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It is generally believed that copper deposition can induce apoptosis through endoplasmic reticulum stress, mitochondrial autophagy, and oxidative stress ( in vitro studies have shown that copper stress mainly causes copper death rather than apoptosis and iron death, more in vivo studies, including our study, have shown that apoptosis and other death modes exist simultaneously in vivo

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NPs can cross the BBB and deliver the BDNF to the brain, thereby increasing the bioavailability of BDNF in the brain

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