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PMID: 2471780 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Calcium channels that are required for secretion from intact nerve terminals of vertebrates are sensitive to omega-conotoxin and relatively insensitive to dihydropyridines. Optical studies with and without voltage-sensitive dyes.

The Journal of general physiology ·Vol. 93 ·No. 4 ·1989-04-00 ·Pages 715-29

Obaid AL, Flores R, Salzberg BM

Abstract

Extrinsic absorption changes exhibited by potentiometric dyes have established the ionic basis of the action potential in synchronously activated populations of nerve terminals in the intact neurohypophyses of amphibia and mammals (Salzberg et al., 1983; Obaid et al., 1983, 1985b). Also, large and rapid changes in light scattering, measured as transparency, have been shown to follow membrane depolarization and to be intimately associated with the release of neuropeptides from the nerve terminals of the mouse neurohypophysis (Salzberg et al., 1985; Gainer et al., 1986). We report some experiments that help to define the pharmacological profile of the calcium channels present in intact neurosecretory terminals of vertebrates. For these, we used the peptide toxin omega-conotoxin GVIA (1-5 microM) and the dihydropyridine compounds Bay-K 8644 and nifedipine (2-5 microM), together with the after-hyperpolarization of the nerve terminal action potential. This undershoot depends upon the activation of a calcium-mediated potassium channel, as suggested by its sensitivity to [Ca++]o and charybdotoxin. omega-conotoxin GVIA substantially reduced the after-hyperpolarization in neurosecretory terminals of Xenopus, while neither of the dihydropyridine compounds had any effect under conditions that mimic natural stimulation. The effects of these calcium channel modifiers on the action potential recorded optically from the terminals of the Xenopus neurohypophysis were faithfully reflected in the behavior of the light-scattering changes observed in the neurohypophysis of the CD-1 mouse. omega-conotoxin GVIA (5 microM) reduced the size of the intrinsic optical signal associated with secretion by 50%, while the dihydropyridines had little effect. These observations suggest that the type of calcium channel that dominates the secretory behavior of intact vertebrate nerve terminals is at least partially blocked by omega-conotoxin GVIA and is insensitive, under normal conditions, to dihydropyridines.

MeSH Terms
3-Pyridinecarboxylic acid, 1,4-dihydro-2,6-dimethyl-5-nitro-4-(2-(trifluoromethyl)phenyl)-, Methyl ester/pharmacology Action Potentials Animals Axons/cytology Calcium Channels/metabolism Conotoxins Mollusk Venoms/pharmacology Nerve Fibers Nifedipine/pharmacology Pituitary Gland, Posterior Time Factors Xenopus laevis
Chemicals
Calcium Channels Conotoxins Mollusk Venoms 3-Pyridinecarboxylic acid, 1,4-dihydro-2,6-dimethyl-5-nitro-4-(2-(trifluoromethyl)phenyl)-, Methyl ester conotoxin GV Nifedipine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Obaid A L
David Mahoney Institute of Neurological Science, Department of Physiology, School of Medicine, University of Pennsylvania, Philadelphia 19104-6085.
Flores R
Salzberg B M
References (40)
40 references, click to expand
  1. Real-time optical mapping of neuronal activity: from single growth cones to the intact mammalian brain.
    Annu Rev Neurosci. 1985;8:263-305 PMID: 3885828
  2. Charybdotoxin, a protein inhibitor of single Ca2+-activated K+ channels from mammalian skeletal muscle.
    Nature. 1985 Jan 24-30;313(6000):316-8 PMID: 2578618
  3. Three types of neuronal calcium channel with different calcium agonist sensitivity.
    Nature. 1985 Aug 1-7;316(6027):440-3 PMID: 2410796
  4. Large and rapid changes in light scattering accompany secretion by nerve terminals in the mammalian neurohypophysis.
    J Gen Physiol. 1985 Sep;86(3):395-411 PMID: 2997364
  5. Peptide neurotoxins from fish-hunting cone snails.
    Science. 1985 Dec 20;230(4732):1338-43 PMID: 4071055
  6. Early events in development of electrical activity and contraction in embryonic rat heart assessed by optical recording.
    J Physiol. 1985 Dec;369:209-27 PMID: 4093880
  7. Optical monitoring of membrane potential: methods of multisite optical measurement.
    Soc Gen Physiol Ser. 1986;40:71-99 PMID: 3520842
  8. Action potentials and frequency-dependent secretion in the mouse neurohypophysis.
    Neuroendocrinology. 1986;43(5):557-63 PMID: 3018612
  9. Brain voltage-sensitive calcium channel subtypes differentiated by omega-conotoxin fraction GVIA.
    Proc Natl Acad Sci U S A. 1986 Nov;83(22):8804-7 PMID: 2430302
  10. Multiple calcium channels and neuronal function.
    Science. 1987 Jan 2;235(4784):46-52 PMID: 2432656
  11. Involvement of dihydropyridine receptors in excitation-contraction coupling in skeletal muscle.
    Nature. 1987 Feb 19-25;325(6106):717-20 PMID: 2434854
  12. Omega-conotoxin: direct and persistent blockade of specific types of calcium channels in neurons but not muscle.
    Proc Natl Acad Sci U S A. 1987 Jun;84(12):4327-31 PMID: 2438698
  13. Calcium channels: mechanisms of selectivity, permeation, and block.
    Annu Rev Biophys Biophys Chem. 1987;16:265-90 PMID: 2439098
  14. Identification of the receptor for omega-conotoxin in brain. Probable components of the calcium channel.
    J Biol Chem. 1987 Jul 15;262(20):9877-82 PMID: 2439513
  15. Transmitter release from presynaptic terminals of electric organ: inhibition by the calcium channel antagonist omega Conus toxin.
    J Neurosci. 1987 Aug;7(8):2390-6 PMID: 3112325
  16. Dihydropyridine inhibition of neuronal calcium current and substance P release.
    Pflugers Arch. 1987 Aug;409(4-5):361-6 PMID: 2442705
  17. Sodium currents in dissociated bull-frog sympathetic neurones.
    J Physiol. 1987 Aug;389:605-27 PMID: 2445980
  18. Dominant role of N-type Ca2+ channels in evoked release of norepinephrine from sympathetic neurons.
    Science. 1988 Jan 1;239(4835):57-61 PMID: 2447647
  19. Characterization of the electrically evoked release of substance P from dorsal root ganglion neurons: methods and dihydropyridine sensitivity.
    J Neurosci. 1988 Feb;8(2):463-71 PMID: 2448433
  20. Hormone release from isolated nerve endings of the rat neurohypophysis.
    J Physiol. 1987 Sep;390:55-70 PMID: 2450999
  21. Kinetic and pharmacological properties distinguishing three types of calcium currents in chick sensory neurones.
    J Physiol. 1987 Dec;394:149-72 PMID: 2451016
  22. Optical recording of electrical activity from parallel fibres and other cell types in skate cerebellar slices in vitro.
    J Physiol. 1987 Dec;393:681-702 PMID: 3446807
  23. Changes in light scattering that accompany the action potential in squid giant axons: potential-dependent components.
    J Physiol. 1972 Aug;224(3):701-25 PMID: 5071934
  24. Changes in axon light scattering that accompany the action potential: current-dependent components.
    J Physiol. 1972 Aug;224(3):727-52 PMID: 5071935
  25. Changes in absorption, fluorescence, dichroism, and Birefringence in stained giant axons: : optical measurement of membrane potential.
    J Membr Biol. 1977 May 6;33(1-2):141-83 PMID: 864685
  26. Optical recording of neuronal activity in an invertebrate central nervous system: simultaneous monitoring of several neurons.
    J Neurophysiol. 1977 Nov;40(6):1281-91 PMID: 925730
  27. Stimulus-secretion coupling: variations on the theme of calcium-activated exocytosis involving cellular and extracellular sources of calcium.
    Ciba Found Symp. 1978;(54):61-90 PMID: 248020
  28. The effects of some organic "calcium antagonists" on calcium influx in presynaptic nerve terminals.
    Mol Pharmacol. 1979 Sep;16(2):576-86 PMID: 316102
  29. Improvements in optical methods for measuring rapid changes in membrane potential.
    J Membr Biol. 1981 Feb 15;58(2):123-37 PMID: 7218335
  30. Localization of pacemaking activity in early embryonic heart monitored using voltage-sensitive dye.
    Nature. 1981 Apr 16;290(5807):595-7 PMID: 7219544
  31. Calcium channel.
    Annu Rev Neurosci. 1981;4:69-125 PMID: 6261668
  32. Simultaneous optical monitoring of activity of many neurons in invertebrate ganglia using a 124-element photodiode array.
    J Neurophysiol. 1981 May;45(5):829-40 PMID: 6264048
  33. Visualization of the spread of electrical activity in rat hippocampal slices by voltage-sensitive optical probes.
    J Physiol. 1982 Dec;333:269-91 PMID: 7182467
  34. Multiple-site optical recording of membrane potential from a salivary gland. Interaction of synaptic and electrotonic excitation.
    J Gen Physiol. 1983 Jun;81(6):887-908 PMID: 6875509
  35. Rapid photochemical inactivation of Ca2+-antagonists shows that Ca2+ entry directly activates contraction in frog heart.
    Nature. 1983 Aug 18-24;304(5927):635-8 PMID: 6308474
  36. Optical monitoring of activity from many areas of the in vitro and in vivo salamander olfactory bulb: a new method for studying functional organization in the vertebrate central nervous system.
    J Neurosci. 1983 Nov;3(11):2251-62 PMID: 6631479
  37. Optical recording of action potentials from vertebrate nerve terminals using potentiometric probes provides evidence for sodium and calcium components.
    Nature. 1983 Nov 3-9;306(5938):36-40 PMID: 6633657
  38. Optical measurements of potential changes in axons and processes of neurons of a barnacle ganglion.
    J Neurosci. 1984 Mar;4(3):659-72 PMID: 6707730
  39. Are dihydropyridine binding sites voltage sensitive calcium channels?
    Life Sci. 1984 Mar 26;34(13):1205-21 PMID: 6323901
  40. Active calcium responses recorded optically from nerve terminals of the frog neurohypophysis.
    J Gen Physiol. 1985 Apr;85(4):481-9 PMID: 2409215
Article Info
Journal
The Journal of general physiology
Abbr.
J Gen Physiol
ISSN
0022-1295
Published
1989-04-00
Pages
715-29
Language
English
Region
United States
NLM ID
2985110R
PMCID
PMC2216227
Subset
IM
Grants
NINDS NIH HHS · NS-16824 · United States
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