Evidence map›Paper›PMID 20578038›Full record

ArticleGlia2010

Morphine induces the release of CCL5 from astrocytes: potential neuroprotective mechanism against the HIV protein gp120.

Valeriya Avdoshina, Francesca Biggio, Guillermo Palchik, Lee A Campbell, Italo Mocchetti

Abstract read
In one paragraph

Article in Glia, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
–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

51 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Modulation of OPRM1 Alternative Splicing by Morphine and HIV-1 Nef.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2022
    Article
  6. Article
  7. Review
  8. Chemokine CCL5 promotes robust optic nerve regeneration and mediates many of the effects of CNTF gene therapy.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  9. Opioid and neuroHIV Comorbidity - Current and Future Perspectives.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2020
    Review
  10. Article
  11. Review
  12. Article
  13. Entanglement of CCR5 and Alzheimer's Disease.Frontiers in aging neuroscience · 2019
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. HIV-1 Proteins Influence Novelty-Seeking Behavior and Alter Region-Specific Transcriptional Responses to Chronic Nicotine Treatment in HIV-1Tg Rats.Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco · 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

5 authors.

Valeriya AvdoshinaDepartment of Neuroscience, Georgetown University Medical Center, Washington, DC 20057, USA.
Francesca Biggio
Guillermo Palchik
Lee A Campbell
Italo Mocchetti

Funding

HIV drug abusers, polymorphisms and brain plasticityR01DA026174 · NIDA · GEORGETOWN UNIVERSITY · PI MOCCHETTI, ITALO · 2008 to 2012
$1.8M
TRAINING PROGRAM IN DRUG ABUSET32DA007291 · NIDA · GEORGETOWN UNIVERSITY · PI BAYER, BARBARA M · 1992 to 2009
$1.4M
NIDA NIH HHS DA026174NIDA NIH HHS R01 DA026174NIDA NIH HHS T32 DA007291
6 · The paper itself

Abstract

A number of human immunodeficiency virus type-1 (HIV) positive subjects are also opiate abusers. These individuals are at high risk to develop neurological complications. However, little is still known about the molecular mechanism(s) linking opiates and HIV neurotoxicity. To learn more, we exposed rat neuronal/glial cultures prepared from different brain areas to opiate agonists and HIV envelope glycoproteins gp120IIIB or BaL. These strains bind to CXCR4 and CCR5 chemokine receptors, respectively, and promote neuronal death. Morphine did not synergize the toxic effect of gp120IIIB but inhibited the cytotoxic property of gp120BaL. This effect was blocked by naloxone and reproduced by the mu opioid receptor agonist DAMGO. To examine the potential mechanism(s) of neuroprotection, we determined the effect of morphine on the release of chemokines CCL5 and CXCL12 in neurons, astrocytes, and microglia cultures. CCL5 has been shown to prevent gp120BaL neurotoxicity while CXCL12 decreases neuronal survival. Morphine elicited a time-dependent release of CCL5 but failed to affect the release of CXCL12. This effect was observed only in primary cultures of astrocytes. To examine the role of endogenous CCL5 in the neuroprotective activity of morphine, mixed cerebellar neurons/glial cells were immunoneutralized against CCL5 prior to morphine and gp120 treatment. In these cells the neuroprotective effect of opiate agonists was blocked. Our data suggest that morphine may exhibit a neuroprotective activity against M-tropic gp120 through the release of CCL5 from astrocytes.

Indexed as

Analgesics, OpioidAnimalsAnimals, NewbornAstrocytesCells, CulturedCell SurvivalCerebellumChemokine CCL5CytarabineEnkephalin, Ala(2)-MePhe(4)-Gly(5)-Enzyme-Linked Immunosorbent AssayGene Expression RegulationHippocampusHIV Envelope Protein gp120MorphineNarcoticsAnalgesics, OpioidChemokine CCL5CytarabineEnkephalin, Ala(2)-MePhe(4)-Gly(5)-HIV Envelope Protein gp120MorphineNarcotics

Identifiers

PMID20578038
PMCPMC2919594

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Registered trials

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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.