Sex‐dependent cholinergic effects on amyloid pathology: A translational study

Author:

German‐Castelan Liliana12,Shanks Hayley R. C.2,Gros Robert134,Saito Takashi56,Saido Takaomi C.6,Saksida Lisa M.1247,Bussey Timothy J.1247,Prado Marco A. M.12478,Schmitz Taylor W.1279,Prado Vania F.12478,

Affiliation:

1. Robarts Research Institute Schulich School of Medicine and Dentistry University of Western Ontario London Ontario Canada

2. Neuroscience program Schulich School of Medicine and Dentistry University of Western Ontario London Ontario Canada

3. Department of Medicine Schulich School of Medicine & Dentistry University of Western Ontario London Ontario Canada

4. Department of Physiology and Pharmacology Schulich School of Medicine & Dentistry University of Western Ontario London Ontario Canada

5. Department of Neurocognitive Science Institute of Brain Science Nagoya City University Graduate School of Medical Sciences Nagoya Japan

6. Laboratory for Proteolytic Neuroscience RIKEN Center for Brain Science Wako, Saitama Japan

7. Western Institute for Neuroscience University of Western Ontario London Ontario Canada

8. Department of Anatomy and Cell Biology Schulich School of Medicine & Dentistry University of Western Ontario London Ontario Canada

9. Lawson Health Research Institute St. Joseph's Hospital London Ontario Canada

Abstract

AbstractINTRODUCTIONAbout two‐thirds of Alzheimer's Disease (AD) patients are women, who exhibit more severe pathology and cognitive decline than men. Whether biological sex causally modulates the relationship between cholinergic signaling and amyloid pathology remains unknown.METHODSWe quantified amyloid beta (Aβ) in male and female App‐mutant mice with either decreased or increased cholinergic tone and examined the impact of ovariectomy and estradiol replacement in this relationship. We also investigated longitudinal changes in basal forebrain (cholinergic function) and Aβ in elderly individuals.RESULTSWe show a causal relationship between cholinergic tone and amyloid pathology in males and ovariectomized female mice, which is decoupled in ovary‐intact and ovariectomized females receiving estradiol. In elderly humans, cholinergic loss exacerbates Aβ.DISCUSSIONOur findings emphasize the importance of reflecting human menopause in mouse models. They also support a role for therapies targeting estradiol and cholinergic signaling to reduce Aβ.Highlights Cholinergic tone regulates amyloid beta (Aβ) pathology in males and ovariectomized female mice. Estradiol uncouples the relationship between cholinergic tone and Aβ. In elderly humans, cholinergic loss correlates with increased Aβ in both sexes.

Funder

Canadian Institutes of Health Research

Publisher

Wiley

Subject

Psychiatry and Mental health,Cellular and Molecular Neuroscience,Geriatrics and Gerontology,Neurology (clinical),Developmental Neuroscience,Health Policy,Epidemiology

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