Caffeine protects against oxidative stress and Alzheimer's disease-like pathology in rabbit hippocampus induced by cholesterol-enriched diet

• Published in: Free radical biology & medicine 2010-10, Vol.49 (7), p.1212-1220
• Main Authors: Prasanthi, Jaya R.P., Dasari, Bhanu, Marwarha, Gurdeep, Larson, Tyler, Chen, Xuesong, Geiger, Jonathan D., Ghribi, Othman
• Format: Article
• Language: English
• Subjects: Adenosine receptors; Alzheimer Disease - drug therapy; Alzheimer Disease - etiology; Alzheimer Disease - metabolism; Alzheimer's disease; Amyloid - biosynthesis; Amyloid - genetics; Animals; Caffeine; Caffeine - administration & dosage; Cholesterol; Cholesterol, Dietary - adverse effects; Cytoprotection; Disease Models, Animal; Endoplasmic Reticulum - drug effects; Endoplasmic Reticulum - metabolism; Endoplasmic reticulum stress; Free radicals; Hippocampus - drug effects; Hippocampus - metabolism; Hippocampus - pathology; Humans; Male; Oxidative stress; Oxidative Stress - drug effects; Rabbits; Reactive Oxygen Species - metabolism; Receptor, Adenosine A1 - biosynthesis; Receptor, Adenosine A1 - genetics; Tau; tau Proteins - metabolism; β-Amyloid
• ISSN: 0891-5849; 1873-4596
• DOI: 10.1016/j.freeradbiomed.2010.07.007

Cholesterol has been linked to the pathogenesis of sporadic Alzheimer's disease (AD) as a risk factor increasing β-amyloid (Aβ) and oxidative stress levels. Caffeine has antioxidant properties and has been demonstrated to reduce Aβ levels in transgenic mouse models of familial AD. However, the effects of caffeine on cholesterol-induced sporadic AD pathology have not been determined. In this study, we determined the effects of caffeine on Aβ levels, tau phosphorylation, oxidative stress generation, and caffeine-target receptors in rabbits fed a 2% cholesterol-enriched diet, a model system for sporadic AD. Our results showed that the cholesterol-enriched diet increased levels of Aβ, tau phosphorylation, and oxidative stress measured as increased levels of reactive oxygen species and isoprostanes, glutathione depletion, and increased levels of endoplasmic reticulum stress marker proteins. Additionally, the cholesterol-enriched diet reduced the levels of adenosine A 1 receptors (A 1R) but not ryanodine or adenosine A 2A receptors. Caffeine, administered at 0.5 and 30 mg/day in the drinking water, reduced the cholesterol-induced increase in Aβ, phosphorylated tau, and oxidative stress levels and reversed the cholesterol-induced decrease in A 1R levels. Our results suggest that even very low doses of caffeine might protect against sporadic AD-like pathology.