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. 1992 Sep;107(1):134–140. doi: 10.1111/j.1476-5381.1992.tb14475.x

Cyclopiazonic acid, an inhibitor of the sarcoplasmic reticulum Ca(2+)-pump, reduces Ca(2+)-dependent K+ currents in guinea-pig smooth muscle cells.

M Suzuki 1, K Muraki 1, Y Imaizumi 1, M Watanabe 1
PMCID: PMC1907594  PMID: 1330156

Abstract

1. Effects of cyclopiazonic acid (CPA), a specific inhibitor of the Ca(2+)-ATPase in sarcoplasmic reticulum (SR), on membrane ionic currents were examined in single smooth muscle cells freshly isolated from ileal longitudinal strips and urinary bladder of the guinea-pig. 2. Under whole-cell clamp, CPA (1-10 microM) reduced peak outward current elicited by depolarization in a concentration-dependent manner. The concentration of CPA required for 50% decrease in the peak outward current was approximately 3 microM in ileal cells under these conditions. The current reduced by CPA recovered by more than 70% after washout. 3. The transient outward current elicited by application of 5 mM caffeine at a holding potential of -50 mV in Ca2+ free solution was almost abolished, when the preceding Ca(2+)-loading of the cell in a solution containing 2.2 mM Ca2+ was performed in the presence of 3 microM CPA. 4. When the Ca(2+)-dependent K+ current (IK-Ca) and Ca2+ current (ICa) were inhibited by addition of Ca2+, the remaining delayed rectifier type K+ current was not affected by 10 microM CPA. When outward currents were blocked by replacement of K+ by Cs+ in the pipette solution, the remaining ICa was not affected by 10 microM CPA. 5. CPA (10 microM) did not affect the conductance of single maxi Ca(2+)-dependent K+ channels or the Cd(2+)-dependence of their open probability in both inside- and outside-out configurations. 6. These results indicate that IK-Ca is selectively and strongly suppressed by CPA.(ABSTRACT TRUNCATED AT 250 WORDS)

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Selected References

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  1. Amédée T., Large W. A., Wang Q. Characteristics of chloride currents activated by noradrenaline in rabbit ear artery cells. J Physiol. 1990 Sep;428:501–516. doi: 10.1113/jphysiol.1990.sp018224. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Benham C. D., Bolton T. B., Lang R. J., Takewaki T. Calcium-activated potassium channels in single smooth muscle cells of rabbit jejunum and guinea-pig mesenteric artery. J Physiol. 1986 Feb;371:45–67. doi: 10.1113/jphysiol.1986.sp015961. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Benham C. D., Bolton T. B. Spontaneous transient outward currents in single visceral and vascular smooth muscle cells of the rabbit. J Physiol. 1986 Dec;381:385–406. doi: 10.1113/jphysiol.1986.sp016333. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bielefeld D. R., Hume J. R., Krier J. Action potentials and membrane currents of isolated single smooth muscle cells of cat and rabbit colon. Pflugers Arch. 1990 Mar;415(6):678–687. doi: 10.1007/BF02584005. [DOI] [PubMed] [Google Scholar]
  5. Bolton T. B., Lim S. P. Properties of calcium stores and transient outward currents in single smooth muscle cells of rabbit intestine. J Physiol. 1989 Feb;409:385–401. doi: 10.1113/jphysiol.1989.sp017504. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Bourreau J. P., Abela A. P., Kwan C. Y., Daniel E. E. Acetylcholine Ca2+ stores refilling directly involves a dihydropyridine-sensitive channel in dog trachea. Am J Physiol. 1991 Sep;261(3 Pt 1):C497–C505. doi: 10.1152/ajpcell.1991.261.3.C497. [DOI] [PubMed] [Google Scholar]
  7. Carl A., McHale N. G., Publicover N. G., Sanders K. M. Participation of Ca2(+)-activated K+ channels in electrical activity of canine gastric smooth muscle. J Physiol. 1990 Oct;429:205–221. doi: 10.1113/jphysiol.1990.sp018252. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Cole W. C., Carl A., Sanders K. M. Muscarinic suppression of Ca2+-dependent K current in colonic smooth muscle. Am J Physiol. 1989 Sep;257(3 Pt 1):C481–C487. doi: 10.1152/ajpcell.1989.257.3.C481. [DOI] [PubMed] [Google Scholar]
  9. Cole W. C., Sanders K. M. Characterization of macroscopic outward currents of canine colonic myocytes. Am J Physiol. 1989 Sep;257(3 Pt 1):C461–C469. doi: 10.1152/ajpcell.1989.257.3.C461. [DOI] [PubMed] [Google Scholar]
  10. Deng H. W., Kwan C. Y. Cyclopiazonic acid is a sarcoplasmic reticulum Ca(2+)-pump inhibitor of rat aortic muscle. Zhongguo Yao Li Xue Bao. 1991 Jan;12(1):53–58. [PubMed] [Google Scholar]
  11. Désilets M., Driska S. P., Baumgarten C. M. Current fluctuations and oscillations in smooth muscle cells from hog carotid artery. Role of the sarcoplasmic reticulum. Circ Res. 1989 Sep;65(3):708–722. doi: 10.1161/01.res.65.3.708. [DOI] [PubMed] [Google Scholar]
  12. Ganitkevich V., Isenberg G. Isolated guinea pig coronary smooth muscle cells. Acetylcholine induces hyperpolarization due to sarcoplasmic reticulum calcium release activating potassium channels. Circ Res. 1990 Aug;67(2):525–528. doi: 10.1161/01.res.67.2.525. [DOI] [PubMed] [Google Scholar]
  13. Goeger D. E., Riley R. T., Dorner J. W., Cole R. J. Cyclopiazonic acid inhibition of the Ca2+-transport ATPase in rat skeletal muscle sarcoplasmic reticulum vesicles. Biochem Pharmacol. 1988 Mar 1;37(5):978–981. doi: 10.1016/0006-2952(88)90195-5. [DOI] [PubMed] [Google Scholar]
  14. Goeger D. E., Riley R. T. Interaction of cyclopiazonic acid with rat skeletal muscle sarcoplasmic reticulum vesicles. Effect on Ca2+ binding and Ca2+ permeability. Biochem Pharmacol. 1989 Nov 15;38(22):3995–4003. doi: 10.1016/0006-2952(89)90679-5. [DOI] [PubMed] [Google Scholar]
  15. Green K. A., Foster R. W., Small R. C. A patch-clamp study of K(+)-channel activity in bovine isolated tracheal smooth muscle cells. Br J Pharmacol. 1991 Apr;102(4):871–878. doi: 10.1111/j.1476-5381.1991.tb12269.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Hamill O. P., Marty A., Neher E., Sakmann B., Sigworth F. J. Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches. Pflugers Arch. 1981 Aug;391(2):85–100. doi: 10.1007/BF00656997. [DOI] [PubMed] [Google Scholar]
  17. Iino M. Calcium-induced calcium release mechanism in guinea pig taenia caeci. J Gen Physiol. 1989 Aug;94(2):363–383. doi: 10.1085/jgp.94.2.363. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Imaizumi Y., Muraki K., Watanabe M. Characteristics of transient outward currents in single smooth muscle cells from the ureter of the guinea-pig. J Physiol. 1990 Aug;427:301–324. doi: 10.1113/jphysiol.1990.sp018173. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Imaizumi Y., Muraki K., Watanabe M. Ionic currents in single smooth muscle cells from the ureter of the guinea-pig. J Physiol. 1989 Apr;411:131–159. doi: 10.1113/jphysiol.1989.sp017565. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Inoue R., Kitamura K., Kuriyama H. Two Ca-dependent K-channels classified by the application of tetraethylammonium distribute to smooth muscle membranes of the rabbit portal vein. Pflugers Arch. 1985 Oct;405(3):173–179. doi: 10.1007/BF00582557. [DOI] [PubMed] [Google Scholar]
  21. Kitamura K., Sakai T., Kajioka S., Kuriyama H. Activations of the Ca dependent K channel by Ca released from the sarcoplasmic reticulum of mammalian smooth muscles. Biomed Biochim Acta. 1989;48(5-6):S364–S369. [PubMed] [Google Scholar]
  22. Klöckner U., Isenberg G. Action potentials and net membrane currents of isolated smooth muscle cells (urinary bladder of the guinea-pig). Pflugers Arch. 1985 Dec;405(4):329–339. doi: 10.1007/BF00595685. [DOI] [PubMed] [Google Scholar]
  23. Komori S., Bolton T. B. Calcium release induced by inositol 1,4,5-trisphosphate in single rabbit intestinal smooth muscle cells. J Physiol. 1991 Feb;433:495–517. doi: 10.1113/jphysiol.1991.sp018440. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Komori S., Bolton T. B. Role of G-proteins in muscarinic receptor inward and outward currents in rabbit jejunal smooth muscle. J Physiol. 1990 Aug;427:395–419. doi: 10.1113/jphysiol.1990.sp018178. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Kurebayashi N., Ogawa Y. Discrimination of Ca(2+)-ATPase activity of the sarcoplasmic reticulum from actomyosin-type ATPase activity of myofibrils in skinned mammalian skeletal muscle fibres: distinct effects of cyclopiazonic acid on the two ATPase activities. J Muscle Res Cell Motil. 1991 Aug;12(4):355–365. doi: 10.1007/BF01738590. [DOI] [PubMed] [Google Scholar]
  26. Latorre R., Oberhauser A., Labarca P., Alvarez O. Varieties of calcium-activated potassium channels. Annu Rev Physiol. 1989;51:385–399. doi: 10.1146/annurev.ph.51.030189.002125. [DOI] [PubMed] [Google Scholar]
  27. Loirand G., Pacaud P., Baron A., Mironneau C., Mironneau J. Large conductance calcium-activated non-selective cation channel in smooth muscle cells isolated from rat portal vein. J Physiol. 1991 Jun;437:461–475. doi: 10.1113/jphysiol.1991.sp018606. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Ohya Y., Kitamura K., Kuriyama H. Cellular calcium regulates outward currents in rabbit intestinal smooth muscle cell. Am J Physiol. 1987 Apr;252(4 Pt 1):C401–C410. doi: 10.1152/ajpcell.1987.252.4.C401. [DOI] [PubMed] [Google Scholar]
  29. Ohya Y., Terada K., Kitamura K., Kuriyama H. Membrane currents recorded from a fragment of rabbit intestinal smooth muscle cell. Am J Physiol. 1986 Sep;251(3 Pt 1):C335–C346. doi: 10.1152/ajpcell.1986.251.3.C335. [DOI] [PubMed] [Google Scholar]
  30. Pacaud P., Loirand G., Lavie J. L., Mironneau C., Mironneau J. Calcium-activated chloride current in rat vascular smooth muscle cells in short-term primary culture. Pflugers Arch. 1989 Apr;413(6):629–636. doi: 10.1007/BF00581813. [DOI] [PubMed] [Google Scholar]
  31. Sakai T., Terada K., Kitamura K., Kuriyama H. Ryanodine inhibits the Ca-dependent K current after depletion of Ca stored in smooth muscle cells of the rabbit ileal longitudinal muscle. Br J Pharmacol. 1988 Dec;95(4):1089–1100. doi: 10.1111/j.1476-5381.1988.tb11743.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Seidler N. W., Jona I., Vegh M., Martonosi A. Cyclopiazonic acid is a specific inhibitor of the Ca2+-ATPase of sarcoplasmic reticulum. J Biol Chem. 1989 Oct 25;264(30):17816–17823. [PubMed] [Google Scholar]
  33. Sims S. M., Vivaudou M. B., Hillemeier C., Biancani P., Walsh J. V., Jr, Singer J. J. Membrane currents and cholinergic regulation of K+ current in esophageal smooth muscle cells. Am J Physiol. 1990 May;258(5 Pt 1):G794–G802. doi: 10.1152/ajpgi.1990.258.5.G794. [DOI] [PubMed] [Google Scholar]
  34. Takeda M., Imaizumi Y., Watanabe M. Effects of noradrenaline and heparin on outward current in single smooth muscle cells of the guinea-pig vas deferens. Eur J Pharmacol. 1991 Feb 14;193(3):375–378. doi: 10.1016/0014-2999(91)90155-j. [DOI] [PubMed] [Google Scholar]
  35. Terada K., Kitamura K., Kuriyama H. Different inhibitions of the voltage-dependent K+ current by Ca2+ antagonists in the smooth muscle cell membrane of rabbit small intestine. Pflugers Arch. 1987 May;408(6):558–564. doi: 10.1007/BF00581156. [DOI] [PubMed] [Google Scholar]
  36. Uyama Y., Imaizumi Y., Watanabe M. Effects of cyclopiazonic acid, a novel Ca(2+)-ATPase inhibitor, on contractile responses in skinned ileal smooth muscle. Br J Pharmacol. 1992 May;106(1):208–214. doi: 10.1111/j.1476-5381.1992.tb14316.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Vogalis F., Publicover N. G., Hume J. R., Sanders K. M. Relationship between calcium current and cytosolic calcium in canine gastric smooth muscle cells. Am J Physiol. 1991 May;260(5 Pt 1):C1012–C1018. doi: 10.1152/ajpcell.1991.260.5.C1012. [DOI] [PubMed] [Google Scholar]
  38. Wang Q., Large W. A. Noradrenaline-evoked cation conductance recorded with the nystatin whole-cell method in rabbit portal vein cells. J Physiol. 1991 Apr;435:21–39. doi: 10.1113/jphysiol.1991.sp018496. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Watanabe M., Imaizumi Y., Muraki K., Takeda M. A comparative study about voltage-dependent Ca currents in smooth muscle cells isolated from several tissues. Adv Exp Med Biol. 1989;255:119–128. doi: 10.1007/978-1-4684-5679-0_13. [DOI] [PubMed] [Google Scholar]

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