Literature DB >> 1323666

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

X Wang1, S N Treistman, J R Lemos.   

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.

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Year:  1992        PMID: 1323666      PMCID: PMC1179977          DOI: 10.1113/jphysiol.1992.sp018919

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


  45 in total

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2.  Pharmacological characterization of voltage-dependent calcium currents in rat hippocampal neurons.

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3.  Ca2+ channels in rat central and peripheral neurons: high-threshold current resistant to dihydropyridine blockers and omega-conotoxin.

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4.  Single channels and ionic currents in peptidergic nerve terminals.

Authors:  J R Lemos; J J Nordmann; I M Cooke; E L Stuenkel
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5.  Effects of membrane depolarization on intracellular calcium in single nerve terminals.

Authors:  E L Stuenkel
Journal:  Brain Res       Date:  1990-10-08       Impact factor: 3.252

6.  Multiple components of both transient and sustained barium currents in a rat dorsal root ganglion cell line.

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Journal:  J Physiol       Date:  1990-01       Impact factor: 5.182

7.  Subtypes of voltage-sensitive calcium channels in cultured rat brain neurons.

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8.  Diversity of Conus neuropeptides.

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9.  A fast, transient K+ current in neurohypophysial nerve terminals of the rat.

Authors:  P J Thorn; X M Wang; J R Lemos
Journal:  J Physiol       Date:  1991-01       Impact factor: 5.182

10.  Ionic channels and hormone release from peptidergic nerve terminals.

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  33 in total

1.  An R-type Ca(2+) current in neurohypophysial terminals preferentially regulates oxytocin secretion.

Authors:  G Wang; G Dayanithi; R Newcomb; J R Lemos
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2.  Voltage-dependent membrane capacitance in rat pituitary nerve terminals due to gating currents.

Authors:  G Kilic; M Lindau
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3.  Adenosine inhibition via A(1) receptor of N-type Ca(2+) current and peptide release from isolated neurohypophysial terminals of the rat.

Authors:  Gang Wang; Govindan Dayanithi; Edward E Custer; José R Lemos
Journal:  J Physiol       Date:  2002-05-01       Impact factor: 5.182

4.  Contribution of L-type Ca(2+) channels to evoked transmitter release in cultured Xenopus nerve-muscle synapses.

Authors:  O Sand; B M Chen; A D Grinnell
Journal:  J Physiol       Date:  2001-10-01       Impact factor: 5.182

5.  Ca2+- and voltage-dependent inactivation of Ca2+ channels in nerve terminals of the neurohypophysis.

Authors:  J L Branchaw; M I Banks; M B Jackson
Journal:  J Neurosci       Date:  1997-08-01       Impact factor: 6.167

6.  mu-opioid receptor activation inhibits N- and P-type Ca2+ channel currents in magnocellular neurones of the rat supraoptic nucleus.

Authors:  B L Soldo; H C Moises
Journal:  J Physiol       Date:  1998-12-15       Impact factor: 5.182

7.  Identification of a vesicular pool of calcium channels in the bag cell neurons of Aplysia californica.

Authors:  B H White; L K Kaczmarek
Journal:  J Neurosci       Date:  1997-03-01       Impact factor: 6.167

8.  Developmental changes in calcium current pharmacology and somatostatin inhibition in chick parasympathetic neurons.

Authors:  M G White; M A Crumling; S D Meriney
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9.  Voltage-gated calcium currents in the magnocellular neurosecretory cells of the rat supraoptic nucleus.

Authors:  T E Fisher; C W Bourque
Journal:  J Physiol       Date:  1995-08-01       Impact factor: 5.182

10.  Distinct omega-agatoxin-sensitive calcium currents in somata and axon terminals of rat supraoptic neurones.

Authors:  T E Fisher; C W Bourque
Journal:  J Physiol       Date:  1995-12-01       Impact factor: 5.182

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