Abstract
1. The passive and active electrical properties of pregnant rat single myometrial cells in short-term primary culture were analysed using a single-electrode voltage or current clamp. 2. Action potentials and membrane currents were recorded in the presence of tetraethylammonium chloride and 4-aminopyridine (10 mM each) and with Cs+ solution (4 M) in the microelectrode. 3. The voltage dependence, the action of Ca2+ antagonists and the effects of Sr2+ or Ba2+ substitution were studied. The peak Ca2+ current density was in the range 15-20 microA/cm2 in 10 mM-Ca2+ solution. 4. According to both measurement of the reversal potential of Ca2+ channel currents and comparison of the inward currents after correction for changing surface charge, the relative selectivity sequence of the Ca2+ channel for divalent cations was Ca2+ greater than Sr2+ = Ba2+. 5. The decay of Ca2+ channel current during a maintained depolarization was slowed when external Ca2+ was replaced by Sr2+ or Ba2+. The decay reflected an inactivation of Ca2+ channel conductance, as assessed by the decreased amplitude of inward tail currents following progressively longer depolarizations and the stable value of the reversal potential when Ca2+ channel current was increased during conditioning pulses. 6. Voltage-dependent inactivation was illustrated by inactivation of outward Ca2+ channel current due to K+ and/or Cs+ efflux with external Ba2+ or in the absence of any permeant divalent cation. 7. The relationship between inactivation and the intracellular Ca2+ concentration was assessed by a double-pulse method. Conditioning pulses that produced maximal Ca2+ current induced maximal inactivation; with stronger depolarizations, inactivation decreased but was not completely prevented at the expected Ca2+ reversal potential. Increasing the amount of Ca2+ entering the cell during the pre-pulse reduced both amplitude and kinetics of test Ca2+ currents. These results were not observed with Ba2+ as the charge carrier. 8. Ca2+ channel current inactivation was best fitted by a two-exponential function. The fast time constant of inactivation was larger in Ba2+ solution than in Ca2+ solution but both time constants showed little variation with membrane potential. The slow time constants of inactivation were steeply voltage dependent.(ABSTRACT TRUNCATED AT 400 WORDS)
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- Abe Y., Tomita T. Cable properties of smooth muscle. J Physiol. 1968 May;196(1):87–100. doi: 10.1113/jphysiol.1968.sp008496. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Amédée T., Mironneau C., Mironneau J. Isolation and contractile responses of single pregnant rat myometrial cells in short-term primary culture and the effects of pharmacological and electrical stimuli. Br J Pharmacol. 1986 Aug;88(4):873–880. doi: 10.1111/j.1476-5381.1986.tb16261.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bean B. P., Sturek M., Puga A., Hermsmeyer K. Calcium channels in muscle cells isolated from rat mesenteric arteries: modulation by dihydropyridine drugs. Circ Res. 1986 Aug;59(2):229–235. doi: 10.1161/01.res.59.2.229. [DOI] [PubMed] [Google Scholar]
- Bean B. P. Two kinds of calcium channels in canine atrial cells. Differences in kinetics, selectivity, and pharmacology. J Gen Physiol. 1985 Jul;86(1):1–30. doi: 10.1085/jgp.86.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bolton T. B., Lang R. J., Takewaki T., Benham C. D. Patch and whole-cell voltage clamp of single mammalian visceral and vascular smooth muscle cells. Experientia. 1985 Jul 15;41(7):887–894. doi: 10.1007/BF01970006. [DOI] [PubMed] [Google Scholar]
- Brown A. M., Morimoto K., Tsuda Y., wilson D. L. Calcium current-dependent and voltage-dependent inactivation of calcium channels in Helix aspersa. J Physiol. 1981 Nov;320:193–218. doi: 10.1113/jphysiol.1981.sp013944. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Byerly L., Chase P. B., Stimers J. R. Permeation and interaction of divalent cations in calcium channels of snail neurons. J Gen Physiol. 1985 Apr;85(4):491–518. doi: 10.1085/jgp.85.4.491. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Carbone E., Lux H. D. A low voltage-activated calcium conductance in embryonic chick sensory neurons. Biophys J. 1984 Sep;46(3):413–418. doi: 10.1016/S0006-3495(84)84037-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cognard C., Lazdunski M., Romey G. Different types of Ca2+ channels in mammalian skeletal muscle cells in culture. Proc Natl Acad Sci U S A. 1986 Jan;83(2):517–521. doi: 10.1073/pnas.83.2.517. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Eckert R., Chad J. E. Inactivation of Ca channels. Prog Biophys Mol Biol. 1984;44(3):215–267. doi: 10.1016/0079-6107(84)90009-9. [DOI] [PubMed] [Google Scholar]
- FRANKENHAEUSER B., HODGKIN A. L. The action of calcium on the electrical properties of squid axons. J Physiol. 1957 Jul 11;137(2):218–244. doi: 10.1113/jphysiol.1957.sp005808. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Friedman M. E., Suarez-Kurtz G., Kaczorowski G. J., Katz G. M., Reuben J. P. Two calcium currents in a smooth muscle cell line. Am J Physiol. 1986 Apr;250(4 Pt 2):H699–H703. doi: 10.1152/ajpheart.1986.250.4.H699. [DOI] [PubMed] [Google Scholar]
- Fromm M., Schultz S. G. Some properties of KCl-filled microelectrodes: correlation of potassium "leakage" with tip resistance. J Membr Biol. 1981;62(3):239–244. doi: 10.1007/BF01998169. [DOI] [PubMed] [Google Scholar]
- Fukushima Y., Hagiwara S. Currents carried by monovalent cations through calcium channels in mouse neoplastic B lymphocytes. J Physiol. 1985 Jan;358:255–284. doi: 10.1113/jphysiol.1985.sp015550. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hagiwara S., Byerly L. Calcium channel. Annu Rev Neurosci. 1981;4:69–125. doi: 10.1146/annurev.ne.04.030181.000441. [DOI] [PubMed] [Google Scholar]
- Hess P., Lansman J. B., Tsien R. W. Calcium channel selectivity for divalent and monovalent cations. Voltage and concentration dependence of single channel current in ventricular heart cells. J Gen Physiol. 1986 Sep;88(3):293–319. doi: 10.1085/jgp.88.3.293. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jmari K., Mironneau C., Mironneau J. Inactivation of calcium channel current in rat uterine smooth muscle: evidence for calcium- and voltage-mediated mechanisms. J Physiol. 1986 Nov;380:111–126. doi: 10.1113/jphysiol.1986.sp016275. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jmari K., Mironneau C., Mironneau J. Selectivity of calcium channels in rat uterine smooth muscle: interactions between sodium, calcium and barium ions. J Physiol. 1987 Mar;384:247–261. doi: 10.1113/jphysiol.1987.sp016453. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kass R. S., Sanguinetti M. C. Inactivation of calcium channel current in the calf cardiac Purkinje fiber. Evidence for voltage- and calcium-mediated mechanisms. J Gen Physiol. 1984 Nov;84(5):705–726. doi: 10.1085/jgp.84.5.705. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lee K. S., Marban E., Tsien R. W. Inactivation of calcium channels in mammalian heart cells: joint dependence on membrane potential and intracellular calcium. J Physiol. 1985 Jul;364:395–411. doi: 10.1113/jphysiol.1985.sp015752. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lee K. S., Tsien R. W. High selectivity of calcium channels in single dialysed heart cells of the guinea-pig. J Physiol. 1984 Sep;354:253–272. doi: 10.1113/jphysiol.1984.sp015374. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Loirand G., Pacaud P., Mironneau C., Mironneau J. Evidence for two distinct calcium channels in rat vascular smooth muscle cells in short-term primary culture. Pflugers Arch. 1986 Nov;407(5):566–568. doi: 10.1007/BF00657519. [DOI] [PubMed] [Google Scholar]
- Mentrard D., Vassort G., Fischmeister R. Calcium-mediated inactivation of the calcium conductance in cesium-loaded frog heart cells. J Gen Physiol. 1984 Jan;83(1):105–131. doi: 10.1085/jgp.83.1.105. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mironneau J., Eugene D., Mironneau C. Sodium action potentials induced by calcium chelation in rat uterine smooth muscle. Pflugers Arch. 1982 Nov 11;395(3):232–238. doi: 10.1007/BF00584815. [DOI] [PubMed] [Google Scholar]
- Mironneau J., Savineau J. P., Mironneau C. Fast outward current controlling electrical activity in rat uterine smooth muscle during gestation. J Physiol (Paris) 1981 Mar;77(8):851–859. [PubMed] [Google Scholar]
- Nowycky M. C., Fox A. P., Tsien R. W. Three types of neuronal calcium channel with different calcium agonist sensitivity. Nature. 1985 Aug 1;316(6027):440–443. doi: 10.1038/316440a0. [DOI] [PubMed] [Google Scholar]
- Sturek M., Hermsmeyer K. Calcium and sodium channels in spontaneously contracting vascular muscle cells. Science. 1986 Jul 25;233(4762):475–478. doi: 10.1126/science.2425434. [DOI] [PubMed] [Google Scholar]
- Worley J. F., 3rd, Deitmer J. W., Nelson M. T. Single nisoldipine-sensitive calcium channels in smooth muscle cells isolated from rabbit mesenteric artery. Proc Natl Acad Sci U S A. 1986 Aug;83(15):5746–5750. doi: 10.1073/pnas.83.15.5746. [DOI] [PMC free article] [PubMed] [Google Scholar]