Evidence map›Paper›PMID 18818902›Full record

ArticleNaunyn-Schmiedeberg's archives of pharmacology2009

Tramadol-induced block of hyperpolarization-activated cation current in rat pituitary lactotrophs.

Yen-Chin Liu, Ya-Jean Wang, Pei-Yu Wu, Sheng-Nan Wu

Abstract read
PubMed Publisher
In one paragraph

Article in Naunyn-Schmiedeberg's archives of pharmacology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

22 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Cannabidiol Modulates M-Type KBiomedicines · 2023
    Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Effectiveness in the Block by Honokiol, a Dimerized Allylphenol fromInternational journal of molecular sciences · 2020
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Characterization of Effectiveness in ConcertedInternational journal of molecular sciences · 2020
    Article
  16. Article
  17. Evidence for Effective Multiple KFrontiers in pharmacology · 2019
    Article
  18. HCN Channels Modulators: The Need for Selectivity.Current topics in medicinal chemistry · 2016
    Review
  19. Review
  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

4 authors at 2 institutions in 1 country.

Yen-Chin LiuDepartment of Anesthesiology, National Cheng Kung University Medical College, Tainan, Taiwan.
Ya-Jean Wang
Pei-Yu Wu
Sheng-Nan Wu
National Cheng Kung University · TWKaohsiung Medical University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The hyperpolarization-activated cation current (I (h)) in rat pituitary lactotrophs (GH(3) cells) was characterized. Tramadol-induced block of this current was investigated. Effects of various related compounds on I (h) in GH(3) cells were also compared. Tramadol caused a time- and concentration-dependent reduction in the amplitude of I (h) with an IC(50) value of 13.6 microM. ZD7288 (30 microM), CsCl (2 mM), and propofol (30 microM) were effective in suppressing the amplitude of I (h). 2',5'-dideoxyadenosine (100 microM) suppressed I (h), while sp-cAMPS (100 microM) had no effect on it. Tramadol (10 microM) shifted the activation curve of I (h) to a more negative potential by approximately -20 mV, although no change in the slope factor was observed. Under current-clamp configuration, tramadol (10 microM) could reduce the firing frequency of action potentials. Intracellular Ca(2+) measurements revealed its ability to reduce spontaneous Ca(2+) oscillations in GH(3) cells. The results suggests that during cell exposure to tramadol used at clinically relevant concentration, the tramadol-mediated inhibition of I (h) could be direct and mediated via a non-opioid mechanism and would be one of the ionic mechanisms underlying reduced cell excitability.

Indexed as

Action PotentialsAnalgesics, OpioidAnimalsCationsCell LineCesiumChloridesCyclic AMPCyclic Nucleotide-Gated Cation ChannelsDideoxyadenosineHyperpolarization-Activated Cyclic Nucleotide-Gated ChannelsLactotrophsPatch-Clamp TechniquesPotassium ChannelsPropofolPyrimidines2',5'-dideoxyadenosineadenosine-3',5'-cyclic phosphorothioateAnalgesics, OpioidCationsCesiumcesium chlorideChloridesCyclic AMPCyclic Nucleotide-Gated Cation ChannelsDideoxyadenosineHyperpolarization-Activated Cyclic Nucleotide-Gated ChannelsICI D2788Potassium ChannelsPropofolPyrimidinesThionucleotidesTramadol

Identifiers

PMID18818902
OpenAlexW2059423367

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.