Evidence map›Paper›PMID 15911617›Full record

ArticleThe Journal of biological chemistry2005

Metabolism and transactivation activity of 13,14-dihydroretinoic acid.

Alexander R Moise, Vladimir Kuksa, William S Blaner, Wolfgang Baehr, Krzysztof Palczewski

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

26 citing papers in PubMed, 57 citations in OpenAlex.

  1. Stereoselective Synthesis of (The Journal of organic chemistry · 2025
    Article
  2. Article
  3. Immunometabolic effects ofImmunometabolism (Cobham, Surrey) · 2024
    Review
  4. Article
  5. Review
  6. Carotenoid modifying enzymes in metazoans.Methods in enzymology · 2022
    Article
  7. Article
  8. Frontiers in cell and developmental biology · 2021
    Article
  9. The role of β-carotene and vitamin A in atherogenesis: Evidences from preclinical and clinical studies.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2020
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. The retinaldehyde reductase DHRS3 is essential for preventing the formation of excess retinoic acid during embryonic development.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2013
    Article
  15. Review
  16. Review
  17. Retinoids for treatment of retinal diseases.Trends in pharmacological sciences · 2010
    Review
  18. Increased adiposity in the retinol saturase-knockout mouse.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2010
    Article
  19. Review
  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

5 authors at 3 institutions in 1 country.

Alexander R MoiseDepartment of Ophthalmology, University of Washington, Seattle, Washington 98195, USA.
Vladimir Kuksa
William S Blaner
Wolfgang Baehr
Krzysztof Palczewski
University of Washington · USColumbia University · USUniversity of Utah · US

Funding

REGULATION OF RHODOPSIN KINASE AND GUANYLATE CYCLASER01EY008061 · NEI · UNIVERSITY OF WASHINGTON · PI PALCZEWSKI, KRZYSZTOF · 1994 to 2014
$9.5M
RETINAL PHOTORECEPTOR CYCLIC GMP PHOSPHODIESTERASER01EY008123 · NEI · UNIVERSITY OF UTAH · PI BAEHR, WOLFGANG · 1990 to 2019
$7.8M
RHODOPSIN KINASE: REGULATION, FUNCTION AND STRUCTURER29EY008061 · NEI · UNIVERSITY OF WASHINGTON · PI PALCZEWSKI, KRZYSZTOF NMI · 1989 to 1993
–
NEI NIH HHS EY08061NEI NIH HHS EY08123NEI NIH HHS R01 EY008061NEI NIH HHS R01 EY008123
6 · The paper itself

Abstract

The metabolism of vitamin A is a highly regulated process that generates essential mediators involved in the development, cellular differentiation, immunity, and vision of vertebrates. Retinol saturase converts all-trans-retinol to all-trans-13,14-dihydroretinol (Moise, A. R., Kuksa, V., Imanishi, Y., and Palczewski, K. (2004) J. Biol. Chem. 279, 50230-50242). Here we demonstrate that the enzymes involved in oxidation of retinol to retinoic acid and then to oxidized retinoic acid metabolites are also involved in the synthesis and oxidation of all-trans-13,14-dihydroretinoic acid. All-trans-13,14-dihydroretinoic acid can activate retinoic acid receptor/retinoid X receptor heterodimers but not retinoid X receptor homodimers in reporter cell assays. All-trans-13,14-dihydroretinoic acid was detected in vivo in Lrat-/- mice supplemented with retinyl palmitate. Thus, all-trans-13,14-dihydroretinoic acid is a naturally occurring retinoid and a potential ligand for nuclear receptors. This new metabolite can also be an intermediate in a retinol degradation pathway or it can serve as a precursor for the synthesis of bioactive 13,14-dihydroretinoid metabolites.

Indexed as

Transcriptional ActivationAldehydesAnimalsCatalysisCell LineChromatography, High Pressure LiquidCloning, MolecularCytochrome P-450 Enzyme SystemDimerizationDNA, ComplementaryElectrophoresis, Polyacrylamide GelGenes, ReporterHumansHydrolysisLiverMice13,14-dihydroretinoic acidAldehydesCytochrome P-450 Enzyme SystemDNA, ComplementaryOxygenRetinoic Acid 4-HydroxylaseRetinoidsRetinoid X ReceptorsTretinoinVitamin A

Identifiers

PMID15911617
PMCPMC1352314
OpenAlexW1968222382

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.