JPET Celsis microsomes equal better data

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


Journal of Pharmacology And Experimental Therapeutics Fast Forward
First published on January 12, 2004; DOI: 10.1124/jpet.103.060715


0022-3565/04/3091-49-55$20.00
JPET 309:49-55, 2004
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
jpet.103.060715v1
309/1/49    most recent
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Lanz, T. A.
Right arrow Articles by Merchant, K. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lanz, T. A.
Right arrow Articles by Merchant, K. M.

NEUROPHARMACOLOGY

Studies of A{beta} Pharmacodynamics in the Brain, Cerebrospinal Fluid, and Plasma in Young (Plaque-Free) Tg2576 Mice Using the {gamma}-Secretase Inhibitor N2-[(2S)-2-(3,5-Difluorophenyl)-2-hydroxyethanoyl]-N1-[(7S)-5-methyl-6-oxo-6,7-dihydro-5H-dibenzo[b,d]azepin-7-yl]-L-alaninamide (LY-411575)

Thomas A. Lanz, John D. Hosley, Wade J. Adams, and Kalpana M. Merchant1

Department of Neurobiology, Pharmacia Corporation, Kalamazoo, Michigan

A previous study by us suggests the utility of cerebrospinal fluid (CSF) and plasma A{beta} as biomarkers of {beta}- or {gamma}-secretase inhibition. The present study characterized further A{beta} pharmacodynamics in these tissues from Tg2576 mice and examined their correlation with brain A{beta} after acute treatment with a potent {gamma}-secretase inhibitor, N2-[(2S)-2-(3,5-difluorophenyl)-2-hydroxyethanoyl]-N1-[(7S)-5-methyl-6-oxo-6,7-dihydro-5H-dibenzo[b,d]azepin-7-yl]-L-alaninamide (LY-411575). A single dose of LY-411575 dose-dependently (0.1–10 mg/kg p.o.) reduced A{beta}(1-40) and A{beta}(1-42) in the CSF and the brain. In contrast, plasma A{beta} levels were increased by 0.1 mg/kg LY-411575 and were followed by a dose-dependent reduction at higher doses. The time courses of A{beta} reduction and recovery were distinct for the three tissues: maximal declines in A{beta} levels were evident by 3 h in the CSF and plasma but not until 9 h in the brain. A recovery in A{beta} levels was underway in the CSF by 9 h and nearly completed by 24 h in all tissues. The differential time courses in the three compartments do not seem to be due to pharmacokinetic factors. Five days of twice-daily treatment with LY-411575 not only sustained the A{beta} reductions in all tissues but also significantly augmented the efficacy in the brain and plasma. The increased efficacy occurred in the absence of compound accumulation and was consistent with the recovery rates in each compartment. Overall, A{beta} in the CSF and not plasma seems to be a better biomarker of brain A{beta} reduction; however, the time course of A{beta} changes needs to be established in clinical studies.


Received September 30, 2003; accepted December 8, 2003.

Address correspondence to: Dr. Thomas A. Lanz, Pfizer, Inc., Eastern Point Road, MS# 8220-4183, Groton, CT 06340. E-mail: thomas.a.lanz{at}pfizer.com




This article has been cited by other articles:


Home page
J. Pharmacol. Exp. Ther.Home page
D. Abramowski, K.-H. Wiederhold, U. Furrer, A.-L. Jaton, A. Neuenschwander, M.-J. Runser, S. Danner, J. Reichwald, D. Ammaturo, D. Staab, et al.
Dynamics of A{beta} Turnover and Deposition in Different {beta}-Amyloid Precursor Protein Transgenic Mouse Models Following {gamma}-Secretase Inhibition
J. Pharmacol. Exp. Ther., November 1, 2008; 327(2): 411 - 424.
[Abstract] [Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
M. E. Goldstein, Y. Cao, T. Fiedler, J. Toyn, L. Iben, D. M. Barten, M. Pierdomenico, J. Corsa, C. V. C. Prasad, R. E. Olson, et al.
Ex Vivo Occupancy of {gamma}-Secretase Inhibitors Correlates with Brain beta-Amyloid Peptide Reduction in Tg2576 Mice
J. Pharmacol. Exp. Ther., October 1, 2007; 323(1): 102 - 108.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
E. Czirr, S. Leuchtenberger, C. Dorner-Ciossek, A. Schneider, M. Jucker, E. H. Koo, C. U. Pietrzik, K. Baumann, and S. Weggen
Insensitivity to Abeta42-lowering Nonsteroidal Anti-inflammatory Drugs and {gamma}-Secretase Inhibitors Is Common among Aggressive Presenilin-1 Mutations
J. Biol. Chem., August 24, 2007; 282(34): 24504 - 24513.
[Abstract] [Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
L. A. Hyde, N. A. McHugh, J. Chen, Q. Zhang, D. Manfra, A. A. Nomeir, H. Josien, T. Bara, J. W. Clader, L. Zhang, et al.
Studies to Investigate the in Vivo Therapeutic Window of the {gamma}-Secretase Inhibitor N2-[(2S)-2-(3,5-Difluorophenyl)-2-hydroxyethanoyl]-N1-[(7S)-5-methyl-6-oxo-6,7-dihydro-5H-dibenzo[b,d]azepin-7-yl]-L-alaninamide (LY411,575) in the CRND8 Mouse
J. Pharmacol. Exp. Ther., December 1, 2006; 319(3): 1133 - 1143.
[Abstract] [Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
T. A. Lanz, M. J. Karmilowicz, K. M. Wood, N. Pozdnyakov, P. Du, M. A. Piotrowski, T. M. Brown, C. E. Nolan, K. E. G. Richter, J. E. Finley, et al.
Concentration-Dependent Modulation of Amyloid-beta in Vivo and in Vitro Using the {gamma}-Secretase Inhibitor, LY-450139
J. Pharmacol. Exp. Ther., November 1, 2006; 319(2): 924 - 933.
[Abstract] [Full Text] [PDF]


Home page
BrainHome page
C. L. Masters and K. Beyreuther
Alzheimer's centennial legacy: prospects for rational therapeutic intervention targeting the A{beta} amyloid pathway
Brain, November 1, 2006; 129(11): 2823 - 2839.
[Abstract] [Full Text] [PDF]


Home page
FASEB J.Home page
A. C. Nyborg, T. B. Ladd, K. Jansen, T. Kukar, and T. E. Golde
Intramembrane proteolytic cleavage by human signal peptide peptidase like 3 and malaria signal peptide peptidase
FASEB J, August 1, 2006; 20(10): 1671 - 1679.
[Abstract] [Full Text] [PDF]


Home page
FASEB J.Home page
F. Chen, E. A. Eckman, and C. B. Eckman
Reductions in levels of the Alzheimer's amyloid {beta} peptide after oral administration of ginsenosides
FASEB J, June 1, 2006; 20(8): 1269 - 1271.
[Abstract] [Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
J. D. Best, M. T. Jay, F. Otu, I. Churcher, M. Reilly, P. Morentin-Gutierrez, C. Pattison, T. Harrison, M. S. Shearman, and J. R. Atack
In Vivo Characterization of Abeta(40) Changes in Brain and Cerebrospinal Fluid Using the Novel {gamma}-Secretase Inhibitor N-[cis-4-[(4-Chlorophenyl)sulfonyl]-4-(2,5-difluorophenyl)cyclohexyl]-1,1,1-trifluoromethanesulfonamide (MRK-560) in the Rat
J. Pharmacol. Exp. Ther., May 1, 2006; 317(2): 786 - 790.
[Abstract] [Full Text] [PDF]


Home page
Cancer Res.Home page
M. Reedijk, S. Odorcic, L. Chang, H. Zhang, N. Miller, D. R. McCready, G. Lockwood, and S. E. Egan
High-level Coexpression of JAG1 and NOTCH1 Is Observed in Human Breast Cancer and Is Associated with Poor Overall Survival
Cancer Res., September 15, 2005; 65(18): 8530 - 8537.
[Abstract] [Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
J. D. Best, M. T. Jay, F. Otu, J. Ma, A. Nadin, S. Ellis, H. D. Lewis, C. Pattison, M. Reilly, T. Harrison, et al.
Quantitative Measurement of Changes in Amyloid-{beta}(40) in the Rat Brain and Cerebrospinal Fluid following Treatment with the {gamma}-Secretase Inhibitor LY-411575 [N2-[(2S)-2-(3,5-Difluorophenyl)-2-hydroxyethanoyl]-N1-[(7S)-5-methyl-6-oxo-6,7-dihydro-5H-dibenzo[b,d]azepin-7-yl]-L-alaninamide]
J. Pharmacol. Exp. Ther., May 1, 2005; 313(2): 902 - 908.
[Abstract] [Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
D. M. Barten, V. L. Guss, J. A. Corsa, A. Loo, S. B. Hansel, M. Zheng, B. Munoz, K. Srinivasan, B. Wang, B. J. Robertson, et al.
Dynamics of {beta}-Amyloid Reductions in Brain, Cerebrospinal Fluid, and Plasma of {beta}-Amyloid Precursor Protein Transgenic Mice Treated with a {gamma}-Secretase Inhibitor
J. Pharmacol. Exp. Ther., February 1, 2005; 312(2): 635 - 643.
[Abstract] [Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
T. A. Lanz, G. J. Fici, and K. M. Merchant
Lack of Specific Amyloid-{beta}(1-42) Suppression by Nonsteroidal Anti-Inflammatory Drugs in Young, Plaque-Free Tg2576 Mice and in Guinea Pig Neuronal Cultures
J. Pharmacol. Exp. Ther., January 1, 2005; 312(1): 399 - 406.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
A. C. Nyborg, K. Jansen, T. B. Ladd, A. Fauq, and T. E. Golde
A Signal Peptide Peptidase (SPP) Reporter Activity Assay Based on the Cleavage of Type II Membrane Protein Substrates Provides Further Evidence for an Inverted Orientation of the SPP Active Site Relative to Presenilin
J. Biol. Chem., October 8, 2004; 279(41): 43148 - 43156.
[Abstract] [Full Text] [PDF]




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
All ASPET Journals Molecular Pharmacology Pharmacological Reviews
 Molecular Interventions Drug Metabolism and Disposition

Copyright © 2004 by the American Society for Pharmacology and Experimental Therapeutics.