Diet, Genomics, and Immunology Laboratory, Beltsville Human Nutrition Research Center, Agricultural Research Service, United States Department of Agriculture, Beltsville, MD 20705, USA.
Neuroscience. 2011 Jun 2;183:1-14. doi: 10.1016/j.neuroscience.2011.03.064. Epub 2011 Apr 7.
The protective effects of the flavonoid polyphenols, myricetin and quercetin, were investigated on key features of ischemic injury in cultures including cell swelling and the reduction in glutamate uptake. C6 glial cells were exposed to oxygen-glucose deprivation (OGD) for 5 h and cell swelling was determined 90 min after the end of OGD. OGD-induced swelling was significantly blocked by both quercetin and myricetin although higher concentrations were required for quercetin. OGD-induced free radical production, a contributing factor in cell swelling, was significantly reduced by both myricetin and quercetin. However, depolarization of the inner mitochondrial membrane potential (ΔΨ(m)), the blockade of which generally reduces swelling, was significantly diminished by myricetin, but not quercetin. This indicated that quercetin could reduce swelling despite its inability to prevent depolarization of ΔΨ(m) possibly through other signaling pathways. Increased intracellular calcium (Ca²+) is an important characteristic of ischemic injury and is implicated in swelling. Both myricetin and quercetin attenuated the increase in Ca²+. Further, a reduction in Ca²+, through the use of nifedipine, nimodipine, verapamil, dantrolene, or BAPTA-AM, significantly reduced OGD-induced cell swelling indicating that one possible mechanism by which such flavonoids attenuate cell swelling may be through regulating Ca²+. OGD-induced decrease in glutamate uptake was attenuated by myricetin, but not quercetin. Cyclosporin A, a blocker of the mitochondrial permeability transition (mPT) pore, but not FK506 (that does not block the mPT), attenuated the decline in glutamate uptake after OGD, indicating the involvement of the mPT in glutamate uptake. Our results indicated that while blockade of ΔΨ(m) may be sufficient to reduce swelling, it may not be a necessary factor, and that flavonoids reduce cell swelling by regulating Ca²+. The differential effects of myricetin and quercetin on OGD-induced reduction on glutamate uptake may be due to their differential effects on mitochondria.
研究了类黄酮多酚杨梅素和槲皮素对包括细胞肿胀和谷氨酸摄取减少在内的缺血性损伤关键特征的保护作用。将 C6 神经胶质细胞暴露于氧葡萄糖剥夺(OGD)中 5 小时,并在 OGD 结束后 90 分钟测定细胞肿胀。尽管需要更高浓度的 quercetin,但 quercetin 和 myricetin 均可显著阻断 OGD 诱导的肿胀。OGD 诱导的自由基产生,这是细胞肿胀的一个促成因素,也被 myricetin 和 quercetin 显著降低。然而,线粒体内膜电位(ΔΨ(m))的去极化,一般可减少肿胀,myricetin 显著减弱,但 quercetin 没有。这表明 quercetin 可以减少肿胀,尽管它不能防止 ΔΨ(m)的去极化,可能通过其他信号通路。细胞内钙离子([Ca²+](i))的增加是缺血性损伤的一个重要特征,与肿胀有关。myricetin 和 quercetin 均减弱了[Ca²+](i)的增加。此外,通过使用硝苯地平、尼莫地平、维拉帕米、丹曲林或 BAPTA-AM 降低[Ca²+](i),可显著降低 OGD 诱导的细胞肿胀,表明这些类黄酮减轻细胞肿胀的一种可能机制可能是通过调节[Ca²+](i)。OGD 诱导的谷氨酸摄取减少被 myricetin 减弱,但 quercetin 没有。环孢菌素 A(一种线粒体通透性转换(mPT)孔的阻断剂),而不是 FK506(不阻断 mPT),减弱了 OGD 后谷氨酸摄取的下降,表明 mPT 参与了谷氨酸摄取。我们的结果表明,虽然阻断ΔΨ(m)可能足以减少肿胀,但它可能不是一个必要因素,类黄酮通过调节[Ca²+](i)来减少细胞肿胀。myricetin 和 quercetin 对 OGD 诱导的谷氨酸摄取减少的不同影响可能是由于它们对线粒体的不同影响。