Evidence map›Paper›PMID 19199006›Full record

ArticleMolecular and cellular biochemistry2009

The identification of a caffeine-induced Ca2+ influx pathway in rat primary sensory neurons.

João Paulo L Daher, Tony D Gover, Thais H V Moreira, Vânia G S Lopes, Daniel Weinreich

Abstract read
In one paragraph

Article in Molecular and cellular biochemistry, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact, top 93% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. TRPA1, TRPV1, and Caffeine: Pain and Analgesia.International journal of molecular sciences · 2024
    Review
  3. Article
  4. The Taste of Caffeine.Journal of caffeine research · 2017
    Review
  5. 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 2 institutions in 2 countries.

João Paulo L DaherDepartment of Pathology, School of Medicine, Fluminense Federal University, 303 Marquês do Paraná Street, Room 4, Niterói, RJ 24033-900, Brazil. jpldaher@hotmail.com
Tony D Gover
Thais H V Moreira
Vânia G S Lopes
Daniel Weinreich
University of Maryland, Baltimore · USUniversidade Federal Fluminense · BR

Funding

CHEMORECEPTION AND SIGNAL PROCESSING IN VAGAL AFFERENTSR01NS022069 · NINDS · UNIVERSITY OF MARYLAND BALTIMORE · PI WEINREICH, DANIEL · 1985 to 2006
$1.7M
NINDS NIH HHS NS-22069NINDS NIH HHS R01 NS022069
6 · The paper itself

Abstract

Caffeine-induced Ca2+ transients (CICTs) in rabbit nodose ganglion neurons (NGNs) are produced by two distinct mechanisms: release from intracellular stores via ryanodine receptors and Ca2+ influx across the plasma membrane, due to activation of an unknown receptor. In isolated rat NGNs, we used single-cell microfluorimetry to measure changes in intracellular Ca2+ and to test whether TRPV1 receptors underlie the Ca2+ influx pathway. Caffeine (10 mM) evoked CICTs in all NGNs tested (n = 47) averaging 365 +/- 32 nM. CICTs were partially dependent upon a Ca2+ influx pathway that ranged between 33% and 98% of the total Ca2+ transient. Application of two selective TRPV1 antagonists significantly attenuated CICTs. The peak average amplitudes of CICTs in Ca2+-free Locke solution and Ca2+-free Locke solution with IRTX or with BCTC were not significantly different from one another (n = 5 and 7, respectively). These observations suggest that caffeine can induce Ca2+ influx by activating TRPV1 channels.

Indexed as

AnimalsCaffeineCalcium SignalingCentral Nervous System StimulantsMaleRatsRats, Sprague-DawleySensory Receptor CellsTRPV Cation ChannelsCaffeineCentral Nervous System StimulantsTRPV1 receptorTRPV Cation Channels

Identifiers

PMID19199006
PMCPMC3370888
OpenAlexW1983399115

What OpenQuestion holds

Textmetadata
LicenceTDM
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.