Correction: treatment with bexarotene, a compound that increases apolipoprotein-E, provides no cognitive benefit in mutant APP/PS1 mice
نویسندگان
چکیده
Correction to LaClair et al.: Treatment with bexarotene, a compound that increases apolipoprotein-E, provides no cognitive benefit in mutant APP/PS1 mice. Molecular Neurodegeneration 2013 8:18. After publication of this work [1], we were alerted to an error in the reported cohort size used for the Radial Arm Water Maze as referenced from [2]. The correct cohort size reported in [2] is n=8-13 for each group of mixed gender animals. In addition, it came to our attention that our analysis of a potential false-positive treatment effect caused by gender differences, and therefore bexarotene’s inability to rescue cognitive decline, may appear to be contradicted by the statement that it “was equally effective in both genders” of transgenic mice [2]. However, direct experimental data supporting this statement is not presented. In addition, this statement does not address any differences in the performance of each gender, only that bexarotene appears effective in each gender separately, and the statistical significance of this reported effect remains unknown. Therefore, we maintain that the currently published cognitive preclinical data, including our own, do not validate the potential of bexarotene for Alzheimer’s therapy.”
منابع مشابه
Comment on “ApoE-Directed Therapeutics Rapidly Clear b-Amyloid and Reverse Deficits in AD Mouse Models”
ApoE4 is the most important genetic risk factor for Alzheimer’s disease (AD) (1), and we therefore read with great interest the paper by Cramer et al. (2) demonstrating spectacular results of bexarotene on b-amyloid (Ab) accumulation in the brain of mouse models for AD. Bexarotene is a retinoid X receptor (RXR) agonist and approved by the U.S. Food and Drug Administration (FDA) for treatment of...
متن کاملRXR controlled regulatory networks identified in mouse brain counteract deleterious effects of Aβ oligomers
Bexarotene, a selective agonist for Retinoid X receptors (RXR) improves cognitive deficits and amyloid-β (Aβ) clearance in mice. Here we examine if the effect of bexarotene on RXR cistrome and transcriptomes depend on APOE isoform and Aβ deposition. We found bexarotene increased RXR binding to promoter regions in cortex of APOE3 mice. Rho family GTPases and Wnt signaling pathway were highly enr...
متن کاملComment on "ApoE-directed therapeutics rapidly clear β-amyloid and reverse deficits in AD mouse models".
Cramer et al. (Reports, 23 March 2012, p. 1503; published online 9 February 2012) demonstrated in a mouse model for Alzheimer's disease (AD) that treatment of APP/PS1ΔE9 mice with bexarotene decreased Aβ pathology and ameliorated memory deficits. We confirm the reversal of memory deficits in APP/PS1ΔE9 mice expressing human APOE3 or APOE4 to the levels of their nontransgenic controls and the si...
متن کاملUltrastructural studies in APP/PS1 mice expressing human ApoE isoforms: implications for Alzheimer's disease.
Alzheimer's disease is characterized in part by extracellular aggregation of the amyloid-β peptide in the form of diffuse and fibrillar plaques in the brain. Electron microscopy (EM) has made an important contribution in understanding of the structure of amyloid plaques in humans. Classical EM studies have revealed the architecture of the fibrillar core, characterized the progression of neuriti...
متن کاملProgressive, age-related behavioral impairments in transgenic mice carrying both mutant amyloid precursor protein and presenilin-1 transgenes.
This study provides a comprehensive behavioral characterization during aging of transgenic mice bearing both presenilin-1 (PS1) and amyloid precursor protein (APP(670,671)) mutations. Doubly transgenic mice and non-transgenic controls were evaluated at ages wherein beta-amyloid (Abeta) neuropathology in APP+PS1 mice is low (5-7 months) or very extensive (15-17 months). Progressive cognitive imp...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره 8 شماره
صفحات -
تاریخ انتشار 2013