Evidence map›Paper›PMID 12466229›Full record

ArticleBritish journal of pharmacology2002

Inhibitory mechanism of xestospongin-C on contraction and ion channels in the intestinal smooth muscle.

Hiroshi Ozaki, Masatoshi Hori, Yoon-Sun Kim, Seong-Chun Kwon, Duck-Sun Ahn, Hiroshi Nakazawa, Motomasa Kobayashi, Hideaki Karaki

Open access · greenAbstract read
In one paragraph

Article in British journal of pharmacology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

21 citing papers in PubMed, 47 citations in OpenAlex.

  1. Pacemaking in the lymphatic system.The Journal of physiology · 2026
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  7. Pulsed infrared releases CaJournal of neurophysiology · 2018
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  12. M1-muscarinic receptors promote fear memory consolidation via phospholipase C and the M-current.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
    Article
  13. Inositol trisphosphate receptors in smooth muscle cells.American journal of physiology. Heart and circulatory physiology · 2012
    Review
  14. Article
  15. Article
  16. Forskolin Changes the Relationship between Cytosolic Ca and Contraction in Guinea Pig Ileum.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2009
    Article
  17. Article
  18. 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

8 authors at 3 institutions in 2 countries.

Hiroshi OzakiDepartment of Veterinary Pharmacology, Graduate School of Agriculture and Life Sciences, The University of Tokyo, Tokyo 113-8657, Japan. aozaki@mail.ecc.u-tokyo.ac.jp
Masatoshi Hori
Yoon-Sun Kim
Seong-Chun Kwon
Duck-Sun Ahn
Hiroshi Nakazawa
Motomasa Kobayashi
Hideaki Karaki
The University of Tokyo · JPYonsei University · KROsaka University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

1. Xestospongin-C isolated from a marine sponge, Xestospongia sp., has recently been shown to be a membrane-permeable IP(3) receptor inhibitor. In this study we examined the effects of this compound on smooth muscle from guinea-pig ileum. 2. In guinea-pig ileum permeabilized with alpha-toxin, xestospongin-C (3 microM) inhibited contractions induced by Ca(2+) mobilized from sarcoplasmic reticulum (SR) with IP(3) or carbachol with GTP, but not with caffeine. 3. In intact smooth muscle tissue, xestospongin-C (3-10 microM) inhibited carbachol- and high-K+-induced increases in [Ca(2+)](i) and contractions at sustained phase. 4. It also inhibited voltage-dependent inward Ba(2+) currents in a concentration-dependent manner with an IC(50) of 0.63 microM. Xestospongin-C (3-10 microM) had no effect on carbachol-induced inward Ca(2+) currents via non-selective cation channels; but it did reduce voltage-dependent K+ currents in a concentration-dependent manner with an IC(50) of 0.13 microM. 5. These results suggest that xestospongin-C inhibits the IP(3) receptor but not the ryanodine receptor in smooth muscle SR membrane. In intact smooth muscle cells, however, xestospongin-C appears to inhibit voltage-dependent Ca(2+) and K+ currents at a concentration range similar to that at which it inhibits the IP(3) receptor. Xestospongin-C is a selective blocker of the IP(3) receptor in permeabilised cells but not in cells with intact plasma membrane.

Indexed as

AnimalsCalcium ChannelsDose-Response Relationship, DrugGuinea PigsIleumInositol 1,4,5-Trisphosphate ReceptorsIon ChannelsMacrocyclic CompoundsMaleMuscle ContractionMuscle, SmoothOxazolesReceptors, Cytoplasmic and NuclearCalcium ChannelsInositol 1,4,5-Trisphosphate ReceptorsIon ChannelsMacrocyclic CompoundsOxazolesReceptors, Cytoplasmic and Nuclearxestospongin A

Identifiers

PMID12466229
PMCPMC1573613
OpenAlexW2042474871

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.