Literature DB >> 2754475

Phosphatidylinositol system's role in serotonin-induced facilitation at the crayfish neuromuscular junction.

D Dixon1, H L Atwood.   

Abstract

1. In a crustacean neuromuscular preparation, the walking leg opener muscle of the freshwater crayfish Procambarus clarkii, application of serotonin (1 microM) produces presynaptic depolarization and long-lasting facilitation of excitatory postsynaptic potentials (EPSPs). The frequency of spontaneously released transmitter quanta also increases. Facilitation of evoked EPSPs declines after serotonin application in two phases. 2. Serotonin-induced facilitation was examined using simultaneous pre- and postsynaptic intracellular microelectrode recording. A presynaptic microelectrode recorded action potentials and membrane potential of a presynaptic axonal branch, and one or more postsynaptic microelectrodes recorded EPSPs in muscle fibers innervated by the excitatory motor axon. Components of the phosphatidylinositol second messenger system and pharmacologic agents affecting this system were injected through the presynaptic electrode, and changes in synaptic transmission were measured. 3. Presynaptic injection of inositol 1,4,5-triphosphate (IP3) causes presynaptic depolarization, increases the frequency of spontaneously released transmitter quanta, and promotes a relatively short-lasting facilitation of evoked EPSPs. These actions are consistent with elevation of intracellular Ca2+ and resemble the early phase of serotonin-induced facilitation. 4. Application of a phorbol ester, 12-O-tetradecanoyl-phorbol-13-acetate (TPA), that activates protein kinase C (C-kinase), produces a long-lasting, low-level facilitation of evoked EPSPs. Application of another phorbol ester, phorbol-12-monoacetate (PTMA), which does not activate C-kinase has no effect. 5. Presynaptic injection of RA 233, a phospholipase C (PLP-C) inhibitor, blocks all aspects of serotonin-induced facilitation. This compound was found to have no general deleterious effects on synaptic transmission and does not block other forms of synaptic facilitation in this preparation.(ABSTRACT TRUNCATED AT 250 WORDS)

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2754475     DOI: 10.1152/jn.1989.62.1.239

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  7 in total

1.  Structure/function assessment of synapses at motor nerve terminals.

Authors:  A F M Johnstone; K Viele; R L Cooper
Journal:  Synapse       Date:  2010-09-17       Impact factor: 2.562

2.  Neuronal adaptations to changes in the social dominance status of crayfish.

Authors:  S R Yeh; B E Musolf; D H Edwards
Journal:  J Neurosci       Date:  1997-01-15       Impact factor: 6.167

3.  Calcium entry related to active zones and differences in transmitter release at phasic and tonic synapses.

Authors:  M Msghina; A G Millar; M P Charlton; C K Govind; H L Atwood
Journal:  J Neurosci       Date:  1999-10-01       Impact factor: 6.167

4.  Serotonin and the small cardioactive peptides differentially modulate two motor neurons that innervate the same muscle fibers in Aplysia.

Authors:  L E Fox; P E Lloyd
Journal:  J Neurosci       Date:  1997-08-15       Impact factor: 6.167

5.  Neuromodulators enhance transmitter release by two separate mechanisms at the inhibitor of crayfish opener muscle.

Authors:  A Vyshedskiy; K R Delaney; J W Lin
Journal:  J Neurosci       Date:  1998-07-15       Impact factor: 6.167

6.  Long-lasting synaptic facilitation induced by serotonin in superficial dorsal horn neurones of the rat spinal cord.

Authors:  Y Hori; K Endo; T Takahashi
Journal:  J Physiol       Date:  1996-05-01       Impact factor: 5.182

7.  Enhancement of synaptic responses in ascending interneurones following acquisition of social dominance in crayfish.

Authors:  Toshiki Abe; Toshiki Nagayama
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2021-03-27       Impact factor: 1.836

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.