Evidence map›Paper›PMID 19393691›Full record

ReviewPharmacology & therapeutics2009

Pharmacological profiles of alpha 2 adrenergic receptor agonists identified using genetically altered mice and isobolographic analysis.

Carolyn A Fairbanks, Laura S Stone, George L Wilcox

Abstract readReview
In one paragraph

Review in Pharmacology & therapeutics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

40 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Article
  8. Classics in Chemical Neuroscience: Medetomidine.ACS chemical neuroscience · 2024
    Review
  9. Review
  10. Article
  11. Article
  12. Rapid Recovery and Short Duration Anesthesia after Low Dose Ketamine and High Dose Dexmedetomidine in Rhesus Macaques (Journal of the American Association for Laboratory Animal Science : JAALAS · 2021
    Article
  13. Role of α2-Adrenoceptor Subtypes in Suppression of L-Type CaInternational journal of molecular sciences · 2021
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Spinal αBritish journal of pharmacology · 2019
    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

3 authors.

Carolyn A FairbanksDepartment of Pharmaceutics, College of Pharmacy, University of Minnesota, Minneapolis, MN 55455, USA.
Laura S Stone
George L Wilcox

Funding

Mechanisms of Opioid Receptor InteractionsR01DA015438 · NIDA · UNIVERSITY OF MINNESOTA TWIN CITIES · PI WILCOX, GEORGE LATIMER · 2004 to 2014
$3.3M
Peripheral interactions of opioid-adrenergic analgesicsR21DA015735 · NIDA · UNIVERSITY OF MINNESOTA TWIN CITIES · PI WILCOX, GEORGE LATIMER · 2002 to 2003
$297k
G-Protein Coupled Receptor Oligomerization in the CNSR21DA017075 · NIDA · UNIVERSITY OF MINNESOTA TWIN CITIES · PI STONE, LAURA S · 2003 to 2004
$297k
NIDA NIH HHS R01 DA015438NIDA NIH HHS R21 DA015735NIDA NIH HHS R21 DA017075
6 · The paper itself

Abstract

Endogenous, descending noradrenergic fibers impose analgesic control over spinal afferent circuitry mediating the rostrad transmission of pain signals. These fibers target alpha 2 adrenergic receptors (alpha(2)ARs) on both primary afferent terminals and secondary neurons, and their activation mediates substantial inhibitory control over this transmission, rivaling that of opioid receptors which share a similar pattern of distribution. The terminals of primary afferent nociceptive neurons and secondary spinal dorsal horn neurons express alpha(2A)AR and alpha(2C)AR subtypes, respectively. Spinal delivery of these agents serves to reduce their side effects, which are mediated largely at supraspinal sites, by concentrating the drugs at the spinal level. Targeting these spinal alpha(2)ARs with one of five selective therapeutic agonists, clonidine, dexmedetomidine, brimonidine, ST91 and moxonidine, produces significant antinociception that can work in concert with opioid agonists to yield synergistic antinociception. Application of several genetically altered mouse lines had facilitated identification of the primary receptor subtypes that likely mediate the antinociceptive effects of these agents. This review provides first an anatomical description of the localization of the three subtypes in the central nervous system, second a detailed account of the pharmacological history of each of the six primary agonists, and finally a comprehensive report of the specific interactions of other GPCR agonists with each of the six principal alpha(2)AR agonists featured.

Indexed as

Adrenergic alpha-2 Receptor AgonistsAdrenergic alpha-AgonistsAlgorithmsAnalgesicsAnimalsDose-Response Relationship, DrugDrug SynergismInjections, SpinalMiceMice, Mutant StrainsPainPain ThresholdReceptors, Adrenergic, alpha-2Receptors, OpioidSpinal CordAdrenergic alpha-2 Receptor AgonistsAdrenergic alpha-AgonistsAnalgesicsReceptors, Adrenergic, alpha-2Receptors, Opioid

Identifiers

PMID19393691
PMCPMC2724647

What OpenQuestion holds

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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.