Evidence map›Paper›PMID 9651199›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience1998

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

A Vyshedskiy, K R Delaney, J W Lin

Open access · greenAbstract readComparative Study
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 24% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 26 citations in OpenAlex.

  1. Enhancement of synaptic responses in ascending interneurones following acquisition of social dominance in crayfish.Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology · 2021
    Article
  2. Article
  3. Article
  4. Article
  5. Preferential potentiation of fast-releasing synaptic vesicles by cAMP at the calyx of Held.Proceedings of the National Academy of Sciences of the United States of America · 2001
    Article
  6. Article
  7. Article
  8. Modulation of transmission during trains at a cerebellar synapse.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2000
    Article
  9. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 2 countries.

A VyshedskiyDepartment of Biology, Boston University, Boston, Massachusetts 02215, USA.
K R Delaney
J W Lin
Boston University · USSimon Fraser University · CA

Funding

PLASTICITY AT A CRAYFISH NEUROMUSCULAR SYNAPSER01NS031707 · NINDS · BOSTON UNIVERSITY · PI LIN, JEN-WEI · 1999 to 2003
$849k
RELEASE MECHANISM AND PLASTICITY AT A TONIC SYNAPSER29NS031707 · NINDS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI LIN, JEN-WEI · 1994 to 1998
–
NINDS NIH HHS NS31707NINDS NIH HHS R01 NS031707
6 · The paper itself

Abstract

A presynaptic voltage control method has been used to investigate the modulatory effects of serotonin (5-HT) and okadaic acid (OA) on the inhibitory junction of the crayfish opener muscle. Instead of using action potentials, we used 20 msec pulses depolarized to 0 mV to activate transmitter release. This approach allowed us to monitor two separate physiological parameters related to the release process. The first parameter, transmitter release kinetics, is characterized as the delay when inhibitory postsynaptic conductance reaches its half-maximum (IPSG50). The second parameter, the total area of IPSG (IPSGarea), estimates total transmitter output. We have reported previously that the F2 component of synaptic facilitation is associated with a decrease in IPSG50 but without a change in IPSGarea. These results raised the possibility that IPSG50 and IPSGarea could be mediated by separate mechanisms that were modulated independently. To explore this possibility, we investigated the effects of 5-HT (100-200 nM) and OA (2.5 microM) on the two parameters. 5-HT and OA enhanced IPSG neither by changing the sensitivity of postsynaptic receptors, as tested by iontophoretically ejected GABA, nor by elevating resting and action potential-activated presynaptic free calcium, as monitored by fura-2 imaging. 5-HT and OA decreased IPSG50 by 3.0 +/- 1.4 and 3.6 +/- 1.1 msec, respectively, and increased IPSGarea by 50 +/- 21 and 37 +/- 6%, respectively. The ability of F2 facilitation to accelerate release kinetics was reduced in the presence of the modulators, suggesting that the mechanism underlying the accelerated release kinetics was shared by the two modes of synaptic enhancement. This report demonstrates that the acceleration in release kinetics and the increase in total release are two separate mechanisms for enhancing transmitter output and that these two mechanisms can be activated without changes in presynaptic calcium dynamics.

Indexed as

AnimalsAstacoideaCalciumMembrane PotentialsMusclesNeural InhibitionNeurotransmitter AgentsOkadaic AcidSerotoninSynaptic TransmissionCalciumNeurotransmitter AgentsOkadaic AcidSerotonin

Identifiers

PMID9651199
PMCPMC6793504
OpenAlexW2122882460

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.