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Ripasudil does not induce phospholipid accumulation in human corneal epithelial cells
Fumiko Tazoe1, Yuichiro Watanabe1, Noriyuki Inoue1
1Tokyo New Drug Research Laboratories, Kowa Company, Ltd., Tokyo, Japan.
Ripasudil, a novel glaucoma drug, is unlikely to cause cornea verticillata. Unlike netarsudil, ripasudil did not induce intracellular phospholipid accumulation in corneal cells, suggesting a lower risk of this adverse effect.
Area of Science:
- Ophthalmology
- Pharmacology
- Cell Biology
Background:
- Rho-associated coiled-coil-containing protein kinase (ROCK) inhibitors are a new class of glaucoma drugs.
- Netarsudil, a ROCK inhibitor, can cause cornea verticillata, a rare corneal condition.
Purpose of the Study:
- To investigate if ripasudil, another ROCK inhibitor, induces cornea verticillata.
- To compare the effects of ripasudil, netarsudil, and Y-27632 on corneal cells.
Main Methods:
- Corneal cell lines (CHO-K1, HCE-T) and primary human corneal epithelial cells (HCEC-2) were treated with varying concentrations of ripasudil, netarsudil, or Y-27632.
- Intracellular phospholipid levels were measured to assess drug-induced phospholipidosis.
Main Results:
- Ripasudil and Y-27632 did not affect intracellular phospholipid levels.
- Netarsudil treatment led to intracellular phospholipid accumulation.
- Netarsudil shares chemical similarities with cationic amphiphilic drugs known to cause phospholipidosis, unlike ripasudil and Y-27632.
Conclusions:
- Ripasudil is unlikely to induce cornea verticillata due to its chemical structure.
- The findings suggest a favorable safety profile for ripasudil regarding corneal adverse effects.
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