EGb761 Ameliorates Neuronal Apoptosis and Promotes Angiogenesis in Experimental Intracerebral Hemorrhage via RSK1/GSK3β Pathway
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Abstract
Neuronal apoptosis after intracerebral hemorrhage (ICH) plays an essential role in neurological deterioration. Preclinical studies have shown that EGb761, an extract of Ginkgo biloba, is neuroprotective in some other neurological diseases with apoptosis. This study was conducted to investigate the potential neuroprotective effect of EGb761 on neuronal apoptosis in experimental ICH. A model of ICH was induced in C57BL/6 mice by injecting collagenase. EGb761 was administered for 21 days and neurologic behaviors were assessed at 1, 3, 7, 14, and 21 days after ICH. RNAi-mediated knockdown of p90 ribosomal S6 kinase 1 (RSK1) was used to further investigate the role of RSK1 in EGb761-induced neuroprotective effects. Neuronal death was determined by TUNEL staining. The image datasets of neurovascular networks were acquired via micro-optical sectioning tomography (MOST). The glycogen synthase kinase-3β (GSK3β) activity was assayed using commercial kit. Primary cultured cortical neurons were exposed to ferrous iron and treated with EGb761. Apoptotic neurons were counted by flow cytometry. RSK1, GSK3β, phosphorylated-GSK3β (pGSK3β), Bcl2, Bax, cleaved-caspase3 (CC3), and VEGF were measured by Western blot. The pGSK3β was also detected by immunofluorescence staining. We found that mice in EGb761 group performed better on rotarod test. Reduced TUNEL-positive neurons and richer microvascular networks were observed in mice treated with EGb761. EGb761 attenuates neuronal apoptosis induced by ferrous iron counted by flow cytometry in vitro. Decreased GSK3β activity was observed in EGb761-treated mice compared with mice with ICH. EGb761 increased the expression of pGSK3β (Ser9), RSK1 and the Bcl2/Bax ratio, and VEGF and decreased CC3 expression. In conclusion, EGb761 reduces neuronal apoptosis and promotes angiogenesis in experimental intracerebral hemorrhage via RSK1/GSK3β pathway.
Keywords
Intracerebral hemorrhage Neuroprotection Glycogen synthase kinase-3 beta Apoptosis AngiogenesisNotes
Acknowledgements
This investigation was supported by Prof. Zhouping Tang’s National Natural Science Foundation of China (81171089, 81471211). We would like to express our gratitude to Dr. Teng Zhang for his assistance in this experiment.
We are very grateful to Wuhan Oebio Biology Co., Ltd. (http://www.oebio.com/) for kindly assisting us with the MOST technique used in the reconstruction of 3D neurovascular networks. Ginkgo biloba (EGb761) was kindly provided by Dr. Willmar Schwabe Pharmaceuticals, Germany.
Authors’ Contributions
Chao Pan performed most of the experiments and drafted the manuscript; Na Liu and Ping Zhang conducted the neuronal culture studies; Qian Wu performed the flow cytometry; Hong Deng established the animal models; Feng Xu bred the mice and conducted the behavioral tests; Lifei Lian and Qiming Liang performed the Western blot; Yang Hu conducted the statistical analysis; and Prof. Zhouping Tang and Suiqiang Zhu designed and guided the experiments.
Compliance with Ethical Standards
Conflict of Interest
The authors declare that they have no competing interests.
Glossary
Alzheimer’s disease
Cleaved-caspase3
Glycogen synthase kinase-3β
Intracerebral hemorrhage
Modified neurological severity score
Micro-optical sectioning tomography
Parkinson’s disease
Phosphorylated-GSK3β
Propidium iodide
RNA interference
p90 ribosomal S6 kinase 1
Subarachnoid hemorrhage
Supplementary material
References
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