Evidence map›Paper›PMID 9679166›Full record

ArticleThe Journal of physiology1998

ATP-evoked increases in [Ca2+]i and peptide release from rat isolated neurohypophysial terminals via a P2X2 purinoceptor.

J D Troadec, S Thirion, G Nicaise, J R Lemos, G Dayanithi

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of physiology, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

34 citing papers in PubMed, 87 citations in OpenAlex.

  1. Review
  2. AVPVThe Journal of reproduction and development · 2024
    Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Purinergic signaling pathways in endocrine system.Autonomic neuroscience : basic & clinical · 2015
    Review
  8. Article
  9. Article
  10. Purinergic signalling in endocrine organs.Purinergic signalling · 2014
    Review
  11. Potentiation of inhibitory synaptic transmission by extracellular ATP in rat suprachiasmatic nuclei.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    Article
  12. P2X receptor channels in endocrine glands.Wiley interdisciplinary reviews. Membrane transport and signaling · 2013
    Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. Purinergic regulation of hypothalamopituitary functions.Trends in endocrinology and metabolism: TEM · 2009
    Review
  19. Article
  20. Article
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

5 authors at 3 institutions in 1 country.

J D TroadecUMR 6548-CNRS, Laboratoire de Physiologie Cellulaire et Moleculaire, Universite de Nice-Sophia Antipolis, F-06108 Nice, France. troadec@hermes.unice.fr
S Thirion
G Nicaise
J R Lemos
G Dayanithi
Laboratoire de physiologie cellulaire et moléculaireCentre National de la Recherche Scientifique · FRUniversité Côte d'Azur · FR

Funding

DEPOLARIZATION/SECRETION COUPLING IN NERVE TERMINALSR01NS029470 · NINDS · WORCESTER FOUNDATION FOR BIOMEDICAL RES · PI LEMOS, JOSE R · 1991 to 2012
$4.3M
NINDS NIH HHS NS29470NINDS NIH HHS R01 NS029470
6 · The paper itself

Abstract

1. The effect of externally applied ATP on cytosolic free Ca2+ concentration ([Ca2+]i) was tested in single isolated rat neurohypophysial nerve terminals by fura-2 imaging. The release of vasopressin (AVP) and oxytocin (OT) upon ATP stimulation was also studied from a population of terminals using specific radioimmunoassays. 2. ATP evoked a sustained [Ca2+]i increase, which was dose dependent in the 1-100 microM range (EC50 = 4.8 microM). This effect was observed in only approximately 40 % of the terminals. 3. Interestingly, ATP, in the same range (EC50 = 8.6 microM), evoked AVP, but no significant OT, release from these terminals. 4. Both the [Ca2+]i increase and AVP release induced by ATP were highly and reversibly inhibited by suramin, suggesting the involvement of a P2 purinergic receptor in the ATP-induced responses. Pyridoxal-5-phosphate-6-azophenyl-2',4'-disulphonic acid (PPADS), another P2 purinergic receptor antagonist, strongly reduced the ATP-induced [Ca2+]i response. 5. To further characterize the receptor, different agonists were tested, with the following efficacy: ATP = 2-methylthio-ATP > ATP-gamma-S > alpha, beta-methylene-ATP > ADP. The compounds adenosine, AMP, beta, gamma-methylene-ATP and UTP were ineffective. 6. The ATP-dependent [Ca2+]i increase was dependent on extracellular Ca2+ concentration ([Ca2+]o). Fluorescence-quenching experiments with Mn2+ showed that externally applied ATP triggered a Mn2+ influx. The ATP-induced [Ca2+]i increase and AVP release were independent of and additive to a K+-induced response, in addition to being insensitive to Cd2+. The ATP-induced [Ca2+]i increase was strongly reduced in the presence of Gd3+. These results suggest that the observed [Ca2+]i increases were elicited by Ca2+ entry through a P2X channel receptor rather than via a voltage-dependent Ca2+ channel. 7. We propose that ATP, co-released with neuropeptides, could act as a paracrine-autocrine messenger, stimulating, via Ca2+ entry through a P2X2 receptor, the secretion of AVP, in particular, from neurohypophysial nerve terminals.

Indexed as

Adenosine TriphosphateAnimalsArginine VasopressinCalciumCytosolKineticsMaleModels, BiologicalNerve EndingsOxytocinPituitary Gland, PosteriorRatsRats, WistarReceptors, Purinergic P2Receptors, Purinergic P2X2SuraminAdenosine TriphosphateArginine VasopressinCalciumOxytocinP2rx2 protein, ratReceptors, Purinergic P2Receptors, Purinergic P2X2Suramin

Identifiers

PMID9679166
PMCPMC2231092
OpenAlexW2026697636

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.