AI Article Synopsis

  • Retinitis Pigmentosa (RP) is an inherited eye disease affecting about 1 in 4000 people worldwide, often leading to vision loss.
  • Researchers tested various drugs on a zebrafish model of RP to find potential treatments, focusing on the impact of oxidative stress on the disease.
  • They discovered that the FDA-approved beta-blocker carvedilol improved visual function and increased rod cell numbers in the zebrafish, suggesting it could be repurposed for treating autosomal dominant RP in humans.

Article Abstract

Retinitis Pigmentosa (RP) is a mostly incurable inherited retinal degeneration affecting approximately 1 in 4000 individuals globally. The goal of this work was to identify drugs that can help patients suffering from the disease. To accomplish this, we screened drugs on a zebrafish autosomal dominant RP model. This model expresses a truncated human rhodopsin transgene (Q344X) causing significant rod degeneration by 7 days post-fertilization (dpf). Consequently, the larvae displayed a deficit in visual motor response (VMR) under scotopic condition. The diminished VMR was leveraged to screen an ENZO SCREEN-WELL REDOX library since oxidative stress is postulated to play a role in RP progression. Our screening identified a beta-blocker, carvedilol, that ameliorated the deficient VMR of the RP larvae and increased their rod number. Carvedilol may directly on rods as it affected the adrenergic pathway in the photoreceptor-like human Y79 cell line. Since carvedilol is an FDA-approved drug, our findings suggest that carvedilol can potentially be repurposed to treat autosomal dominant RP patients.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8169685PMC
http://dx.doi.org/10.1038/s41598-021-89482-zDOI Listing

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