Noradrenaline modulates transmitter release by enhancing the Ca2+ sensitivity of exocytosis in the chick ciliary presynaptic terminal

Hiromu Yawo

    Research output: Contribution to journalArticle

    28 Citations (Scopus)

    Abstract

    1. The giant presynaptic terminal of chick ciliary ganglion was used to examine how noradrenaline (NA) modulates neurotransmitter release. The cholinergic excitatory postsynaptic currents (EPSCs) were recorded under whole-cell voltage clamp of the postsynaptic neuron. 2. Although the EPSC was potentiated by NA, the current directly activated by acetylcholine (IACh) was unaffected. NA also increased the quantal contents without changing the quantal size. 3. The NA-dependent potentiation was antagonized by neither phentolamine nor propranolol. The EPSC was also potentiated by adrenaline and dopamine but not by normetanephrine, phenylephrine or isoprenaline. The EPSC was attenuated by clonidine. Therefore, NA potentiated the transmitter release through a receptor pharmacologically different from both α- and β-adrenergic receptors. 4. The Ca2+ increment produced by an action potential (Δ[Ca2+]pre) was reduced by NA through an α2-adrenergic receptor. However, when α2-adrenergic receptors were blocked, neither α[Ca2+]pre nor resting Ca2+ were changed by NA. 5. The [Ca2+]0-EPSC relation was shifted by NA, decreasing the half-saturating [Ca2+J0, without changing the maximum. 6. It is concluded that NA-dependent potentiation of transmitter release was due to an increase in the Ca2+ sensitivity of the exocytotic process. The enhancement of the fusion probability is suggested.

    Original languageEnglish
    Pages (from-to)385-391
    Number of pages7
    JournalJournal of Physiology
    Volume493
    Issue number2
    DOIs
    Publication statusPublished - 1996 Jun 1

    ASJC Scopus subject areas

    • Physiology

    Fingerprint Dive into the research topics of 'Noradrenaline modulates transmitter release by enhancing the Ca<sup>2+</sup> sensitivity of exocytosis in the chick ciliary presynaptic terminal'. Together they form a unique fingerprint.

  • Cite this