Evidence map›Paper›PMID 19500430›Full record

ArticleVisual neuroscience

Beta-ionone activates and bleaches visual pigment in salamander photoreceptors.

Tomoki Isayama, S L McCabe England, R K Crouch, A L Zimmerman, C L Makino

Abstract read
In one paragraph

Article in Visual neuroscience. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.3field-weighted citation impact, top 40% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. β-Ionone facilitates ex vivo airway smooth muscle relaxation via extraocular opsin-3 light receptor activation.American journal of physiology. Lung cellular and molecular physiology · 2025
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. 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.

Tomoki IsayamaDepartment of Ophthalmology, Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, Massachusetts 02114, USA. tomoki_isayama@meei.harvard.edu
S L McCabe England
R K Crouch
A L Zimmerman
C L Makino
Brown University · USHarvard University · USSmith-Kettlewell Eye Research Institute · US

Funding

P30 Core Grant for Vision ResearchP30EY014104 · NEI · MASSACHUSETTS EYE AND EAR INFIRMARY · PI Eric A Pierce · 2002 to 2026
$15.1M
SYNTHETIC RETINAL PIGMENTS AND BINDING PROTEINSR01EY004939 · NEI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI CROUCH, ROSALIE K · 1985 to 2011
$4.2M
Multiple Ligand Binding Sites of Rod and Cone OpsinsR01EY011358 · NEI · MASSACHUSETTS EYE AND EAR INFIRMARY · PI MAKINO, CLINT L · 2002 to 2011
$2.9M
PROPERTIES OF LIGHT-MODULATED ION CHANNELS IN THE RETINAR01EY007774 · NEI · BROWN UNIVERSITY · PI ZIMMERMAN, ANITA L · 1988 to 2005
$1.8M
Light Adaptation in Vertebrate Rod PhotoreceptorsR01EY012944 · NEI · MASSACHUSETTS EYE AND EAR INFIRMARY · PI MAKINO, CLINT L · 2001 to 2005
$1.3M
Core Resources for Vision Research at MUSCR24EY014793 · NEI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI CROSSON, CRAIG E. · 2003 to 2007
$1.0M
REGULATION OF PHOTORECEPTORS SPECTRAL SENSITIVITYR29EY011358 · NEI · MASSACHUSETTS EYE AND EAR INFIRMARY · PI MAKINO, CLINT L · 1997 to 2001
$227k
NEI NIH HHS EY014104NEI NIH HHS EY014793NEI NIH HHS EY04939NEI NIH HHS EY07774NEI NIH HHS EY11358NEI NIH HHS EY12944NEI NIH HHS P30 EY014104NEI NIH HHS R01 EY004939NEI NIH HHS R01 EY007774NEI NIH HHS R01 EY011358NEI NIH HHS R01 EY012944NEI NIH HHS R24 EY014793NEI NIH HHS R29 EY011358
6 · The paper itself

Abstract

Vision begins with photoisomerization of 11-cis retinal to the all-trans conformation within the chromophore-binding pocket of opsin, leading to activation of a biochemical cascade. Release of all-trans retinal from the binding pocket curtails but does not fully quench the ability of opsin to activate transducin. All-trans retinal and some other analogs, such as beta-ionone, enhance opsin's activity, presumably on binding the empty chromophore-binding pocket. By recording from isolated salamander photoreceptors and from patches of rod outer segment membrane, we now show that high concentrations of beta-ionone suppressed circulating current in dark-adapted green-sensitive rods by inhibiting the cyclic nucleotide-gated channels. There were also decreases in circulating current and flash sensitivity, and accelerated flash response kinetics in dark-adapted blue-sensitive (BS) rods and cones, and in ultraviolet-sensitive cones, at concentrations too low to inhibit the channels. These effects persisted in BS rods even after incubation with 9-cis retinal to ensure complete regeneration of their visual pigment. After long exposures to high concentrations of beta-ionone, recovery was incomplete unless 9-cis retinal was given, indicating that visual pigment had been bleached. Therefore, we propose that beta-ionone activates and bleaches some types of visual pigments, mimicking the effects of light.

Indexed as

AnimalsCaudataCyclic Nucleotide-Gated Cation ChannelsDark AdaptationDose-Response Relationship, DrugElectric ConductivityIn Vitro TechniquesKineticsLarvaMembranesNorisoprenoidsPhotoreceptor Cells, VertebrateRetinal PigmentsRetinal Rod Photoreceptor CellsRod Cell Outer SegmentTime Factorsbeta-iononeCyclic Nucleotide-Gated Cation ChannelsNorisoprenoidsRetinal Pigments

Identifiers

PMID19500430
PMCPMC3220273
OpenAlexW2099129526

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.