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Bilobalide prevents apoptosis through activation of the PI3K/Akt pathway in SH-SY5Y cells

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Abstract

Bilobalide, a sesquiterpene trilactone constituent of Ginkgo biloba leaf extracts, has been proposed to exert protective and trophic effects on neurons. However, mechanisms underlying the protective effects of bilobalide remain unclear. Using human SH-SY5Y neuroblastoma cells and primary hippocampal neurons, this study investigated the neuroprotective effects of bilobalide. We mimicked aging-associated neuronal impairments by applying external factors (beta amyloid protein (Aβ) 1-42, H2O2 and serum deprivation) consequently inducing cell apoptosis. As markers for apoptosis, cell viability, DNA fragmentation, mitochondrial membrane potential and levels of cleaved caspase 3 were measured. We found that, bilobalide prevented Aβ 1-42-, H2O2- and serum deprivation-induced apoptosis. To better understand the neuroprotective effects of bilobalide, we also tested the ability of bilobalide to modulate pro-survival signaling pathways such as protein kinase C (PKC), extracellular-regulated kinase 1/2 (ERK1/2) and phosphatidylinositol 3-kinase (PI3K)/Akt pathways. It was found that, bilobalide dose-dependently increased PI3K activity and levels of phosphorylated Akt (p-Akt Ser473 and Thr308), which could be maintained up to at least 2 h after bilobalide withdrawal in cells treated with or without Aβ 1-42, H2O2 or serum-free medium. In addition, application of PI3K/Akt inhibitor LY294002 could abrogate both the protective effects of bilobalide against Aβ 1-42-, H2O2- and serum deprivation-induced apoptotic cell damage and bilobalide-induced increase in PI3K activity and levels of p-Akt (Ser473 and Thr308). In contrast, application of PKC inhibitor staurosporine (STS) did not affect the protective effects of bilobalide. Moreover, no change in levels of phosphorylated ERK1/2 (p-ERK1/2) was observed in bilobalide-treated cells. These results further suggested that the PI3K/Akt pathway might be involved in the protective effects of bilobalide. Since modern technology allows production of purified bilobalide with high bioavailability, bilobalide may be useful in developing therapy for diseases involving age-associated neurodegeneration.

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Acknowledgments

Many thanks for support from the GuangDong Provincial Natural Science Foundation (No. 20090171110046) and Science Foundation of Ministry of Education of China (No. 9151008901000039).

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Authors and Affiliations

  1. Department of Anatomy, Zhongshan School of Medicine, Sun Yat-Sen University Guangzhou, Guangdong, 510080, China

    Chun Shi, Fengming Wu & Jie Xu

  2. Department of Anatomy, The Chinese University of Hong Kong, Shatin, NT, Hong Kong

    Chun Shi & David T. Yew

  3. Department of Histology and Embryology, Zhongshan School of Medicine, Sun Yat-Sen University Guangzhou, Guangdong, 510080, China

    Yonghong Zhu

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  1. Chun Shi
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Correspondence to Yonghong Zhu.

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Chun Shi and Fengming Wu contribute to this work equally and are listed as co-first authors.

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Shi, C., Wu, F., Yew, D.T. et al. Bilobalide prevents apoptosis through activation of the PI3K/Akt pathway in SH-SY5Y cells. Apoptosis 15, 715–727 (2010). https://doi.org/10.1007/s10495-010-0492-x

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