Evidence map›Paper›PMID 26350413›Full record

ArticleJournal of bioenergetics and biomembranes2015

Morphine stimulates nitric oxide release in human mitochondria.

George B Stefano, Kirk J Mantione, Lismary Capellan, Federico M Casares, Sean Challenger, Rohina Ramin, Joshua M Samuel, Christopher Snyder, Richard M Kream

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of bioenergetics and biomembranes, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-weighted citation impact, top 27% 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

14 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Emerging Roles of Blood-Borne Intact and Respiring Mitochondria as Bidirectional Mediators of Pro- and Anti-Inflammatory Processes.Medical science monitor : international medical journal of experimental and clinical research · 2020
    Article
  7. Review
  8. Review
  9. Review
  10. Microbiome: A Potential Component in the Origin of Mental Disorders.Medical science monitor : international medical journal of experimental and clinical research · 2017
    Review
  11. Reciprocal Evolution of Opiate Science from Medical and Cultural Perspectives.Medical science monitor : international medical journal of experimental and clinical research · 2017
    Review
  12. Glycolytic Coupling to Mitochondrial Energy Production Ensures Survival in an Oxygen Rich Environment.Medical science monitor : international medical journal of experimental and clinical research · 2016
    Review
  13. Review
  14. 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

9 authors at 1 institution in 1 country.

George B StefanoMitoGenetics Research Institute, MitoGenetics LLC, 3 Bioscience Park Drive, Suite 307, Farmingdale, NY, 11735, USA. george.stefano@mitogenetics.com.
Kirk J MantioneMitoGenetics Research Institute, MitoGenetics LLC, 3 Bioscience Park Drive, Suite 307, Farmingdale, NY, 11735, USA.
Lismary CapellanMitoGenetics Research Institute, MitoGenetics LLC, 3 Bioscience Park Drive, Suite 307, Farmingdale, NY, 11735, USA.
Federico M CasaresMitoGenetics Research Institute, MitoGenetics LLC, 3 Bioscience Park Drive, Suite 307, Farmingdale, NY, 11735, USA.
Sean ChallengerMitoGenetics Research Institute, MitoGenetics LLC, 3 Bioscience Park Drive, Suite 307, Farmingdale, NY, 11735, USA.
Rohina RaminMitoGenetics Research Institute, MitoGenetics LLC, 3 Bioscience Park Drive, Suite 307, Farmingdale, NY, 11735, USA.
Joshua M SamuelMitoGenetics Research Institute, MitoGenetics LLC, 3 Bioscience Park Drive, Suite 307, Farmingdale, NY, 11735, USA.
Christopher SnyderMitoGenetics Research Institute, MitoGenetics LLC, 3 Bioscience Park Drive, Suite 307, Farmingdale, NY, 11735, USA.
Richard M KreamMitoGenetics Research Institute, MitoGenetics LLC, 3 Bioscience Park Drive, Suite 307, Farmingdale, NY, 11735, USA.
HistoGenetics (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The expression of morphine by plants, invertebrate, and vertebrate cells and organ systems, strongly indicates a high level of evolutionary conservation of morphine and related morphinan alkaloids as required for life. The prototype catecholamine, dopamine, serves as an essential chemical intermediate in morphine biosynthesis, both in plants and animals. We surmise that, before the emergence of specialized plant and animal cells/organ systems, primordial multi-potential cell types required selective mechanisms to limit their responsiveness to environmental cues. Accordingly, cellular systems that emerged with the potential for recruitment of the free radical gas nitric oxide (NO) as a multi-faceted autocrine/paracrine signaling molecule, were provided with extremely positive evolutionary advantages. Endogenous morphinergic signaling, in concert with NO-coupled signaling systems, has evolved as an autocrine/paracrine regulator of metabolic homeostasis, energy metabolism, mitochondrial respiration and energy production. Basic physiological processes involving morphinergic/NO-coupled regulation of mitochondrial function, with special emphasis on the cardiovascular system, are critical to all organismic survival. Key to this concept may be the phenomenon of mitochondrial enslavement in eukaryotic evolution via endogenous morphine.

Indexed as

Autocrine CommunicationCell LineEnergy MetabolismHumansMitochondriaMorphineNitric OxideParacrine CommunicationMorphineNitric OxideEndogenous morphineMitochondriaNitric oxideNitric oxide synthaseOpiate receptor sub-types

Identifiers

PMID26350413
OpenAlexW1782769616

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.