4.4 Article

Curcumin protects against doxorubicin induced oxidative stress by regulating the Keap1-Nrf2-ARE and autophagy signaling pathways

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PSYCHOPHARMACOLOGY
卷 240, 期 5, 页码 1179-1190

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SPRINGER
DOI: 10.1007/s00213-023-06357-z

关键词

CUR; DOX; Autophagy; Keap1-Nrf2-ARE; Oxidative stress

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Doxorubicin-induced neurotoxicity has been widely reported, and oxidative stress plays a critical role in this process. Curcumin has been shown to alleviate depressive-like state by mitigating oxidative stress and activating Nrf2-ARE signaling pathway. However, the exact mechanism of Curcumin in alleviating Doxorubicin-induced neurotoxicity is still unknown.
BackgroundDoxorubicin (DOX)-induced neurotoxicity is widely reported in previous studies. Oxidative stress has been validated as a critical event involved in DOX-induced neurotoxicity. As a selective autophagy adaptor protein, p62 is reported to regulate Keap1-Nrf2-ARE antioxidant pathway in response to oxidative stress. Curcumin (CUR) relieves depressive-like state through the mitigation of oxidative stress and the activation of Nrf2-ARE signaling pathway. However, the exact mechanism of CUR in alleviating DOX-induced neurotoxicity is still unknown.Materials and methodsThe rats were randomly divided into three groups: control group, DOX group, and DOX + CUR group. At the end of 3 weeks, the behavior tests as sucrose preference test (SPT), forced swimming test (FST), and novelty-suppressed feeding test (NSFT) were performed to assess anxiety- and depression-like behaviors. The rats were sacrificed after behavior tests, and the brain tissues were collected for biochemical analysis.ResultsIt was observed that the administration of CUR could effectively reverse DOX-induced depressive-like behaviors. The exposure of DOX activated autophagy and increased oxidative stress levels, and the administration of CUR could significantly inhibit DOX-induced autophagy and suppress oxidative stress. More importantly, we also found that Keap1-Nrf2-ARE signaling pathway was involved in DOX-induced neurotoxicity and oxidative stress regulated by autophagy.ConclusionOur study demonstrated that CUR could effectively reverse DOX-induced neurotoxicity through suppressing autophagy and mitigating oxidative stress and endoplasmic reticulum (ER) stress.

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