期刊
PHARMACOLOGICAL REPORTS
卷 72, 期 6, 页码 1604-1613出版社
SPRINGER HEIDELBERG
DOI: 10.1007/s43440-020-00116-z
关键词
Curcumin; Liver metabolism; beta-amyloid; APP(swe)/PS1(dE9) transgenic mice; Alzheimer's disease
资金
- Zhejiang Provincial Natural and Science Fund [LQ19F010003]
- Ningbo Natural and Science Fund [2019A610355]
Background An increasing number of studies have shown that Alzheimer's disease (AD) is a systemic disease characterized by brain dysfunction. In this study, we aimed to investigate the effects of curcumin on the liver, an important metabolic organ, and on the brain in APP(swe)/PS1(dE9)(APP/PS1) mice, and the interaction between these effects. Methods Curcumin was administered to 5-month-old APP/PS1 transgenic mice for 7 consecutive days using the intragastric (ig) and intracerebroventricular (icv) administration routes, respectively. The object recognition test (ORT) and open field test (OFT) were conducted to evaluate long-term recognition memory and anxiety after curcumin administration. Levels of beta-amyloid (A beta), A beta(42), and interleukin-1 beta (IL-1 beta) in the brain and liver were measured. Results In the ig group, curcumin ameliorated anxiety-like behavior and suppressed the level of A beta(42) in the liver and the total A beta in the brain. In the icv group, curcumin treatment affected the distribution of A beta(42) and IL-1 beta in the brain compared to the liver. There was a significant treatment-region interaction in A beta(42) level for the icv group (F(1, 24) = 17.7,p < 0.001), but no interaction effect for the ig group. Conclusion Our findings show that curcumin administration before A beta deposition shows promise for preventing AD, and further that curcumin may play an important role in the clearance of A beta(42) from the brain to the peripheral circulation.
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