Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5814090 | Neuropharmacology | 2015 | 12 Pages |
Abstract
The affinity of MRZ-99030 to Aβ1-42 determined by SPR was 28.4 nM but the ratio of compound to Aβ is also important: a 10-20 fold excess of MRZ-99030 over Aβ is probably required for effective modulation of protein/protein interactions. For example, in glaucoma, assuming a maximal Aβ concentration of 1-15 nM in the retina, up to 150 nM MRZ-99030 could be required at the protein target. In line with this consideration, MRZ-99030 was able to prevent Aβ-induced toxicity on PC12 cells, retinal ganglion cells and retinal pigment epithelium cells when present at a 10-20 fold stoichiometric excess over Aβ. Moreover, in vivo studies demonstrate the neuroprotective potential of MRZ-99030 after systemic and topical administration in animal models of Alzheimer's disease and glaucoma/AMD respectively.
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Authors
Christopher G. Parsons, Maarten Ruitenberg, Christine E. Freitag, Kamila Sroka-Saidi, Hermann Russ, Gerhard Rammes,