Title | Istradefylline reduces memory deficits in aging mice with amyloid pathology. |
Publication Type | Journal Article |
Year of Publication | 2018 |
Authors | Orr AG, Lo I, Schumacher H, Ho K, Gill M, Guo W, Kim DH, Knox A, Saito T, Saido TC, Simms J, Toddes C, Wang X, Yu G-Q, Mucke L |
Journal | Neurobiol Dis |
Volume | 110 |
Pagination | 29-36 |
Date Published | 2018 Feb |
ISSN | 1095-953X |
Abstract | Adenosine A receptors are putative therapeutic targets for neurological disorders. The adenosine A receptor antagonist istradefylline is approved in Japan for Parkinson's disease and is being tested in clinical trials for this condition elsewhere. A receptors on neurons and astrocytes may contribute to Alzheimer's disease (AD) by impairing memory. However, it is not known whether istradefylline enhances cognitive function in aging animals with AD-like amyloid plaque pathology. Here, we show that elevated levels of Aβ, C-terminal fragments of the amyloid precursor protein (APP), or amyloid plaques, but not overexpression of APP per se, increase astrocytic A receptor levels in the hippocampus and neocortex of aging mice. Moreover, in amyloid plaque-bearing mice, low-dose istradefylline treatment enhanced spatial memory and habituation, supporting the conclusion that, within a well-defined dose range, A receptor blockers might help counteract memory problems in patients with Alzheimer's disease. |
DOI | 10.1016/j.nbd.2017.10.014 |
Alternate Journal | Neurobiol. Dis. |
PubMed ID | 29100987 |
PubMed Central ID | PMC5747997 |
Grant List | P50 AG023501 / AG / NIA NIH HHS / United States R00 AG048222 / AG / NIA NIH HHS / United States P30 NS065780 / NS / NINDS NIH HHS / United States K99 AG048222 / AG / NIA NIH HHS / United States C06 RR018928 / RR / NCRR NIH HHS / United States |