Home LiteratureArticle Details
PMID: 1323666 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Two types of high-threshold calcium currents inhibited by omega-conotoxin in nerve terminals of rat neurohypophysis.

The Journal of physiology ·Vol. 445 ·1992-01-00 ·Pages 181-99

Wang X, Treistman SN, Lemos JR

Abstract

1. The neurohypophysis comprises the nerve terminals of hypothalamic neurosecretory cells, which contain arginine vasopressin (AVP) and oxytocin. The secretory terminals of rat neurohypophyses were acutely dissociated. The macroscopic calcium currents (ICa) of these isolated peptidergic terminals were studied using 'whole-cell' patch-clamp recording techniques. 2. There are two types ('Nt' (where the subscript 't' denotes terminal) and 'L') of high-threshold voltage-activated ICa in the terminals, which can be distinguished by holding at different potentials i.e. -90 and -50 mV. Replacement of Ca2+ in the bathing solution by Ba2+ increased the amplitude of ICa, primarily due to an increase in the L-type component. Both inward currents were eliminated by adding 50 microM-Cd2+ or when in a Ca(2+)-free bathing solution. 3. omega-Conotoxin GVIA (omega-CgTx) has been widely used as a Ca2+ channel blocker. However, whether this toxin can discriminate between different types of Ca2+ channels is still a subject of controversy. We applied omega-CgTx over a wide range of concentrations (0.01-2 microM) to examine its effects on both Nt- and L-type ICa in these terminals. At a concentration of 30 nM, omega-CgTx selectively reduced, by 48%, the amplitude of Nt-type ICa. In contrast, a higher concentration (300 nM) of omega-CgTx was necessary to inhibit the L-type ICa. 4. omega-CgTx inhibited both Nt- and L-type ICa in a dose-dependent manner, and the half-maximum inhibition (IC50) of the ICa by the toxin was 50 and 513 nM, respectively, which was approximately a tenfold difference. The reduction in both types of currents did not result from any shift in their current-voltage or steady-state inactivation relationships. 5. In contrast, omega-CgTx, at a concentration of 300 nM, had no effect on the tetrodotoxin-sensitive sodium current (INa) of the isolated peptidergic nerve terminals. Furthermore, omega-CgTx did not reduce the long-lasting, non-inactivating ICa in the isolated non-neuronal secretory cells of the pars intermedia (PI) (intermediate lobe of the pituitary). 6. Our studies suggest that omega-CgTx might exert specific blocking effects on both Nt- and L-type Ca2+ channels, but that in the isolated peptidergic nerve terminals, the Nt-type component is more susceptible to this toxin.

MeSH Terms
Action Potentials/drug effects Animals Calcium Channels/drug effects Dose-Response Relationship, Drug Electric Stimulation Immunoblotting/methods Male Mollusk Venoms/pharmacology Nerve Endings/drug effects Peptides/analysis Peptides, Cyclic/pharmacology Pituitary Gland, Posterior/chemistry,drug effects Rats Rats, Inbred Strains omega-Conotoxin GVIA
Chemicals
Calcium Channels Mollusk Venoms Peptides Peptides, Cyclic omega-Conotoxin GVIA
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Wang X
Neurobiology Group, Worcester Foundation for Experimental Biology, Shrewsbury, MA 01545.
Treistman S N
Lemos J R
References (45)
45 references, click to expand
  1. Pharmacological characterization of voltage-dependent calcium currents in rat hippocampal neurons.
    Neurosci Lett. 1990 Apr 20;112(1):70-5 PMID: 1696706
  2. Evidence for multiple types of Ca2+ channels in acutely isolated hippocampal CA3 neurones of the guinea-pig.
    J Physiol. 1991 Feb;433:259-81 PMID: 1668752
  3. Ca2+ channels in rat central and peripheral neurons: high-threshold current resistant to dihydropyridine blockers and omega-conotoxin.
    Neuron. 1991 Feb;6(2):269-80 PMID: 1847065
  4. A fast, transient K+ current in neurohypophysial nerve terminals of the rat.
    J Physiol. 1991 Jan;432:313-26 PMID: 1886058
  5. Multiple components of both transient and sustained barium currents in a rat dorsal root ganglion cell line.
    J Physiol. 1990 Jan;420:223-45 PMID: 2157839
  6. Diversity of Conus neuropeptides.
    Science. 1990 Jul 20;249(4966):257-63 PMID: 2165278
  7. Subtypes of voltage-sensitive calcium channels in cultured rat brain neurons.
    Neurosci Lett. 1990 Jul 31;115(2-3):300-6 PMID: 2172873
  8. Effects of membrane depolarization on intracellular calcium in single nerve terminals.
    Brain Res. 1990 Oct 8;529(1-2):96-101 PMID: 2282508
  9. Single channels and ionic currents in peptidergic nerve terminals.
    Nature. 1986 Jan 30-Feb 5;319(6052):410-2 PMID: 2418363
  10. Ionic channels and hormone release from peptidergic nerve terminals.
    J Exp Biol. 1986 Sep;124:53-72 PMID: 2428909
  11. 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
  12. Differential blocking action of synthetic omega-conotoxin on components of Ca2+ channel current in clonal GH3 cells.
    Neurosci Lett. 1987 Mar 31;75(2):235-9 PMID: 2437501
  13. Presynaptic Ca-antagonist omega-conotoxin irreversibly blocks N-type Ca-channels in chick sensory neurons.
    Neurosci Res. 1987 Feb;4(3):228-35 PMID: 2437502
  14. Omega-conotoxin does not block the verapamil-sensitive calcium channels at mouse motor nerve terminals.
    Neurosci Lett. 1987 Nov 23;82(2):177-80 PMID: 2447536
  15. 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
  16. Hormone release from isolated nerve endings of the rat neurohypophysis.
    J Physiol. 1987 Sep;390:55-70 PMID: 2450999
  17. Omega-conotoxin binding and effects on calcium channel function in human neuroblastoma and rat pheochromocytoma cell lines.
    FEBS Lett. 1988 Aug 1;235(1-2):178-82 PMID: 2456948
  18. 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.
    J Gen Physiol. 1989 Apr;93(4):715-29 PMID: 2471780
  19. Two types of calcium channels coexist in peptide-releasing vertebrate nerve terminals.
    Neuron. 1989 May;2(5):1419-26 PMID: 2560641
  20. Elementary properties and pharmacological sensitivities of calcium channels in mammalian peripheral neurons.
    Neuron. 1989 May;2(5):1453-63 PMID: 2560643
  21. Direct identification of individual vasopressin-containing nerve terminals of the rat neurohypophysis after 'whole-cell' patch-clamp recordings.
    Neurosci Lett. 1991 Mar 11;124(1):125-8 PMID: 1857538
  22. Ethanol reduces vasopressin release by inhibiting calcium currents in nerve terminals.
    Brain Res. 1991 Jun 14;551(1-2):338-41 PMID: 1913165
  23. Voltage-activated calcium currents in presynaptic nerve terminals of the chicken ciliary ganglion.
    J Physiol. 1990 Sep;428:199-213 PMID: 2172522
  24. Two components of high-threshold Ca2+ current inactivate by different mechanisms.
    Neuron. 1990 Oct;5(4):445-52 PMID: 2206532
  25. The calcium channel antagonist omega-conotoxin inhibits secretion from peptidergic nerve terminals.
    Biochem Biophys Res Commun. 1988 Oct 14;156(1):255-62 PMID: 3178834
  26. Depolarization-induced Ca2+ increase in isolated neurosecretory nerve terminals measured with fura-2.
    Proc Natl Acad Sci U S A. 1987 Mar;84(5):1439-43 PMID: 3469676
  27. Inactivation of Ca channels.
    Prog Biophys Mol Biol. 1984;44(3):215-67 PMID: 6095365
  28. Purification and sequence of a presynaptic peptide toxin from Conus geographus venom.
    Biochemistry. 1984 Oct 23;23(22):5087-90 PMID: 6509012
  29. Three types of neuronal calcium channel with different calcium agonist sensitivity.
    Nature. 1985 Aug 1-7;316(6027):440-3 PMID: 2410796
  30. Single ion channel activity in peptidergic nerve terminals of the isolated rat neurohypophysis related to stimulation of neural stalk axons.
    Brain Res. 1986 Sep 24;383(1-2):279-86 PMID: 2429729
  31. Characterization of the omega-conotoxin target. Evidence for tissue-specific heterogeneity in calcium channel types.
    Biochemistry. 1987 Feb 10;26(3):820-4 PMID: 2436655
  32. 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
  33. 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
  34. Properties of structure and interaction of the receptor for omega-conotoxin, a polypeptide active on Ca2+ channels.
    Biochem Biophys Res Commun. 1988 Feb 15;150(3):1051-62 PMID: 2449205
  35. Multiple types of neuronal calcium channels and their selective modulation.
    Trends Neurosci. 1988 Oct;11(10):431-8 PMID: 2469160
  36. Characterization of two kinds of high-voltage-activated Ca-channel currents in chick sensory neurons. Differential sensitivity to dihydropyridines and omega-conotoxin GVIA.
    Pflugers Arch. 1989 Jun;414(2):150-6 PMID: 2547195
  37. Omega-conotoxin blockade distinguishes Ca from Na permeable states in neuronal calcium channels.
    Pflugers Arch. 1988 Nov;413(1):14-22 PMID: 2851129
  38. Calcium channel antagonists. Omega-conotoxin defines a new high affinity site.
    J Biol Chem. 1986 May 15;261(14):6230-3 PMID: 2939072
  39. Isolated neurosecretory nerve endings as a tool for studying the mechanism of stimulus-secretion coupling.
    Biosci Rep. 1987 May;7(5):411-26 PMID: 3315032
  40. Increased sensitivity in peroxidase immunocytochemistry. A comparative study of a number of peroxidase visualization methods employing a model system.
    Histochemistry. 1986;84(3):221-30 PMID: 3519544
  41. Synthetic omega-conotoxin: a potent calcium channel blocking neurotoxin.
    Brain Res. 1987 Oct 20;424(1):58-64 PMID: 3690303
  42. Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches.
    Pflugers Arch. 1981 Aug;391(2):85-100 PMID: 6270629
  43. A venom peptide with a novel presynaptic blocking action.
    Nature. 1984 Mar 15-21;308(5956):282-4 PMID: 6608056
  44. A dot-immunobinding assay for monoclonal and other antibodies.
    Anal Biochem. 1982 Jan 1;119(1):142-7 PMID: 7072935
  45. Failure of omega-conotoxin to block L-channels associated with [3H]5-HT release in rat brain slices.
    Neurosci Lett. 1990 Jul 31;115(2-3):323-8 PMID: 1700344
Article Info
Journal
The Journal of physiology
Abbr.
J Physiol
ISSN
0022-3751
Published
1992-01-00
Pages
181-99
Language
English
Region
England
NLM ID
0266262
PMCID
PMC1179977
Subset
IM
Grants
NIAAA NIH HHS · AA08003 · United States
NIADDK NIH HHS · AM 16166 · United States
NINDS NIH HHS · NS29470 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com