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      A novel ROCK inhibitor, Y-39983, promotes regeneration of crushed axons of retinal ganglion cells into the optic nerve of adult cats.

      Experimental Neurology
      Amides, pharmacology, Animals, Axons, drug effects, Cats, Cell Survival, Cells, Cultured, Enzyme Inhibitors, administration & dosage, Female, Injections, Intracellular Signaling Peptides and Proteins, antagonists & inhibitors, Male, Nerve Crush, Nerve Fibers, metabolism, pathology, Nerve Regeneration, Neuroglia, Optic Nerve, physiopathology, Protein-Serine-Threonine Kinases, Pyridines, Retina, Retinal Ganglion Cells, Time Factors, Vitreous Body, rho-Associated Kinases

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          Abstract

          We investigated the effect of a novel ROCK inhibitor, Y-39983, on neurite regeneration in vitro and axonal regeneration in the crushed cat optic nerve in vivo. To determine the effective dose for neurite regeneration, retinal pieces were cultured with ROCK inhibitors, Y-39983 or Y-27632, a well-characterized ROCK inhibitor, and the number and length of TUJ-1-positive neurites were evaluated. The greatest number of neurites protruded at a dose of 3-10 microM Y-39983 and at a dose of 10-100 microM Y-27632, respectively. The neurite number at maximum effect of Y-39983 was greater than that of Y-27632. No significant difference was observed between values of neurite length with the inhibitors. Based on this finding, we examined the effect of Y-39983 on axonal regeneration in the crushed optic nerve in vivo. Immediately after crushing the left optic nerve, Y-39983 was injected into the vitreous and the crushed site. An injection of 10 microM Y-39983 induced the crushed axons to regenerate and pass over the crush site. In contrast, very few axons passed beyond the crush site in the optic nerve with phosphate-buffered saline injection. The second injection of 10 microM Y-39983 on day 7 doubled the number of regenerated axons, suggesting that new axons may have entered into the optic nerve after day 7 and that a continuous supply of the drug may make more axons to regenerate.

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