Evidence map›Paper›PMID 10694209›Full record

ArticleBritish journal of pharmacology2000

The peripheral antinociceptive effect induced by morphine is associated with ATP-sensitive K(+) channels.

A R Rodrigues, I D Duarte

Open access · bronzeAbstract read
In one paragraph

Article in British journal of pharmacology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

39 citing papers in PubMed, 181 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Modulation of SUR1 KInternational journal of molecular sciences · 2019
    Article
  8. Antinociceptive effect of PnTx4(5-5), a peptide fromThe journal of venomous animals and toxins including tropical diseases · 2019
    Article
  9. Article
  10. Role of L-arginine/NO/cGMP/KIranian journal of basic medical sciences · 2018
    Article
  11. Article
  12. Article
  13. Review
  14. Antinociceptive Activities of the Methanolic Extract of the Stem Bark ofEvidence-based complementary and alternative medicine : eCAM · 2017
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Skin vasodilation and analgesic effect of a topical nitric oxide-releasing hydrogel.Journal of materials science. Materials in medicine · 2013
    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

2 authors at 1 institution in 1 country.

A R RodriguesDepartment of Pharmacology, Institute of Biological Sciences, UFMG, 31.270.100, Belo Horizonte, Brazil.
I D Duarte
Universidade Federal de Minas Gerais · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The effect of several K(+) channel blockers such as glibenclamide, tolbutamide, charybdotoxin (ChTX), apamin, tetraethylammonium (TEA), 4-aminopyridine (4-AP) and cesium on the peripheral antinociceptive effect of morphine was evaluated by the paw pressure test in Wistar rats. The intraplantar administration of a carrageenan suspension (250 microg) resulted in an acute inflammatory response and a decreased threshold to noxious pressure. Morphine administered locally into the paw (25, 50, 100 and 200 microg) elicited a dose-dependent antinociceptive effect which was demonstrated to be mediated by a peripheral site up to the 100 microg dose. The selective blockers of ATP-sensitive K(+) channels glibenclamide (20, 40 and 80 microg paw(-1)) and tolbutamide (40, 80 and 160 microg paw(-1)) antagonized the peripheral antinociception induced by morphine (100 microg paw(-1)). This effect was unaffected by ChTX (0. 5, 1.0 and 2.0 microg paw(-1)), a large conductance Ca(2+)-activated K(+) channel blocker, or by apamin (2.5, 5.0 and 10.0 microg paw(-1)), a selective blocker of a small conductance Ca(2+)-activated K(+) channel. Intraplantar administration of the non-specific K(+) channel blockers TEA (160, 320 and 640 microg), 4-AP (10, 50 and 100 microg) and cesium (125, 250 and 500 microg) also did not modify the peripheral antinociceptive effect of morphine. These results suggest that the peripheral antinociceptive effect of morphine may result from activation of ATP-sensitive K(+) channels, which may cause a hyperpolarization of peripheral terminals of primary afferents, leading to a decrease in action potential generation. In contrast, large conductance Ca(2+)-activated K(+) channels, small conductance Ca(2+)-activated K(+) channels as well as voltage-dependent K(+) channels appear not to be involved in this transduction pathway. British Journal of Pharmacology (2000) 129, 110 - 114

Indexed as

Potassium Channel BlockersPotassium ChannelsPotassium Channels, Calcium-Activated4-AminopyridineAnalgesics, OpioidAnimalsApaminATP-Binding Cassette TransportersCesiumCharybdotoxinDrug InteractionsHyperalgesiaHypoglycemic AgentsKATP ChannelsLarge-Conductance Calcium-Activated Potassium ChannelsMale4-AminopyridineAnalgesics, OpioidApaminATP-Binding Cassette TransportersCesiumCharybdotoxinHypoglycemic AgentsKATP ChannelsLarge-Conductance Calcium-Activated Potassium ChannelsMorphinePotassium Channel BlockersPotassium ChannelsPotassium Channels, Calcium-ActivatedPotassium Channels, Inwardly RectifyingTetraethylammoniumuK-ATP-1 potassium channel

Identifiers

PMID10694209
PMCPMC1621137
OpenAlexW1999908521

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.