4.5 Article

Caffeine Suppresses Amyloid-β Levels in Plasma and Brain of Alzheimer's Disease Transgenic Mice

期刊

JOURNAL OF ALZHEIMERS DISEASE
卷 17, 期 3, 页码 681-697

出版社

IOS PRESS
DOI: 10.3233/JAD-2009-1071

关键词

Alzheimer's disease; amyloid-beta; brain interstitial fluid; caffeine; plasma; transgenic mice

资金

  1. NIA-designated Florida Alzheimer's Disease Research Cente [P50AG025711, AG029524, AG13956]
  2. Cure Alzheimer's Fund
  3. Byrd Alzheimer's Center & Research Institute

向作者/读者索取更多资源

Recent epidemiologic studies suggest that caffeine may be protective against Alzheimer's disease (AD). Supportive of this premise, our previous studies have shown that moderate caffeine administration protects/restores cognitive function and suppresses brain amyloid-beta (A beta) production in AD transgenic mice. In the present study, we report that acute caffeine administration to both young adult and aged AD transgenic mice rapidly reduces A beta levels in both brain interstitial fluid and plasma without affecting A beta elimination. Long-term oral caffeine treatment to aged AD mice provided not only sustained reductions in plasma A beta, but also decreases in both soluble and deposited A beta in hippocampus and cortex. Irrespective of caffeine treatment, plasma A beta levels did not correlate with brain A beta levels or with cognitive performance in individual aged AD mice. Although higher plasma caffeine levels were strongly associated with lower plasma A beta(1-40) levels in aged AD mice, plasma caffeine levels were also not linked to cognitive performance. Plasma caffeine and theophylline levels were tightly correlated, both being associated with reduced inflammatory cytokine levels in hippocampus. Our conclusion is two-fold: first, that both plasma and brain A beta levels are reduced by acute or chronic caffeine administration in several AD transgenic lines and ages, indicating a therapeutic value of caffeine against AD; and second, that plasma A beta levels are not an accurate index of brain A beta levels/deposition or cognitive performance in aged AD mice.

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