Evidence map›Paper›PMID 26725735›Full record

ReviewActa pharmacologica Sinica2016

Peptide toxins and small-molecule blockers of BK channels.

Mu Yu, San-ling Liu, Pei-bei Sun, Hao Pan, Chang-lin Tian, Long-hua Zhang

Open access · bronzeAbstract readReview
In one paragraph

Review in Acta pharmacologica Sinica, 2016. 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
3.1field-weighted citation impact, top 8% 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, 45 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Australian ScorpionBiomolecules · 2020
    Article
  11. Article
  12. Pharmacological modulation of mitochondrial ion channels.British journal of pharmacology · 2019
    Review
  13. Article
  14. Article
  15. A Novel Peptide Restricts Ethanol Modulation of the BK Channel In Vitro and In Vivo.The Journal of pharmacology and experimental therapeutics · 2018
    Article
  16. Cell Cycle Regulation by CaInternational journal of molecular sciences · 2018
    Article
  17. Article
  18. Review
  19. Article
  20. BK Channels Mediate Synaptic Plasticity Underlying Habituation in Rats.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    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

6 authors at 3 institutions in 1 country.

Mu YuHigh Magnetic Field Laboratory, Chinese Academy of Sciences, Hefei 230031, China.
San-ling LiuHigh Magnetic Field Laboratory, Chinese Academy of Sciences, Hefei 230031, China.
Pei-bei SunSchool of Life Sciences, University of Science and Technology of China, Hefei 230027, China.
Hao PanSchool of Life Sciences, University of Science and Technology of China, Hefei 230027, China.
Chang-lin TianHigh Magnetic Field Laboratory, Chinese Academy of Sciences, Hefei 230031, China.
Long-hua ZhangSchool of Life Sciences, University of Science and Technology of China, Hefei 230027, China.
University of Science and Technology of China · CNChinese Academy of Sciences · CNHigh Magnetic Field Laboratory · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Large conductance, Ca(2+)-activated potassium (BK) channels play important roles in the regulation of neuronal excitability and the control of smooth muscle contractions. BK channels can be activated by changes in both the membrane potential and intracellular Ca(2+) concentrations. Here, we provide an overview of the structural and pharmacological properties of BK channel blockers. First, the properties of different venom peptide toxins from scorpions and snakes are described, with a focus on their characteristic structural motifs, including their disulfide bond formation pattern, the binding interface between the toxin and BK channel, and the functional consequence of the blockage of BK channels by these toxins. Then, some representative non-peptide blockers of BK channels are also described, including their molecular formula and pharmacological effects on BK channels. The detailed categorization and descriptions of these BK channel blockers will provide mechanistic insights into the blockade of BK channels. The structures of peptide toxins and non-peptide compounds could provide templates for the design of new channel blockers, and facilitate the optimization of lead compounds for further therapeutic applications in neurological disorders or cardiovascular diseases.

Indexed as

AlkaloidsAnimalsDrug DesignHumansImidazolesLarge-Conductance Calcium-Activated Potassium ChannelsPeptidesPotassium Channel BlockersQuinolinesScorpion VenomsSnake VenomsAlkaloidsImidazolesLarge-Conductance Calcium-Activated Potassium ChannelsPeptidesPotassium Channel BlockersQuinolinesScorpion VenomsSnake Venoms

Identifiers

PMID26725735
PMCPMC4722972
OpenAlexW2415839365

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.