The Neuroprotective Effects of Decursin Isolated from Angelica gigas Nakai Against Amyloid β-Protein-Induced Apoptosis in PC 12 Cells via a Mitochondria-Related Caspase Pathway

Neurochemical Research - Tập 40 - Trang 1555-1562 - 2015
Li Li1, Jikun Du2, Liyi Zou3, Haishan Xia3, Tie Wu3, Yongho Kim4, Yongwoo Lee4
1Dongguan Scientific Research Center, Guangdong Medical University, Dongguan, China
2Department of Clinical Laboratory, Shenzhen Shajing Affiliated Hospital of Guangzhou Medical University, Shenzhen, China
3Department of Pharmacology, Guangdong Medical University, Dongguan, China
4Department of Smart Food and Drugs, Graduate School, Inje University, Gimhae, South Korea

Tóm tắt

Decursin, purified from Angelica gigas Nakai, has been proven to exert neuroprotective property. Previous study revealed decursin protected the PC12 cells from Aβ25–35-induced oxidative cytotoxicity. The present study aimed to investigate whether decursin could protect PC12 cells from apoptosis caused by Aβ. Our results indicated that pretreatment of PC12 cells with decursin significantly inhibited Aβ25–35-induced cytotoxicity and apoptosis. The mechanism of action is likely to reverse Aβ25–35-induced mitochondrial dysfunction, including the reduction of mitochondrial membrane potential, the inhibition of reactive oxygen species production, and the decrease of mitochondrial release of cytochrome c in PC12 cells. In addition, decursin significantly suppressed the activity of caspase-3 and moderated the ratio of Bcl-2/Bax induced by Aβ25–35. These findings indicate that decursin exerts a neuroprotective effect against Aβ25–35-induced neurotoxicity in PC12 cells, at least in part, via suppressing the mitochondrial pathway of cellular apoptosis.

Tài liệu tham khảo

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