Evidence map›Paper›PMID 8146014›Full record

ArticlePflugers Archiv : European journal of physiology1994

Effects of caffeine on intracellular calcium, calcium current and calcium-dependent potassium current in anterior pituitary GH3 cells.

R H Kramer, R Mokkapatti, E S Levitan

Abstract read
PubMed Publisher
In one paragraph

Article in Pflugers Archiv : European journal of physiology, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 39% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. TRPA1, TRPV1, and Caffeine: Pain and Analgesia.International journal of molecular sciences · 2024
    Review
  4. Review
  5. Article
  6. Bile acids induce CaBiochemistry and biophysics reports · 2022
    Article
  7. Review
  8. Article
  9. Caffeine-sensitive calcium stores regulate synaptic transmission from retinal rod photoreceptors.The Journal of neuroscience : the official journal of the Society for Neuroscience · 1999
    Article
  10. Article
  11. Article
  12. 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

3 authors at 1 institution in 1 country.

R H KramerCenter for Neurobiology and Behavior, Columbia University of Physicians and Surgeons, New York, NY 10032.
R Mokkapatti
E S Levitan
University of Pittsburgh · US

Funding

REGULATION OF PITUITARY ION CHANNELSR29NS029804 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LEVITAN, EDWIN S · 1991 to 1995
–
DETECTION OF CYCLIC NUCLEOTIDES IN INTACT NEURONSR29NS030685 · NINDS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI KRAMER, RICHARD H · 1992 to 1996
–
NINDS NIH HHS NS29804NINDS NIH HHS NS30685
6 · The paper itself

Abstract

Caffeine elicits physiological responses in a variety of cell types by triggering the mobilization of Ca2+ from intracellular organelles. Here we investigate the effects of caffeine on intracellular Ca2+ concentration ([Ca2+]i) and ionic currents in anterior pituitary cells (GH3) cells. Caffeine has a biphasic effect on Ca(2+)-activated K+ current [IK(Ca)]: it induces a transient increase superimposed upon a sustained inhibition. While the transient increase coincides with a rise in [Ca2+]i, the sustained inhibition of IK(Ca) is correlated with a sustained inhibition of the L-type Ca2+ current. The L-type Ca2+ current is also inhibited by other agents that mobilize intracellular Ca2+, including thyrotropin releasing hormone (TRH) and ryanodine, but in a matter distinct from caffeine. Unlike the caffeine effect, the TRH-induced inhibition "washes-out" under whole-cell patch-clamp conditions and is eliminated by intracellular Ca2+ chelators. Likewise, the ryanodine-induced inhibition desensitizes while the caffeine-induced inhibition does not. Simultaneous [Ca2+]i and Ca2+ current measurements show that caffeine can inhibit Ca2+ current without changing [Ca2+]i. Single-channel recordings show that caffeine reduces mean open time without affecting single-channel conductance of L-type channels. Hence the effects of caffeine on ion channels in GH3 cells are attributable both to mobilization of intracellular Ca2+ and to a direct effect on the gating of L-type Ca2+ channels.

Indexed as

AnimalsCaffeineCalciumCalcium ChannelsCell LineIntracellular FluidIon TransportPituitary Gland, AnteriorPotassiumRatsCaffeineCalciumCalcium ChannelsPotassium

Identifiers

PMID8146014
OpenAlexW2080529841

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.