Volume 90 Issue 31 | p. 12 | News of The Week
Issue Date: July 30, 2012

Small Molecule Enables Blind Mice To Respond To Light

Drug Discovery: Research paves way for drug treatment of degenerative blindness
Department: Science & Technology | Collection: Life Sciences
News Channels: Biological SCENE
Keywords: vision, blindness, age-related macular degeneration, retinitis pigmentosa
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Credit: Neuron
This photo is of mice pupils contracted in light after treatment with the small molecule AAQ.
 
Credit: Neuron

Light reflex in the eyes of blind mice can be restored when a potassium channel is unblocked by the light-sensitive small molecule AAQ.

A small-molecule “photoswitch” has enabled blind mice to respond to light (Neuron, DOI: 10.1016/j.neuron.2012.05.022). The work could pave the way for drugs to treat degenerative blindness, which affects 1 in 3,000 people worldwide.

Drugs would be a promising treatment for degenerative blinding diseases such as age-related macular degeneration and retinitis pigmentosa, which ensue when the eye’s light-sensing machinery dies. In contrast, alternative therapies in development, such as prosthetic retinal chips and gene therapy, involve invasive or irreversible intervention.

When researchers injected the chemical into the eyes of genetically modified blind mice and shined light on them, the mice ran away, in a classic avoidance response. Their pupils also contracted in the presence of light, in contrast to remaining dilated without the compound. The effect wore off after 24 hours.

Researchers, including Richard H. Kramer, a neurobiologist at the University of California, Berkeley, and Dirk Trauner, a chemical biologist at the University of Munich, developed the photoswitch molecule, acrylamide-azobenzene-quaternary ammonium, or AAQ. The compound makes an ion channel sensitive to light through a mechanism similar to that of the painkiller lidocaine. In the dark, AAQ is in its trans form, which blocks a potassium channel, but in white light it isomerizes to its cis form, unblocking the channel and allowing specific retinal neurons to fire, sending visual input to the brain.

“It is a very important and cool step forward that may bypass the need for complex viral therapies to deliver genes of frankly unknown efficacies to human eyes,” says Robert E. Marc, director of research at the University of Utah’s department of ophthalmology and visual sciences. “We haven’t had anything like it.”

Trauner says the study provides an exciting first proof of principle, but “we’re still far from knowing whether this could restore vision.”

 
Chemical & Engineering News
ISSN 0009-2347
Copyright © American Chemical Society

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