:  Nature       Date:  1983-04-28       Impact factor: 49.962

10.  Development of two types of calcium channels in cultured mammalian hippocampal neurons.

Authors:  Y Yaari; B Hamon; H D Lux
Journal:  Science       Date:  1987-02-06       Impact factor: 47.728

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  29 in total

1.  Zinc-induced changes in ionic currents of clonal rat pancreatic -cells: activation of ATP-sensitive K+ channels.

Authors:  A Bloc; T Cens; H Cruz; Y Dunant
Journal:  J Physiol       Date:  2000-12-15       Impact factor: 5.182

2.  Ca2+ transport properties and determinants of anomalous mole fraction effects of single voltage-gated Ca2+ channels in hair cells from bullfrog saccule.

Authors:  Adrian Rodriguez-Contreras; Wolfgang Nonner; Ebenezer N Yamoah
Journal:  J Physiol       Date:  2002-02-01       Impact factor: 5.182

3.  Control of the low voltage-activated calcium channel of mouse sperm by egg ZP3 and by membrane hyperpolarization during capacitation.

Authors:  C Arnoult; I G Kazam; P E Visconti; G S Kopf; M Villaz; H M Florman
Journal:  Proc Natl Acad Sci U S A       Date:  1999-06-08       Impact factor: 11.205

Review 4.  Low-voltage-activated ("T-Type") calcium channels in review.

Authors:  Anne Marie R Yunker; Maureen W McEnery
Journal:  J Bioenerg Biomembr       Date:  2003-12       Impact factor: 2.945

Review 5.  Modulation and pharmacology of low voltage-activated ("T-Type") calcium channels.

Authors:  Anne Marie R Yunker
Journal:  J Bioenerg Biomembr       Date:  2003-12       Impact factor: 2.945

6.  Stimulation-induced potentiation of T-type Ca2+ channel currents in myocytes from guinea-pig coronary artery.

Authors:  G Isenberg
Journal:  J Physiol       Date:  1991-11       Impact factor: 5.182

7.  Calcium channel currents in isolated smooth muscle cells from the basilar artery of the guinea pig.

Authors:  J M Simard
Journal:  Pflugers Arch       Date:  1991-01       Impact factor: 3.657

Review 8.  Calcium Channels in Vascular Smooth Muscle.

Authors:  D Ghosh; A U Syed; M P Prada; M A Nystoriak; L F Santana; M Nieves-Cintrón; M F Navedo
Journal:  Adv Pharmacol       Date:  2016-10-14

Review 9.  Molecular characterization of a novel family of low voltage-activated, T-type, calcium channels.

Authors:  E Perez-Reyes
Journal:  J Bioenerg Biomembr       Date:  1998-08       Impact factor: 2.945

10.  Two high-voltage-activated, dihydropyridine-sensitive Ca2+ channel currents with distinct electrophysiological and pharmacological properties in cultured rat aortic myocytes.

Authors:  D Neveu; J Nargeot; S Richard
Journal:  Pflugers Arch       Date:  1993-06       Impact factor: 3.657

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