Evidence map›Paper›PMID 21569838›Full record

ArticleBrain, behavior, and immunity2011

The effect of gp120 on morphine's antinociceptive and neurophysiological actions.

Xiaohong Chen, Lynn G Kirby, Jonathan Palma, Khalid Benamar, Ellen B Geller, Toby K Eisenstein, Martin W Adler

Abstract read
In one paragraph

Article in Brain, behavior, and immunity, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Reactive Oxygen Species (ROS) are Critical for Morphine Exacerbation of HIV-1 gp120-Induced Pain.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2021
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. HIV-gp120 and physical dependence to buprenorphine.Drug and alcohol dependence · 2015
    Article
  12. Article
  13. Review
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

7 authors at 1 institution in 1 country.

Xiaohong ChenCenter for Substance Abuse Research, Temple University School of Medicine, Philadelphia, PA 19140, USA. chenyang@temple.edu
Lynn G Kirby
Jonathan Palma
Khalid Benamar
Ellen B Geller
Toby K Eisenstein
Martin W Adler
Temple University · US

Funding

Pilot Projects Core (PPC)P30DA013429 · NIDA · TEMPLE UNIV OF THE COMMONWEALTH · PI Anjali M Rajadhyaksha · 2000 to 2026
$34.6M
OPIOIDS, OPIOID RECEPTORS, AND IMMUNE COMPETENCER01DA006650 · NIDA · TEMPLE UNIV OF THE COMMONWEALTH · PI ADLER, MARTIN W · 1991 to 2012
$5.0M
Regulation of Serotonin Circuits in Opiate Addiction and RelapseR01DA020126 · NIDA · TEMPLE UNIV OF THE COMMONWEALTH · PI KIRBY, LYNN G · 2006 to 2010
$1.6M
NIDA NIH HHS DA 06650NIDA NIH HHS DA13429NIDA NIH HHS DA 20126NIDA NIH HHS P30 DA013429NIDA NIH HHS R01 DA006650NIDA NIH HHS R01 DA020126
6 · The paper itself

Abstract

Recently, we have shown that morphine's analgesic activity can be attenuated by chemokines, specifically CCL5 and CXCL12. Because the HIV-1 coat protein, glycoprotein 120 (gp120), binds to the same receptors as do CCL5 and CXCL12, experiments were designed to investigate the effect of gp120 in the brain on antinociception induced by morphine in the cold-water (-3°C) tail-flick (CWT) and hot-plate (+54°C) tests. In addition, mu-opioid-receptor-mediated effects in brain periaqueductal grey (PAG) slices were examined with whole-cell patch-clamp recordings. The results showed that (1) pretreatment with gp120 itself (10, 25, 50, 100 or 133 ng, PAG) had no nociceptive effect in the CWT; (2) pretreatment with gp120 (25 or 100 ng) dose-dependently reduced antinociception induced by subcutaneous (sc) injection of morphine (3 or 6 mg/kg) or PAG injection of morphine (100 ng) in the CWT; (3) a PAG injection of gp120 (133 ng), given 30 min before sc injection of morphine (6 mg/kg), similarly reduced morphine antinociception in the hot-plate test; (4) the inhibitory effect of gp120 on morphine-induced antinociception in the CWT was reversed by AMD3100, an antagonist of CXCR4; (5) pretreatment of slices with gp120 (200 pM) prevented morphine (10 μM)-induced hyperpolarization and reduction of input resistance in PAG neurons. Electrophysiology studies paralleled gp120-induced desensitization of a mu-opioid-receptor-mediated response in PAG neurons at the single-cell level. These studies are the first to demonstrate that the analgesic activity of morphine can be reduced by the presence of gp120 in the PAG and that pretreatment with AMD3100 is able to restore the analgesic effects of morphine.

Indexed as

AnalgesiaAnalgesics, OpioidAnimalsBehavior, AnimalBenzylaminesCold TemperatureCyclamsDose-Response Relationship, DrugDrug InteractionsHeterocyclic CompoundsHIV Envelope Protein gp120Hot TemperatureMaleMembrane PotentialsMorphinePain MeasurementAnalgesics, OpioidBenzylaminesCyclamsHeterocyclic CompoundsHIV Envelope Protein gp120MorphineplerixaforReceptors, CXCR4Receptors, Opioid, mu

Identifiers

PMID21569838
PMCPMC3998826
OpenAlexW1984069777

What OpenQuestion holds

Textmetadata
LicenceTDM
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.