Crocin drives intestinal microbiota variation in a rat model of Alzheimer's disease by reducing DKK3 expression.

Background: Alzheimer's disease (AD) is a common neurodegenerative disease. Targeting DKK3-mediated intestinal microbiota (IM) variation is a promising strategy to treat AD. Crocin can alter IM distribution and inhibit DKK3 expression. We aimed to explore whether Crocin alleviates AD by regulating DKK3-mediated IM variation.

Methods: AD animal models were established by injecting Aβ into the brains of rats. Subsequently, AD rats were overexpressed with DKK3 and treated with Crocin. Morris water maze and passive avoidance tests were performed to assess the learning and memory abilities of the rats. The effect of Crocin on brain Aβ and p-tau levels, serum proinflammatory cytokine (TNF-α, IL-1β and IL-6) levels were analyzed. Then, hippocampal pathological damage of the rats was evaluated. Furthermore, DKK3, NeuN, Bax, BCL-2 expressions and GSK-3β phosphorylation were measured by immunohistochemistry and Western blot. Moreover, rat feces were collected for 16S rRNA sequencing.

Results: Crocin improved learning and memory abilities of AD rats. Additionally, Crocin inhibited brain Aβ and p-tau levels, and serum proinflammatory cytokine levels for AD rats. It was also observed that Crocin attenuated hippocampal pathological damage, inhibited DKK3, Bax expressions and GSK-3β phosphorylation, but increased NeuN, BCL-2 expressions for AD rats. Notably, Crocin increased the α and β diversity of the IM in AD rats. However, DKK3 overexpression reversed these situations. Additionally, Crocin treatment led to an increase in Prevotellaceae_NK3B31_group, alongside reductions in Lachnospiraceae UCG-001 and Family_XIII_AD3011_group.

Conclusion: Crocin alleviated AD by regulating DKK3-mediated IM variation, suggesting that DKK3-mediated IM variation was a potential therapeutic target for AD.