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T. A. Lanz, M. J. Karmilowicz, K. M. Wood, N. Pozdnyakov, P. Du, M. A. Piotrowski, T. M. Brown, C. E. Nolan, K. E. Richter, J. E. Finley, Q. Fei, C. F. Ebbinghaus, Y. L. Chen, D. K. Spracklin, B. Tate, K. F. Geoghegan, L. F. Lau, D. D. Auperin and J. B. Schachter, “Concentration-Dependent Modulation of Amyloid-β in Vivo and in Vitro Using the Gamma-Secretase Inhibitor, LY-450139,” Journal of Pharmacology and Experimental Therapeutics, Vol. 319, No. 2, 2006, pp. 924-933. doi:10.1124/jpet.106.110700

has been cited by the following article:

• TITLE: Pharmacological Assessment of γ-Secretase Activity from Rodent and Human Brain

  AUTHORS: Christine E. Oborski, Rathna Iyer, Bruce A. Maguire, Gary Bora, Kevin Atchison, Nikolay Pozdnyakov, Kathleen Wood, Christine Parker, Timothy A. Subashi, Martin Pettersson, Douglas S. Johnson, Kelly R. Bales

  KEYWORDS: Alzheimer’s Disease; Amyloid Precursor Protein; Aβ; γ-Secretase; Pharmacology

  JOURNAL NAME: Neuroscience and Medicine, Vol.3 No.2, June 12, 2012

  ABSTRACT: γ-Secretase is involved in the final processing of the amyloid precursor protein into a heterogeneous pool of β-amyloid (Aβ) peptides. Current Alzheimer’s disease drug discovery efforts include targeting γ-secretase activity in brain to attenuate production of the neurotoxic Aβ species. The resulting pharmacology may be affected by species-specific differences in the γ-secretase core complex or its associated proteins. Therefore, we utilized partially purified γ-secretase membranes derived from the brains of different species, including human cortex, to quantitatively assess the de novo production of both Aβ42 and Aβ40 following treatment with known γ-secretase inhibitors and modulators. We determined that the inhibitory activity of a Notch-1 sparing γ-secretase inhibitor and the modulatory activity of two classes of γ-secretase modulators were equipotent at affecting the production of Aβ across rodent and human brain membrane preparations. Additionally, the observed modulator-specific Aβ profile in isolated brain membranes across species was similar to that observed in HeLa cell membranes, and the brain and CSF of guinea pigs following oral administration. By utilizing rapidly purified γ-secretase, we were able to probe and compare the complex pharmacology of γ-secretase in the brain across common rodent species and human cortex.