Cheung Zelda H, Leung Mason C P, Yip Henry K, Wu Wutian, Siu Flora K W, So Kwok-Fai
Department of Anatomy, Li Ka Shing Faculty of Medicine, The University of Hong Kong, 1/F, Laboratory block, 21 Sassoon Road, Pokfulam, Hong Kong, China.
Cell Mol Neurobiol. 2008 Jan;28(1):137-55. doi: 10.1007/s10571-007-9175-8. Epub 2007 Aug 21.
It was previously demonstrated that Menta-FX, a mixture of Panax quinquefolius L. (PQE), Ginkgo biloba (GBE), and Hypericum perforatum extracts (HPE), enhances retinal ganglion cell survival after axotomy. However, the mechanisms of neuroprotection remain unknown. The aim of this study is to elucidate the neuroprotective mechanisms of Menta-FX. Since PQE, GBE and HPE have all been observed to display anti-oxidative property, the involvement of anti-oxidation in Menta-FX's neuroprotective effect was investigated. Menta-FX lowered nitric oxide (NO) content in axotomized retinas without affecting nitric oxide synthase activity, suggesting that Menta-FX possibly exhibited a NO scavenging property. In addition, the effect of Menta-FX on the frequency of axotomy-induced nuclear fragmentation and caspase-3 activation was investigated. Menta-FX treatment significantly reduced nuclear fragmentation in axotomized retinas. Surprisingly, Menta-FX had no effect on caspase-3 activation, but selectively lowered caspase-3-independent nuclear fragmentation in axotomized retinal ganglion cells. In addition, inhibition of PI3K activity by intravitreal injection of wortmannin, a phosphoinositide-3 kinase (PI3K) inhibitor, completely abolished the neuroprotective effect of Menta-FX, indicating that Menta-FX's neuroprotective effect was PI3K-dependent. Data here suggest that Menta-FX displayed a PI3K-dependent, selective inhibition on a caspase-3-independent apoptotic pathway in axotomized RGCs, thus, highlighting the potential use of herbal remedies as neuroprotective agents for other neurodegenerative diseases.
先前的研究表明,Menta-FX(一种由西洋参(PQE)、银杏(GBE)和贯叶连翘提取物(HPE)组成的混合物)可提高视网膜神经节细胞在轴突切断后的存活率。然而,神经保护的机制尚不清楚。本研究的目的是阐明Menta-FX的神经保护机制。由于已观察到PQE、GBE和HPE均具有抗氧化特性,因此研究了抗氧化作用在Menta-FX神经保护作用中的参与情况。Menta-FX降低了轴突切断视网膜中的一氧化氮(NO)含量,而不影响一氧化氮合酶活性,这表明Menta-FX可能具有清除NO的特性。此外,研究了Menta-FX对轴突切断诱导的核碎裂频率和半胱天冬酶-3激活的影响。Menta-FX处理显著减少了轴突切断视网膜中的核碎裂。令人惊讶的是,Menta-FX对半胱天冬酶-3激活没有影响,但选择性地降低了轴突切断的视网膜神经节细胞中不依赖半胱天冬酶-3的核碎裂。此外,通过玻璃体内注射渥曼青霉素(一种磷酸肌醇-3激酶(PI3K)抑制剂)抑制PI3K活性,完全消除了Menta-FX的神经保护作用,表明Menta-FX的神经保护作用依赖于PI3K。这里的数据表明,Menta-FX对轴突切断的视网膜神经节细胞中不依赖半胱天冬酶-3的凋亡途径表现出PI3K依赖性的选择性抑制,因此,突出了草药作为其他神经退行性疾病神经保护剂的潜在用途。