Effects of Long-Term Administration of 9-cis-Retinyl Acetate on Visual Function in Mice
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PURPOSE: Long-term effects of treatment with 9-cis-retinyl acetate (9-cis-R-Ac), an artificial retinoid prodrug, were tested on changes in rod and cone visual functions in mice. METHODS: The acetyl ester of the functional geometric chromophore 9-cis-retinal was delivered by oral gavage to C57BL/6 female mice. In initial experiments, 10-month-old mice were used for the single treatment with 9-cis-R-Ac or the control vehicle. In long-term experiments, 4-month-old mice were treated with 9-cis-R-Ac monthly for 6 and 10 months. Photoreceptor status was evaluated by various electroretinographic (ERG) techniques, retinoid analyses, and retinal morphology. Opsin, the predicted target of oxidized 9-cis-R-Ac, was purified and its chromophore was characterized. RESULTS: Age-related changes observed in vehicle-treated mice at 10 months of age, compared with those in 4-month-old mice, included a progressive decline in ERG responses, such as a decreased rate of dark adaptation and a lowered rhodopsin/opsin ratio. Administration of 9-cis-R-Ac increased the rhodopsin regeneration ratio, and improved ERG responses and dark adaptation. Compared with vehicle-treated control animals, 10- and 14-month-old mice treated monthly with 9-cis-R-Ac for 6 or 10 months exhibited improved dark adaptation. In 14-month-old mice treated monthly, changes in the expression of retina-specific genes in the eye were detected by mRNA expression profiling, but no significant effects in gene expression were detected in the liver and kidney. CONCLUSIONS: Deteriorating photoreceptor function documented in mice at 10 and 14 versus 4 months of age was improved significantly by long-term, monthly administration of 9-cis-R-Ac. These findings suggest a potential therapeutic approach to prevent age-related retinal dysfunction.
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The toxicity of all-trans-retinal could be a major contributor to retinal degeneration in several human diseases, including Stargardt disease.
“The toxicity of all-trans-retinal could be a major contributor to retinal degeneration in several human diseases, including Stargardt disease.318,401,570”
From Chemistry of the Retinoid (Visual) Cycle (2014) · cites this paper as [570]
The Discussion (no page provided) says that a buildup of all-trans-retinal after light exposure has been suggested to lead to accumulation of potentially toxic A2E. It does not say that all-trans-retinal’s own toxicity is a major contributor to retinal degeneration in several human diseases, including Stargardt disease; Stargardt appears in the references, not in that proposed mechanism. (LLM, conf=0.82)
Experimental — accuracy not yet measuredOral delivery of 9-cis-retinal overcomes blockage in production of 11-cis-retinal.
“Thus, blockage in production of 11-cis-retinal was overcome with oral delivery of another photosensitive but chemically more stable retinoid, 9-cis-retinal (Figure 36)567−571”
From Chemistry of the Retinoid (Visual) Cycle (2014) · cites this paper as [570]
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References 64 · Cited by 27
- Authors
- Maeda, T., Maeda, A., Leahy, P., Saperstein, D. A., & Palczewski, K.
- Affiliations
- From the Departments of Pharmacology and2Ophthalmology and Visual Science, and the
- From the Departments of Pharmacology and
- Case Comprehensive Cancer Center (US)
- University of Washington (US)
- Venue
- Investigative Opthalmology & Visual Science
- Published
- 2009-01-01
- Volume
- 50
- Issue
- 1
- Pages
- 322
- ISSN
- 0146-0404 (ISSN-L)
- 1552-5783
- PMC
- PMC2615069
- OpenAlex
- W2148585498
- Cited by
- 27
- References
- 64
- Citations by year
- 2026: 1 · 2025: 2 · 2023: 1 · 2022: 1 · 2021: 1 · 2020: 1 · 2019: 1 · 2018: 1 · 2017: 1 · 2016: 3 · 2015: 2 · 2013: 1 · 2012: 3
- FWCI
- 1.46
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Investigative Ophthalmology & Visual Science (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Eye Institute (EY 09339, P30EY011373, R01EY009339)
- National Cancer Institute (P30CA043703)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Retinal Development and Disorders
- Health Sciences › Medicine › Ophthalmology › Retinal Diseases and Treatments
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Retinoids in leukemia and cellular processes
- Keywords
- 9-cis-retinal, photoreceptor function, dark adaptation, rhodopsin regeneration, opsin, retinal gene expression, long-term oral administration, electroretinogram
- MeSH terms
- Retinyl Esters, Administration, Oral, Aging, Animals, Dark Adaptation, Diterpenes, Electroretinography, Female, Mice, Inbred C57BL, Photic Stimulation, Prodrugs, Retinoids, Rhodopsin, RNA, Vitamin A, Photoreceptor Cells, Vertebrate, Gene Expression Profiling, Microarray Analysis, Mice, Opsins
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